Veracyte is a leading genomic diagnostics company that leverages advanced technology to provide accurate and reliable testing solutions for patients with suspicious nodules or lesions. Through their innovative molecular testing platforms, Veracyte helps healthcare providers make more informed decisions, leading to improved patient outcomes and reduced healthcare costs. With a strong focus on research and development, Veracyte continues to drive advancements in genomic testing to transform the field of diagnostic medicine.

At Veracyte, we offer exciting career opportunities for those interested in joining a pioneering team that is committed to transforming cancer care for patients across the globe. Working at Veracyte enables our employees to not only make a meaningful impact on the lives of patients, but to also learn and grow within a purpose driven&nbsp;environment. This is what we call the Veracyte way&nbsp;– it’s about how we work together, guided by our values, to give clinicians the insights they need to help patients make life-changing decisions.&nbsp; Our Values: We Seek A Better Way: We innovate boldly, learn from our setbacks, and are resilient in our pursuit to transform cancer care We Make It Happen: We act with urgency, commit to quality, and bring fun to our hard work We Are Stronger Together:&nbsp;We collaborate openly, seek to understand, and celebrate our wins We Care Deeply: We embrace our differences, do the right thing, and encourage each other &nbsp;&nbsp; The Position: The Genomic Specialist (GS) is the front line of Veracyte’s customer interaction.&nbsp; The GS identifies and closes new business while maintaining and growing existing business. The GS’s primary focus is to clinically reinforce the value of our diagnostic tests (Afirma plus Xpression Atlas) with new and existing customers to support implementation of routine collection and ordering protocols and procedures.&nbsp; The clinical promotion of our diagnostics tests will primarily take place in hospitals and office environments with a focus on engaging Endocrinologists, Pathologists, ENT’s, Surgeons, Radiologists, and medical staff.&nbsp; This position is covering the territory of Cleveland, OH. &nbsp; Essential duties &amp; responsibilities include:&nbsp; Become fluent in the clinical messaging, sample collection, ordering and shipping protocols, and reimbursement and coverage messaging related to our genomic diagnostic products Reinforce the value proposition of our genomic diagnostic products to our customers in a way that aligns with their health system and/or clinical practice goals of high-quality patient care Navigate complex health systems to reinforce our value proposition with all keys stakeholders that impact the use of our products, and prospect for business growth opportunities within and across product lines Take accountability and ownership of your accounts by developing strong and long-term relationships with clinical customers and medical staff such that you are viewed as a valued resource to the customer Analyze territory data to develop strategic plans and execute daily Establish clear and repeatable protocols within accounts for the collection and ordering of our genomic diagnostic products including guiding the clinical patient selection criteria, sample logistics and other hospital facility and medical staff processes as necessary Develop clear and actionable territory plans to exceed territory goals Work collaboratively with internal teammates to maintain and grow business across our testing portfolio Comply with all laws, regulations and policies that govern the conduct of Veracyte activities Business travel, by air or car, is regularly required. &nbsp;Overnights will be required &nbsp; Who You Are: You are motivated by the opportunity to contribute to the adoption of clinically vital diagnostic tests that dramatically improve patient outcome and quality of life. You have five to eight years in medical diagnostics, medical device, or biopharmaceuticals and a track record of meeting or exceeding goals.&nbsp; A Bachelor's degree or equivalent experience is required. Science based degrees in biology, chemistry or equivalent area is preferred. Additional experiences and demonstrated competencies include: Proven track record of successfully calling on complex health systems, IDNs, and Academic institutions with multi-key influencers Identify new opportunities to navigate through a complicated sales cycle resulting in new genomic test volume Aptitude to sell clinically in-person or virtually in an office or hospital environment History of maintaining and growing existing customer base in a large geography Experience managing multiple accounts and products Capacity to totally immerse into an account to assess stability and growth opportunity Ideally have sold and functioned in procedure environment Strong time management skills: effectively managing one’s time and resources to ensure that work is completed efficiently High business acumen: ability to prioritize and adapt to evolving business needs Collaborative team player: works cooperatively with others to help a team achieve its goals, proactively reaches out to partners, communicates and aligns on goals, priorities and roles &amp; responsibilities, follows up and courageously communicates and triages issues as they arise Strong communication skills: written, oral and presentation. Has an attention to detail Keeps the organization's vision and values at the forefront of daily actions &nbsp; #L1-Remote &nbsp;The final salary offered to a successful candidate will be dependent on several factors that may include but are not limited to the type and length of experience within the job, type and length of experience within the industry, education, etc. Base pay is one part of the Total Package that is provided to compensate and recognize employees for their work, and this role may be eligible for additional discretionary bonuses/incentives, and restricted stock units. Veracyte is a multi-state employer, and this salary range may not reflect positions that work in other states.Pay range$108,000&mdash;$120,000 USD&nbsp; What We Can Offer You Veracyte is a growing company that offers significant career opportunities if you are curious, driven, patient-oriented and aspire to help us build a great company. We offer competitive compensation and benefits, and are committed to fostering an inclusive workforce, where diverse backgrounds are represented, engaged, and empowered to drive innovative ideas and decisions. We are thrilled to be recognized as a 2024 Certified™ Great Place to Work® in both the US and Israel - a testament to our dynamic, inclusive, and inspiring workplace where passion meets purpose. &nbsp; About Veracyte Veracyte&nbsp;(Nasdaq: VCYT) is a global genomic diagnostics company that improves patient care by providing answers to clinical questions, informing diagnosis and treatment decisions throughout the patient journey in cancer and other diseases. The company’s growing menu of genomic tests leverage advances in genomic science and technology, enabling patients to avoid risky, costly diagnostic procedures and quicken time to appropriate treatment. The company’s tests in lung cancer, prostate cancer, breast cancer, thyroid cancer, bladder cancer and idiopathic pulmonary fibrosis are available to patients and its lymphoma subtyping and renal cancer tests are in development. With Veracyte’s exclusive global license to a best-in-class diagnostics instrument platform, the company is positioned to deliver its tests to patients worldwide.&nbsp;Veracyte&nbsp;is based in&nbsp;South San Francisco, California. For more information, please visit&nbsp;www.veracyte.com and follow the company on X (Formerly Twitter). Veracyte, Inc. is an Equal Opportunity Employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status or disability status. Veracyte participates in E-Verify in the United States. View our&nbsp;CCPA Disclosure Notice. If you receive any suspicious alerts or communications through LinkedIn or other online job sites for any position at Veracyte, please exercise caution and promptly report any concerns to careers@veracyte.com

Genomic Specialist - Cleveland, OH

At Veracyte, we offer exciting career opportunities for those interested in joining a pioneering team that is committed to transforming cancer care for patients across the globe. Working at Veracyte enables our employees to not only make a meaningful impact on the lives of patients, but to also learn and grow within a purpose driven&nbsp;environment. This is what we call the Veracyte way&nbsp;– it’s about how we work together, guided by our values, to give clinicians the insights they need to help patients make life-changing decisions.&nbsp; Our Values: We Seek A Better Way: We innovate boldly, learn from our setbacks, and are resilient in our pursuit to transform cancer care We Make It Happen: We act with urgency, commit to quality, and bring fun to our hard work We Are Stronger Together:&nbsp;We collaborate openly, seek to understand, and celebrate our wins We Care Deeply: We embrace our differences, do the right thing, and encourage each other &nbsp;The Position: We are seeking a detail-oriented experienced Governance, Risk &amp; Compliance (GRC) Senior Analyst to assist with leading and supporting the organization’s governance, risk, and compliance initiatives. Under the direction of Management the incumbent will perform IT risk assessments, ensure controls, policies and procedures and resources are in place for IT and Security teams to effectively manage risk. You&nbsp;will articulate risk appetite and advocate risk culture; act as a challenge function by providing questions and feedback across multiple functions. In addition, you will&nbsp;ensure that the company’s operations align with relevant regulations, internal policies, standards and risk management frameworks. The ideal candidate will have a strong understanding of risk management principles, compliance standards, and information security best practices. As the program evolves the role will be responsible for maturing the GRC operations.&nbsp; Essential Responsibilities: Governance &amp; Compliance:&nbsp; Assist in developing and maintaining internal control frameworks, policies, and procedures that align with industry regulations (e.g., ISO 27001, SOX, GDPR, HIPAA).&nbsp; Ensure organizational compliance with legal and regulatory requirements.&nbsp; Monitor and report on compliance with data privacy regulations and internal security policies.&nbsp; Collaborate with departments to implement and improve governance processes.&nbsp; Track and report on GRC metrics, KPIs, and audit remediation activities&nbsp; Risk Management:&nbsp; Contribute to enhancing IT and Security risk management program&nbsp; Perform risk assessments, identifying vulnerabilities, threats, and control gaps.&nbsp; Conduct vendor risk management reviews, evaluating the risk posed by third-party service providers.&nbsp; Support the implementation of risk management frameworks and tools.&nbsp; Provide recommendations for mitigating identified risks and ensuring effective remediation strategies.&nbsp; Monitor and track risk treatment plans and risk acceptance decisions.&nbsp; Internal Audit Support:&nbsp; Assist in internal and external audits to ensure audit testing are conducted in a cooperative, timely efficient manner with value added reporting and cost effective recommendation being provide to management to strengthen IT and Security conrols.&nbsp; Conduct audits of high risk processes within IT and Security functions to ensure compliance with policies and standards.&nbsp; Work with IT process owners to identify/improve and document detail controls for key applications, security and infrastructure components relating to compliance with SOX, GDPR, HIPPA, ISO27000 etc.&nbsp; Provide periodic reports to leadership on open issues and remediation status.&nbsp; Establish and maintain IT and Cybersecurity risk register.&nbsp; Track audit findings in the appropriate risk and audit findings registers. Work with control owners to ensure findings are remediated on a timely basis.&nbsp; Incident Response:&nbsp; Assist in developing and improving the organization's incident response plan.&nbsp; Participate in incident investigations and support post-incident reviews to identify control weaknesses.&nbsp; Familiar with risk management and controls frameworks, cyber kill chain and NIST incident response lifecycle&nbsp; Document and define improvements over incident playbooks&nbsp; Perform root cause analysis and lessons learned reporting&nbsp; Maintain incident response tracker Training &amp; Awareness:&nbsp; Contribute to the development of security awareness training programs and conduct training sessions as needed.&nbsp; Ensure the organization’s Cybersecurity Training and Awareness program meets industry regulations, standards , and compliance requirements.&nbsp; Communicate changes in regulatory requirements and provide guidance on compliance best practices to employees.&nbsp; Who You Are: Bachelor’s degree in Information Security, Risk Management, Business Administration, or a related field.&nbsp; 5+ years of experience in GRC, information security, risk management, or compliance.&nbsp; Experience with regulatory frameworks such as ISO 27001, NIST, SOX, PCI-DSS, GDPR, HIPAA, etc.&nbsp; Experience in risk assessments and compliance audits is preferred.&nbsp; Strong knowledge of risk management and compliance frameworks.&nbsp; Familiarity with third-party vendor risk management practices.&nbsp; Excellent communication and report-writing skills.&nbsp; Detail-oriented with the ability to analyze complex regulatory requirements.&nbsp; Proficient in using GRC tools and software for tracking and managing compliance/risk activities.&nbsp; Ability to manage multiple projects and take on other security tasks as needed&nbsp; Certifications (Preferred):&nbsp; Certified Information Systems Auditor (CISA)&nbsp; Certified Information Security Manager (CISM)&nbsp; Certified Information Systems Security Professional (CISSP)&nbsp; Certified in Risk and Information Systems Control (CRISC)&nbsp; Certified Information Privacy Professional (CIPP)&nbsp; #LI-Remote &nbsp;The final salary offered to a successful candidate will be dependent on several factors that may include but are not limited to the type and length of experience within the job, type and length of experience within the industry, education, etc. Base pay is one part of the Total Package that is provided to compensate and recognize employees for their work, and this role may be eligible for additional discretionary bonuses/incentives, and restricted stock units. Veracyte is a multi-state employer, and this salary range may not reflect positions that work in other states.Pay range$140,000&mdash;$167,000 USD&nbsp; What We Can Offer You Veracyte is a growing company that offers significant career opportunities if you are curious, driven, patient-oriented and aspire to help us build a great company. We offer competitive compensation and benefits, and are committed to fostering an inclusive workforce, where diverse backgrounds are represented, engaged, and empowered to drive innovative ideas and decisions. We are thrilled to be recognized as a 2024 Certified™ Great Place to Work® in both the US and Israel - a testament to our dynamic, inclusive, and inspiring workplace where passion meets purpose. &nbsp; About Veracyte Veracyte&nbsp;(Nasdaq: VCYT) is a global genomic diagnostics company that improves patient care by providing answers to clinical questions, informing diagnosis and treatment decisions throughout the patient journey in cancer and other diseases. The company’s growing menu of genomic tests leverage advances in genomic science and technology, enabling patients to avoid risky, costly diagnostic procedures and quicken time to appropriate treatment. The company’s tests in lung cancer, prostate cancer, breast cancer, thyroid cancer, bladder cancer and idiopathic pulmonary fibrosis are available to patients and its lymphoma subtyping and renal cancer tests are in development. With Veracyte’s exclusive global license to a best-in-class diagnostics instrument platform, the company is positioned to deliver its tests to patients worldwide.&nbsp;Veracyte&nbsp;is based in&nbsp;South San Francisco, California. For more information, please visit&nbsp;www.veracyte.com and follow the company on X (Formerly Twitter). Veracyte, Inc. is an Equal Opportunity Employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status or disability status. Veracyte participates in E-Verify in the United States. View our&nbsp;CCPA Disclosure Notice. If you receive any suspicious alerts or communications through LinkedIn or other online job sites for any position at Veracyte, please exercise caution and promptly report any concerns to careers@veracyte.com

Governance, Risk & Compliance (GRC) Senior Analyst

At Veracyte, we offer exciting career opportunities for those interested in joining a pioneering team that is committed to transforming cancer care for patients across the globe. Working at Veracyte enables our employees to not only make a meaningful impact on the lives of patients, but to also learn and grow within a purpose driven&nbsp;environment. This is what we call the Veracyte way&nbsp;– it’s about how we work together, guided by our values, to give clinicians the insights they need to help patients make life-changing decisions.&nbsp; Our Values: We Seek A Better Way: We innovate boldly, learn from our setbacks, and are resilient in our pursuit to transform cancer care We Make It Happen: We act with urgency, commit to quality, and bring fun to our hard work We Are Stronger Together:&nbsp;We collaborate openly, seek to understand, and celebrate our wins We Care Deeply: We embrace our differences, do the right thing, and encourage each other &nbsp;The Position: The Manager, Cytology is responsible for overseeing the daily operations of the laboratory to ensure efficiency, quality, and compliance with all regulatory standards and corporate policies. This role provides direct supervision to staff, manages workflow, and support continuous improvement initiatives to meet TAT, KPI, and quality goals. The Manager, Cytology assumes operational responsibility in the Manager’s absence, ensuring seamless lab operations and adherence to organizational standards. This is an onsite position, based in our Austin Laboratory. We are also open to relocation for the ideal candidate. The schedule for Manager, Cytology is Tues - Sat, 9:30am – 6:00pm. Flexibility to adjust schedule, including weekend coverage, holidays, and after-hours is required. ESSENTIAL DUTIES AND RESPONSIBILITIES: The main duties and responsibilities include the following, but are not limited to: Manages daily laboratory operations to ensure efficiency, accuracy, and compliance. Prepares schedules, coordinates workflow, and ensures adequate staffing coverage. Supervises laboratory personnel, including training, competency assessments, performance evaluations, and coaching. Ensures staff maintain required certifications, training, and ongoing competency, as applicable. Oversees workflow and prioritizes tasks to maintain turnaround time (TAT) and key performance indicator (KPI) goals. Monitors and ensures compliance with CAP, CLIA, corporate, and other regulatory bodies. Assists in developing and implementing standard operating procedures and training programs. Supports budgeting by providing input on supplies, staffing needs, and equipment requirements. Oversees inventory management to ensure appropriate stock levels and cost efficiency. Performs technical review of slides, stains, and methodologies; troubleshoots issues and document corrective actions. Promotes safety, compliance, and continuous process improvement across laboratory functions. Facilitates communication of new initiatives, policies, and workflows. Collaborates cross- functionally to maintain workflow, address operational issues, and support laboratory and operational goals. Performs other duties as assigned by the laboratory director. Who You Are: In-depth understanding of CLIA, CAP, and regulatory compliance standards. Demonstrated ability to lead and develop teams in a fast-paced, high-growth environment. Strong organizational, problem-solving, and communication skills. EDUCATION and/or EXPERIENCE Required: BA/BS degree; BS in chemical, physical, or biological science, or Cytotechnology preferred. Required: 5+ years of experience in a cytology or clinical laboratory; prior experience leading teams preferred. Required: ASCP certification; Preferred Cytologist, CT(ASCP) certification. OTHER SKILLS AND ATTRIBUTES Knowledge of laboratory regulations, protocols, and procedures. Critical thinking abilities. Ability to perform laboratory protocols and procedures. Ability to work in a team environment. Provides training and education for continuing education. Ability to make operational choices around how work gets done meeting quality and productivity standards, measurable goals for employees. Ability to evaluate and recommend changes to policies and establish procedures. Strong attention to detail and organization skills Basic computer skills, including data entry and use of LIMS Excellent written and oral communication skills Ability to work independently and exercise good judgement Demonstrated self-starter PHYSICAL REQUIREMENTS Repetitive movement of hands, arms, and legs Ability to stand or sit for extended periods of time Manual dexterity and visual acuity for handling and processing specimens Ability to wear personal protective equipment, including gloves, lab coats, and safety glasses Repetitive movement of fingers (typing and/or writing) Sitting, with occasional walking, standing, stooping, and moving about Occasionally required to lift to 25 pounds BSL2 laboratory environment &nbsp; #LI-Onsite &nbsp;The final salary offered to a successful candidate will be dependent on several factors that may include but are not limited to the type and length of experience within the job, type and length of experience within the industry, education, etc. Base pay is one part of the Total Package that is provided to compensate and recognize employees for their work, and this role may be eligible for additional discretionary bonuses/incentives, and restricted stock units. Veracyte is a multi-state employer, and this salary range may not reflect positions that work in other states.Pay range$108,000&mdash;$134,000 USD&nbsp; What We Can Offer You Veracyte is a growing company that offers significant career opportunities if you are curious, driven, patient-oriented and aspire to help us build a great company. We offer competitive compensation and benefits, and are committed to fostering an inclusive workforce, where diverse backgrounds are represented, engaged, and empowered to drive innovative ideas and decisions. We are thrilled to be recognized as a 2024 Certified™ Great Place to Work® in both the US and Israel - a testament to our dynamic, inclusive, and inspiring workplace where passion meets purpose. &nbsp; About Veracyte Veracyte&nbsp;(Nasdaq: VCYT) is a global genomic diagnostics company that improves patient care by providing answers to clinical questions, informing diagnosis and treatment decisions throughout the patient journey in cancer and other diseases. The company’s growing menu of genomic tests leverage advances in genomic science and technology, enabling patients to avoid risky, costly diagnostic procedures and quicken time to appropriate treatment. The company’s tests in lung cancer, prostate cancer, breast cancer, thyroid cancer, bladder cancer and idiopathic pulmonary fibrosis are available to patients and its lymphoma subtyping and renal cancer tests are in development. With Veracyte’s exclusive global license to a best-in-class diagnostics instrument platform, the company is positioned to deliver its tests to patients worldwide.&nbsp;Veracyte&nbsp;is based in&nbsp;South San Francisco, California. For more information, please visit&nbsp;www.veracyte.com and follow the company on X (Formerly Twitter). Veracyte, Inc. is an Equal Opportunity Employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status or disability status. Veracyte participates in E-Verify in the United States. View our&nbsp;CCPA Disclosure Notice. If you receive any suspicious alerts or communications through LinkedIn or other online job sites for any position at Veracyte, please exercise caution and promptly report any concerns to careers@veracyte.com

Manager, Cytology

At Veracyte, we offer exciting career opportunities for those interested in joining a pioneering team that is committed to transforming cancer care for patients across the globe. Working at Veracyte enables our employees to not only make a meaningful impact on the lives of patients, but to also learn and grow within a purpose driven&nbsp;environment. This is what we call the Veracyte way&nbsp;– it’s about how we work together, guided by our values, to give clinicians the insights they need to help patients make life-changing decisions.&nbsp; Our Values: We Seek A Better Way: We innovate boldly, learn from our setbacks, and are resilient in our pursuit to transform cancer care We Make It Happen: We act with urgency, commit to quality, and bring fun to our hard work We Are Stronger Together:&nbsp;We collaborate openly, seek to understand, and celebrate our wins We Care Deeply: We embrace our differences, do the right thing, and encourage each other &nbsp;The Position: &nbsp; Veracyte is seeking a Marketing Manager for the Prosigna Breast Cancer Assay, a genomic test designed to aid in treatment decisions for patients with breast cancer. The Marketing Manager will help drive global growth in Prosigna and breast cancer product portfolio by developing a multi-channel marketing plan, creating messaging, collateral and collaborating with field teams to enable sales growth. The ideal candidate will have experience with product marketing and brand development, gathering voice of customer feedback, product positioning, and digital marketing strategies. ESSENTIAL DUTIES AND RESPONSIBILITIES include the following. Other duties may be assigned. Execute marketing operations for all aspects of: Lead the development of the creation of global and US specific marketing materials Lead and support the development of content for digital marketing activities, including the website and social media, in collaboration with the corporate marketing team Lead conference planning and execution in collaboration with the corporate marketing team Budget management Closely partner with sales to: Develop and ensure that breast cancer messaging, sales tools, and other collateral are continuously relevant and accurate Create new marketing collateral and sales training, as needed Consistently keep a pulse on the latest market developments and proactively refine strategy, selling direction and tactics as necessary Distill customer feedback into actionable and appropriate marketing-related solutions Execute assigned aspects of the ongoing commercial initiatives to drive significant revenue growth Conduct qualitative and quantitative voice of customer research, market assessment, competitive analysis, as necessary to support product sales growth and product improvement Build relationships with key physicians to build domain expertise and strategic insights Who You Are: You are a highly motivated, results-driven individual with entrepreneurial drive and a track record of success in marketing. You have a deep sense of accountability and desire to own the product, from crafting the strategy to rolling up your sleeves and executing the tactics. Additional Qualifications Include: &nbsp; Bachelor’s degree in science required 5+ years combined experience in marketing/sales preferred Experience with LDT and IVD marketing Experience working cross-functionally Excellent attention to detail required Excellent presentation, written, verbal communication, and interpersonal skills Excellent analytical and technical skills Adaptability to changes and challenges Tenacity and the drive to make an impact Team player with demonstrated track record of collaboration with others Location: This role can be remote in the US. Minimum of 25% travel is expected. Travel to the San Diego, San Francisco and European home offices along with US and EU customer visits and conference attendance is expected #LI-Remote,&nbsp;#LI-Hybrid &nbsp;The final salary offered to a successful candidate will be dependent on several factors that may include but are not limited to the type and length of experience within the job, type and length of experience within the industry, education, etc. Base pay is one part of the Total Package that is provided to compensate and recognize employees for their work, and this role may be eligible for additional discretionary bonuses/incentives, and restricted stock units. Veracyte is a multi-state employer, and this salary range may not reflect positions that work in other states.Pay range$125,000&mdash;$148,000 USD&nbsp; What We Can Offer You Veracyte is a growing company that offers significant career opportunities if you are curious, driven, patient-oriented and aspire to help us build a great company. We offer competitive compensation and benefits, and are committed to fostering an inclusive workforce, where diverse backgrounds are represented, engaged, and empowered to drive innovative ideas and decisions. We are thrilled to be recognized as a 2024 Certified™ Great Place to Work® in both the US and Israel - a testament to our dynamic, inclusive, and inspiring workplace where passion meets purpose. &nbsp; About Veracyte Veracyte&nbsp;(Nasdaq: VCYT) is a global genomic diagnostics company that improves patient care by providing answers to clinical questions, informing diagnosis and treatment decisions throughout the patient journey in cancer and other diseases. The company’s growing menu of genomic tests leverage advances in genomic science and technology, enabling patients to avoid risky, costly diagnostic procedures and quicken time to appropriate treatment. The company’s tests in lung cancer, prostate cancer, breast cancer, thyroid cancer, bladder cancer and idiopathic pulmonary fibrosis are available to patients and its lymphoma subtyping and renal cancer tests are in development. With Veracyte’s exclusive global license to a best-in-class diagnostics instrument platform, the company is positioned to deliver its tests to patients worldwide.&nbsp;Veracyte&nbsp;is based in&nbsp;South San Francisco, California. For more information, please visit&nbsp;www.veracyte.com and follow the company on X (Formerly Twitter). Veracyte, Inc. is an Equal Opportunity Employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status or disability status. Veracyte participates in E-Verify in the United States. View our&nbsp;CCPA Disclosure Notice. If you receive any suspicious alerts or communications through LinkedIn or other online job sites for any position at Veracyte, please exercise caution and promptly report any concerns to careers@veracyte.com

Marketing Manager - Breast

At Veracyte, we offer exciting career opportunities for those interested in joining a pioneering team that is committed to transforming cancer care for patients across the globe. Working at Veracyte enables our employees to not only make a meaningful impact on the lives of patients, but to also learn and grow within a purpose driven&nbsp;environment. This is what we call the Veracyte way&nbsp;– it’s about how we work together, guided by our values, to give clinicians the insights they need to help patients make life-changing decisions.&nbsp; Our Values: We Seek A Better Way: We innovate boldly, learn from our setbacks, and are resilient in our pursuit to transform cancer care We Make It Happen: We act with urgency, commit to quality, and bring fun to our hard work We Are Stronger Together:&nbsp;We collaborate openly, seek to understand, and celebrate our wins We Care Deeply: We embrace our differences, do the right thing, and encourage each other &nbsp;The Position: The Marketing Specialist will support the Urology business unit by managing marketing processes, ensuring brand consistency, and assisting in the execution of key initiatives across campaigns, events, and sales enablement. This role works closely with marketing leadership, sales, and cross-functional partners to drive operational excellence and support Veracyte’s growth in the urology market.&nbsp; This is a hybrid position based in our San Diego, CA location.&nbsp; Essential Duties and Responsibilities: Marketing Collateral &amp; Brand Consistency: Manage the review, approval, digital storage, and distribution of all marketing materials; support updates to ensure alignment with brand guidelines (Adobe Creative Suite proficiency required).&nbsp; Content Coordination &amp; Management: Partner with marketing leadership to coordinate content across teams, ensure timely updates, and maintain consistency of collateral used internally and externally (experience strongly preferred).&nbsp; Marketing Operations: Support budget tracking and forecasting in collaboration with marketing leadership; process inbound leads from the marketing automation platform and ensure proper routing.&nbsp; Vendor &amp; Contract Management: Manage agreements with third-party vendors and partners, overseeing the internal approval process for contracts; generate purchase orders as needed for sponsorships, educational content, events, and other marketing activities.&nbsp; Conference &amp; Event Support: Assist with scheduling and logistics for conferences and tradeshows, including prospectus completion, purchase orders, material coordination, hotel blocking, and communication with attendees.&nbsp; Sales &amp; Marketing Support: Provide support for requests from the sales and marketing teams as needed, ensuring timely coordination and delivery of resources.&nbsp; Who You Are: Bachelor’s degree required 5 years of marketing experience strongly preferred, preferably in biotech, diagnostics, or healthcare.&nbsp; Proficiency in Adobe Creative Suite &nbsp; Experience in content coordination and collateral management&nbsp; Experience with content management systems is a plus.&nbsp; Strong organizational skills with the ability to manage multiple projects in a fast-paced environment.&nbsp; Excellent written and verbal communication skills, with a collaborative mindset.&nbsp; Adaptability, attention to detail, and drive to make an impact.&nbsp; #LI-Hybrid &nbsp;The final salary offered to a successful candidate will be dependent on several factors that may include but are not limited to the type and length of experience within the job, type and length of experience within the industry, education, etc. Base pay is one part of the Total Package that is provided to compensate and recognize employees for their work, and this role may be eligible for additional discretionary bonuses/incentives, and restricted stock units. Veracyte is a multi-state employer, and this salary range may not reflect positions that work in other states.Pay range$98,000&mdash;$112,000 USD&nbsp; What We Can Offer You Veracyte is a growing company that offers significant career opportunities if you are curious, driven, patient-oriented and aspire to help us build a great company. We offer competitive compensation and benefits, and are committed to fostering an inclusive workforce, where diverse backgrounds are represented, engaged, and empowered to drive innovative ideas and decisions. We are thrilled to be recognized as a 2024 Certified™ Great Place to Work® in both the US and Israel - a testament to our dynamic, inclusive, and inspiring workplace where passion meets purpose. &nbsp; About Veracyte Veracyte&nbsp;(Nasdaq: VCYT) is a global genomic diagnostics company that improves patient care by providing answers to clinical questions, informing diagnosis and treatment decisions throughout the patient journey in cancer and other diseases. The company’s growing menu of genomic tests leverage advances in genomic science and technology, enabling patients to avoid risky, costly diagnostic procedures and quicken time to appropriate treatment. The company’s tests in lung cancer, prostate cancer, breast cancer, thyroid cancer, bladder cancer and idiopathic pulmonary fibrosis are available to patients and its lymphoma subtyping and renal cancer tests are in development. With Veracyte’s exclusive global license to a best-in-class diagnostics instrument platform, the company is positioned to deliver its tests to patients worldwide.&nbsp;Veracyte&nbsp;is based in&nbsp;South San Francisco, California. For more information, please visit&nbsp;www.veracyte.com and follow the company on X (Formerly Twitter). Veracyte, Inc. is an Equal Opportunity Employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status or disability status. Veracyte participates in E-Verify in the United States. View our&nbsp;CCPA Disclosure Notice. If you receive any suspicious alerts or communications through LinkedIn or other online job sites for any position at Veracyte, please exercise caution and promptly report any concerns to careers@veracyte.com

Marketing Specialist

At Veracyte, we offer exciting career opportunities for those interested in joining a pioneering team that is committed to transforming cancer care for patients across the globe. Working at Veracyte enables our employees to not only make a meaningful impact on the lives of patients, but to also learn and grow within a purpose driven&nbsp;environment. This is what we call the Veracyte way&nbsp;– it’s about how we work together, guided by our values, to give clinicians the insights they need to help patients make life-changing decisions.&nbsp; Our Values: We Seek A Better Way: We innovate boldly, learn from our setbacks, and are resilient in our pursuit to transform cancer care We Make It Happen: We act with urgency, commit to quality, and bring fun to our hard work We Are Stronger Together:&nbsp;We collaborate openly, seek to understand, and celebrate our wins We Care Deeply: We embrace our differences, do the right thing, and encourage each other &nbsp;The Position: &nbsp;Our Medical Science Liaisons (MSLs) is a critical part of Decipher Urologic Cancers business group. &nbsp;They are clinical/genomic experts who provide clinical product education to our customers and our field teams with the goal of driving understanding and adoption of our novel diagnostics. Our MSLs have strong communication skills and are energized by building rapport with our HCP customers as well as our sales team and addressing their educational and customer needs. They will be expected to partner closely across the organization to serve as a scientific and clinical resource for the company's products and associated disease states, providing both internal and external educational support. This also includes providing support for the development of multi-channel medical educational activities and tools across the product lifecycle such as speaker programs, educational materials, slide creation, and on-line educational events. The MSL functions as a field-based member of the marketing department within the commercial team. This is a full-time position with approximately 70% of time devoted to client-facing activities mostly at the request of the sales team, in-person and remote, and 30% spent on internal collaborations and special projects. This role requires at least 60% travel and provides coverage of key customers and support of field teams over multiple states in the United States. The coverage geography will be spread amongst states in the Midwest and Northwest, with occasional trips to other parts of the country.&nbsp; We would prefer a candidate located in South San Francisco, but are also open to candidates located in San Diego, Denver, Dallas, Seattle, St. Louis and Kansas City.&nbsp; Who You Are: Advanced scientific or clinical degree required- PhD, MD, NP, PA, CGC At least 5 years of clinical experience – preferably urology/radiation oncology-focused prior experience as an MSL in the introduction of a novel clinical assay preferred Advanced understanding of tumor biology and molecular testing and/or related working experience critical for success in this role Outstanding interpersonal skills and a team player, demonstrating customer centricity, passion for patients and desire to help the cross-functional teams succeed Outstanding oral and written presentation skills, to convey complex study findings and data to audiences with varying degrees of scientific/clinical/healthcare knowledge Outstanding interpersonal skills in building rapport, probing, situational awareness and adapting communication and content based on real time needs of audience Willingness and ability to travel within defined region with proximity to a major airport A detail-oriented, organized, self-starter approach, with strong ability to multitask yet prioritize workload #LI-Onsite, #Ll-Remote, #LI-Hybrid &nbsp;The final salary offered to a successful candidate will be dependent on several factors that may include but are not limited to the type and length of experience within the job, type and length of experience within the industry, education, etc. Base pay is one part of the Total Package that is provided to compensate and recognize employees for their work, and this role may be eligible for additional discretionary bonuses/incentives, and restricted stock units. Veracyte is a multi-state employer, and this salary range may not reflect positions that work in other states.Pay range$165,000&mdash;$192,000 USD&nbsp; What We Can Offer You Veracyte is a growing company that offers significant career opportunities if you are curious, driven, patient-oriented and aspire to help us build a great company. We offer competitive compensation and benefits, and are committed to fostering an inclusive workforce, where diverse backgrounds are represented, engaged, and empowered to drive innovative ideas and decisions. We are thrilled to be recognized as a 2024 Certified™ Great Place to Work® in both the US and Israel - a testament to our dynamic, inclusive, and inspiring workplace where passion meets purpose. &nbsp; About Veracyte Veracyte&nbsp;(Nasdaq: VCYT) is a global genomic diagnostics company that improves patient care by providing answers to clinical questions, informing diagnosis and treatment decisions throughout the patient journey in cancer and other diseases. The company’s growing menu of genomic tests leverage advances in genomic science and technology, enabling patients to avoid risky, costly diagnostic procedures and quicken time to appropriate treatment. The company’s tests in lung cancer, prostate cancer, breast cancer, thyroid cancer, bladder cancer and idiopathic pulmonary fibrosis are available to patients and its lymphoma subtyping and renal cancer tests are in development. With Veracyte’s exclusive global license to a best-in-class diagnostics instrument platform, the company is positioned to deliver its tests to patients worldwide.&nbsp;Veracyte&nbsp;is based in&nbsp;South San Francisco, California. For more information, please visit&nbsp;www.veracyte.com and follow the company on X (Formerly Twitter). Veracyte, Inc. is an Equal Opportunity Employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status or disability status. Veracyte participates in E-Verify in the United States. View our&nbsp;CCPA Disclosure Notice. If you receive any suspicious alerts or communications through LinkedIn or other online job sites for any position at Veracyte, please exercise caution and promptly report any concerns to careers@veracyte.com

Medical Science Liaison

At Veracyte, we offer exciting career opportunities for those interested in joining a pioneering team that is committed to transforming cancer care for patients across the globe. Working at Veracyte enables our employees to not only make a meaningful impact on the lives of patients, but to also learn and grow within a purpose driven&nbsp;environment. This is what we call the Veracyte way&nbsp;– it’s about how we work together, guided by our values, to give clinicians the insights they need to help patients make life-changing decisions.&nbsp; Our Values: We Seek A Better Way: We innovate boldly, learn from our setbacks, and are resilient in our pursuit to transform cancer care We Make It Happen: We act with urgency, commit to quality, and bring fun to our hard work We Are Stronger Together:&nbsp;We collaborate openly, seek to understand, and celebrate our wins We Care Deeply: We embrace our differences, do the right thing, and encourage each other &nbsp;The Position: &nbsp; A Medical Science Liaison (MSL) at Veracyte is a genomic and disease state expert who provides clinical and product education to external Health Care Providers (HCP) to drive understanding and adoption of the company’s molecular test for breast cancer. They are recognized experts and trusted partners, serving as the primary scientific and clinical resource to external and internal stakeholders. MSLs support the development of multi-channel educational activities and tools throughout the product lifecycle, such as speaker programs, educational materials, conference coverage, and online educational events. An essential responsibility for this position will be to stimulate investigator-initiated studies utilizing Veracyte’s Prosigna Breast Cancer test and work closely with Key Opinion Leaders (KOLs) through study completion. The MSL is a field-based member of the medical affairs department, working closely with sales and marketing team members. This is a full-time position with approximately 80% of time devoted to HCPs-facing activities (in-person or virtually), partly at the request of the sales team and partly by proactively reaching out to KOLs. MSLs will spend 20% of their time on internal collaborations across marketing, sales, and medical affairs departments. This role requires at least 60% travel, providing education to key HCPs and support to field team members in the western United States. ESSENTIAL DUTIES AND RESPONSIBILITIES include the following. Other duties may be assigned. &nbsp; Proactively identify, develop, and maintain strong relationships with academic and community physicians by promoting understanding and adoption of Veracyte’s Prosigna Breast Cancer test. Identify KOLs, stimulate investigator-initiated studies, and support through study completion and article publication. Provide tailored presentations to external HCPs at the request of sales team members. Support the medical affairs team in collecting real-world evidence supporting the clinical utility of Veracyte’s tests. Create and implement strategies supporting product improvements in collaboration with medical affairs, research and development, managed care, and sales. Critically review the literature and build educational materials for external HCP and internal stakeholder consumption. Serve as a primary scientific and clinical resource to the marketing and sales team members providing medical updates, journal clubs, and MSL office hours. Assist the managed care team in setting up applications for insurance coverage by providing up-to-date scientific and clinical information supporting the clinical utility of Veracyte’s tests. Provide conference coverage supporting the sales team and prepare a post-conference summary of relevant talks to the leadership team &nbsp; Who You Are: MSLs are energized by providing clear solutions to physicians and patients for currently unmet diagnostic and clinical needs. They can assimilate and distill large amounts of complex scientific and clinical information into easy to digest format. Concise, clear, and compliant communication is a must. MSLs have a deep understanding of clinical research and the publication process and provide critical support to KOLs engaged in investigator-initiated studies. MSLs support the development of multi-channel educational activities and tools throughout the product lifecycle, such as speaker programs, educational materials, conference coverage, and online educational events. Additional Qualifications Include: &nbsp; Terminal scientific and/or clinical degree – Ph.D., M.D., Pharm.D., and D.O. At least 5 years of clinical or industry experience, preferably with an oncology focus. Deep understanding of the peer-review publication process. Advanced understanding of the genetic basis for disease and modern genomic techniques is critical for success in this role. Prior experience as an MSL in introducing and supporting novel diagnostic assays is desired. Overall solid written and verbal communication skills to convey complex study results to audiences with varying degrees of scientific/clinical knowledge. Outstanding interpersonal skills in understanding HCP needs and situational awareness to adapt content and communication style in real time. Team player working in synergy with marketing and sales team members providing accurate, comprehensive, and timely scientific and clinical support. Demonstrating customer-centricity and passion for helping patients. Familiarity with statistical methodologies. A detail-oriented, organized self-starter with a strong ability to prioritize workload. Location in proximity to airport hub and ability to travel within the defined region. &nbsp; &nbsp; #LI-Remote,&nbsp;#LI-Hybrid &nbsp;The final salary offered to a successful candidate will be dependent on several factors that may include but are not limited to the type and length of experience within the job, type and length of experience within the industry, education, etc. Base pay is one part of the Total Package that is provided to compensate and recognize employees for their work, and this role may be eligible for additional discretionary bonuses/incentives, and restricted stock units. Veracyte is a multi-state employer, and this salary range may not reflect positions that work in other states.Pay range$180,000&mdash;$192,000 USD&nbsp; What We Can Offer You Veracyte is a growing company that offers significant career opportunities if you are curious, driven, patient-oriented and aspire to help us build a great company. We offer competitive compensation and benefits, and are committed to fostering an inclusive workforce, where diverse backgrounds are represented, engaged, and empowered to drive innovative ideas and decisions. We are thrilled to be recognized as a 2024 Certified™ Great Place to Work® in both the US and Israel - a testament to our dynamic, inclusive, and inspiring workplace where passion meets purpose. &nbsp; About Veracyte Veracyte&nbsp;(Nasdaq: VCYT) is a global genomic diagnostics company that improves patient care by providing answers to clinical questions, informing diagnosis and treatment decisions throughout the patient journey in cancer and other diseases. The company’s growing menu of genomic tests leverage advances in genomic science and technology, enabling patients to avoid risky, costly diagnostic procedures and quicken time to appropriate treatment. The company’s tests in lung cancer, prostate cancer, breast cancer, thyroid cancer, bladder cancer and idiopathic pulmonary fibrosis are available to patients and its lymphoma subtyping and renal cancer tests are in development. With Veracyte’s exclusive global license to a best-in-class diagnostics instrument platform, the company is positioned to deliver its tests to patients worldwide.&nbsp;Veracyte&nbsp;is based in&nbsp;South San Francisco, California. For more information, please visit&nbsp;www.veracyte.com and follow the company on X (Formerly Twitter). Veracyte, Inc. is an Equal Opportunity Employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status or disability status. Veracyte participates in E-Verify in the United States. View our&nbsp;CCPA Disclosure Notice. If you receive any suspicious alerts or communications through LinkedIn or other online job sites for any position at Veracyte, please exercise caution and promptly report any concerns to careers@veracyte.com

Medical Science Liaison - Eastern US

At Veracyte, we offer exciting career opportunities for those interested in joining a pioneering team that is committed to transforming cancer care for patients across the globe. Working at Veracyte enables our employees to not only make a meaningful impact on the lives of patients, but to also learn and grow within a purpose driven&nbsp;environment. This is what we call the Veracyte way&nbsp;– it’s about how we work together, guided by our values, to give clinicians the insights they need to help patients make life-changing decisions.&nbsp; Our Values: We Seek A Better Way: We innovate boldly, learn from our setbacks, and are resilient in our pursuit to transform cancer care We Make It Happen: We act with urgency, commit to quality, and bring fun to our hard work We Are Stronger Together:&nbsp;We collaborate openly, seek to understand, and celebrate our wins We Care Deeply: We embrace our differences, do the right thing, and encourage each other &nbsp;The Position: A Medical Science Liaison (MSL) at Veracyte is a genomic and disease state expert who provides clinical and product education to external Health Care Providers (HCP) to drive understanding and adoption of the company’s molecular test for breast cancer. They are recognized experts and trusted partners, serving as the primary scientific and clinical resource to external and internal stakeholders. MSLs support the development of multi-channel educational activities and tools throughout the product lifecycle, such as speaker programs, educational materials, conference coverage, and online educational events. An essential responsibility for this position will be to stimulate investigator-initiated studies utilizing Veracyte’s Prosigna Breast Cancer test and work closely with Key Opinion Leaders (KOLs) through study completion. The MSL is a field-based member of the medical affairs department, working closely with sales and marketing team members. This is a full-time position with approximately 80% of time devoted to HCPs-facing activities (in-person or virtually), partly at the request of the sales team and partly by proactively reaching out to KOLs. MSLs will spend 20% of their time on internal collaborations across marketing, sales, and medical affairs departments. This role requires at least 60% travel, providing education to key HCPs and support to field team members in the western United States. ESSENTIAL DUTIES AND RESPONSIBILITIES include the following. Other duties may be assigned. Proactively identify, develop, and maintain strong relationships with academic and community physicians by promoting understanding and adoption of Veracyte’s Prosigna Breast Cancer test. Identify KOLs, stimulate investigator-initiated studies, and support through study completion and article publication. Provide tailored presentations to external HCPs at the request of sales team members. Support the medical affairs team in collecting real-world evidence supporting the clinical utility of Veracyte’s tests. Create and implement strategies supporting product improvements in collaboration with medical affairs, research and development, managed care, and sales. Critically review the literature and build educational materials for external HCP and internal stakeholder consumption. Serve as a primary scientific and clinical resource to the marketing and sales team members providing medical updates, journal clubs, and MSL office hours. Assist the managed care team in setting up applications for insurance coverage by providing up-to-date scientific and clinical information supporting the clinical utility of Veracyte’s tests. Provide conference coverage supporting the sales team and prepare a post-conference summary of relevant talks to the leadership team Who You Are: MSLs are energized by providing clear solutions to physicians and patients for currently unmet diagnostic and clinical needs. They can assimilate and distill large amounts of complex scientific and clinical information into easy to digest format. Concise, clear, and compliant communication is a must. MSLs have a deep understanding of clinical research and the publication process and provide critical support to KOLs engaged in investigator-initiated studies. MSLs support the development of multi-channel educational activities and tools throughout the product lifecycle, such as speaker programs, educational materials, conference coverage, and online educational events. Additional Qualifications Include: Terminal scientific and/or clinical degree – Ph.D., M.D., Pharm.D., and D.O. At least 5 years of clinical or industry experience, preferably with an oncology focus. Deep understanding of the peer-review publication process. Advanced understanding of the genetic basis for disease and modern genomic techniques is critical for success in this role. Prior experience as an MSL in introducing and supporting novel diagnostic assays is desired. Overall solid written and verbal communication skills to convey complex study results to audiences with varying degrees of scientific/clinical knowledge. Outstanding interpersonal skills in understanding HCP needs and situational awareness to adapt content and communication style in real time. Team player working in synergy with marketing and sales team members providing accurate, comprehensive, and timely scientific and clinical support. Demonstrating customer-centricity and passion for helping patients. Familiarity with statistical methodologies. A detail-oriented, organized self-starter with a strong ability to prioritize workload. Location in proximity to airport hub and ability to travel within the defined region. &nbsp; &nbsp; #LI-Remote,&nbsp;#LI-Hybrid &nbsp;The final salary offered to a successful candidate will be dependent on several factors that may include but are not limited to the type and length of experience within the job, type and length of experience within the industry, education, etc. Base pay is one part of the Total Package that is provided to compensate and recognize employees for their work, and this role may be eligible for additional discretionary bonuses/incentives, and restricted stock units. Veracyte is a multi-state employer, and this salary range may not reflect positions that work in other states.Pay range$180,000&mdash;$192,000 USD&nbsp; What We Can Offer You Veracyte is a growing company that offers significant career opportunities if you are curious, driven, patient-oriented and aspire to help us build a great company. We offer competitive compensation and benefits, and are committed to fostering an inclusive workforce, where diverse backgrounds are represented, engaged, and empowered to drive innovative ideas and decisions. We are thrilled to be recognized as a 2024 Certified™ Great Place to Work® in both the US and Israel - a testament to our dynamic, inclusive, and inspiring workplace where passion meets purpose. &nbsp; About Veracyte Veracyte&nbsp;(Nasdaq: VCYT) is a global genomic diagnostics company that improves patient care by providing answers to clinical questions, informing diagnosis and treatment decisions throughout the patient journey in cancer and other diseases. The company’s growing menu of genomic tests leverage advances in genomic science and technology, enabling patients to avoid risky, costly diagnostic procedures and quicken time to appropriate treatment. The company’s tests in lung cancer, prostate cancer, breast cancer, thyroid cancer, bladder cancer and idiopathic pulmonary fibrosis are available to patients and its lymphoma subtyping and renal cancer tests are in development. With Veracyte’s exclusive global license to a best-in-class diagnostics instrument platform, the company is positioned to deliver its tests to patients worldwide.&nbsp;Veracyte&nbsp;is based in&nbsp;South San Francisco, California. For more information, please visit&nbsp;www.veracyte.com and follow the company on X (Formerly Twitter). Veracyte, Inc. is an Equal Opportunity Employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status or disability status. Veracyte participates in E-Verify in the United States. View our&nbsp;CCPA Disclosure Notice. If you receive any suspicious alerts or communications through LinkedIn or other online job sites for any position at Veracyte, please exercise caution and promptly report any concerns to careers@veracyte.com

Medical Science Liaison - Western US

At Veracyte, we offer exciting career opportunities for those interested in joining a pioneering team that is committed to transforming cancer care for patients across the globe. Working at Veracyte enables our employees to not only make a meaningful impact on the lives of patients, but to also learn and grow within a purpose driven&nbsp;environment. This is what we call the Veracyte way&nbsp;– it’s about how we work together, guided by our values, to give clinicians the insights they need to help patients make life-changing decisions.&nbsp; Our Values: We Seek A Better Way: We innovate boldly, learn from our setbacks, and are resilient in our pursuit to transform cancer care We Make It Happen: We act with urgency, commit to quality, and bring fun to our hard work We Are Stronger Together:&nbsp;We collaborate openly, seek to understand, and celebrate our wins We Care Deeply: We embrace our differences, do the right thing, and encourage each other &nbsp;The Position: Location: This is a hybrid/onsite position based in our San Diego location.&nbsp; We are seeking a dynamic and strategic Product Manager to support the development and commercialization of Veracyte's bladder cancer portfolio. This role will be instrumental in helping bring these precision oncology tools to market by participating in core team meetings, driving product development deliverables, shaping commercial positioning, and ensuring alignment with customer needs, clinical utility, and market trends. The ideal candidate brings a blend of scientific acumen, market insight, and cross-functional execution skills.&nbsp; Key Responsibilities&nbsp; Product Development &amp; Core Team Involvement&nbsp; Serve as the product management representative on core teams. Collaborate with R&amp;D, Clinical, and Regulatory teams to define product requirements and support development milestones.&nbsp; Track and manage product development deliverables, timelines, and documentation to ensure cross-functional alignment.&nbsp; Help prepare for internal reviews and stage-gate deliverables.&nbsp; Market Research &amp; Competitive Intelligence&nbsp; Monitor the MRD and bladder cancer testing landscapes, including competitive product developments, clinical trials, and scientific publications.&nbsp; Conduct primary and secondary market research to better understand customer needs, value drivers, and market opportunities.&nbsp; Track competitive threats and synthesize insights to inform differentiation strategy and roadmap planning.&nbsp; Go-to-Market Strategy &amp; Commercial Support&nbsp; Support development of positioning, messaging, and value proposition for Veracyte's bladder product portfolio.&nbsp; Collaborate with medical affairs and marketing teams to provide input into content strategy, including sales training, promotional materials, and conference assets.&nbsp; Engage in voice of customer activities to gather insights that directly inform product strategy, positioning, and development priorities.&nbsp; Support commercial launch planning by contributing to launch timelines, cross-functional readiness activities, positioning strategy, and development of key materials.&nbsp; Portfolio Integration &amp; Strategic Input&nbsp; Develop a deep understanding of the Decipher Bladder portfolio and contribute to roadmap planning across products and indications.&nbsp; Identify potential synergies between MRD and subtyping products to build a unified Decipher Bladder story.&nbsp; Provide insights to support business development, publication planning, and evidence generation strategy.&nbsp; &nbsp; Who You Are: Science educational background with marketing experience is required&nbsp; B.S. with at least 5 years of industry marketing experience OR master's in science, with at least 3 years of industry marketing experience&nbsp; Background in oncology, genomics, or urology-related diagnostics strongly preferred.&nbsp; Familiarity with MRD, molecular diagnostics, and the oncology clinical development environment a strong plus.&nbsp; Strong project management skills with ability to work across functions in a fast-paced, collaborative setting.&nbsp; Excellent written and verbal communication skills, with ability to translate complex scientific information for different audiences.&nbsp; Travel&nbsp; Up to 15%, including attendance at internal team meetings, scientific conferences, and customer events.&nbsp; &nbsp; &nbsp; #LI-Onsite, #LI-Hybrid &nbsp;The final salary offered to a successful candidate will be dependent on several factors that may include but are not limited to the type and length of experience within the job, type and length of experience within the industry, education, etc. Base pay is one part of the Total Package that is provided to compensate and recognize employees for their work, and this role may be eligible for additional discretionary bonuses/incentives, and restricted stock units. Veracyte is a multi-state employer, and this salary range may not reflect positions that work in other states.Pay range$118,000&mdash;$141,000 USD&nbsp; What We Can Offer You Veracyte is a growing company that offers significant career opportunities if you are curious, driven, patient-oriented and aspire to help us build a great company. We offer competitive compensation and benefits, and are committed to fostering an inclusive workforce, where diverse backgrounds are represented, engaged, and empowered to drive innovative ideas and decisions. We are thrilled to be recognized as a 2024 Certified™ Great Place to Work® in both the US and Israel - a testament to our dynamic, inclusive, and inspiring workplace where passion meets purpose. &nbsp; About Veracyte Veracyte&nbsp;(Nasdaq: VCYT) is a global genomic diagnostics company that improves patient care by providing answers to clinical questions, informing diagnosis and treatment decisions throughout the patient journey in cancer and other diseases. The company’s growing menu of genomic tests leverage advances in genomic science and technology, enabling patients to avoid risky, costly diagnostic procedures and quicken time to appropriate treatment. The company’s tests in lung cancer, prostate cancer, breast cancer, thyroid cancer, bladder cancer and idiopathic pulmonary fibrosis are available to patients and its lymphoma subtyping and renal cancer tests are in development. With Veracyte’s exclusive global license to a best-in-class diagnostics instrument platform, the company is positioned to deliver its tests to patients worldwide.&nbsp;Veracyte&nbsp;is based in&nbsp;South San Francisco, California. For more information, please visit&nbsp;www.veracyte.com and follow the company on X (Formerly Twitter). Veracyte, Inc. is an Equal Opportunity Employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status or disability status. Veracyte participates in E-Verify in the United States. View our&nbsp;CCPA Disclosure Notice. If you receive any suspicious alerts or communications through LinkedIn or other online job sites for any position at Veracyte, please exercise caution and promptly report any concerns to careers@veracyte.com

Product Manager

At Veracyte, we offer exciting career opportunities for those interested in joining a pioneering team that is committed to transforming cancer care for patients across the globe. Working at Veracyte enables our employees to not only make a meaningful impact on the lives of patients, but to also learn and grow within a purpose driven&nbsp;environment. This is what we call the Veracyte way&nbsp;– it’s about how we work together, guided by our values, to give clinicians the insights they need to help patients make life-changing decisions.&nbsp; Our Values: We Seek A Better Way: We innovate boldly, learn from our setbacks, and are resilient in our pursuit to transform cancer care We Make It Happen: We act with urgency, commit to quality, and bring fun to our hard work We Are Stronger Together:&nbsp;We collaborate openly, seek to understand, and celebrate our wins We Care Deeply: We embrace our differences, do the right thing, and encourage each other &nbsp;The Position: The Project Manager will lead cross-functional teams in the development and commercialization of diagnostic products. This individual will be accountable for the successful delivery of complex projects to ensure business objectives are met and accomplished on time, within budget, and meet operational standards. The ideal candidate brings a deep understanding of product development under ISO13485, global regulatory pathways (e.g., EU IVDR, US FDA, etc.), and lifecycle management, along with strong leadership and communication skills to influence and guide teams in a fast-paced, regulated environment. Key Responsibilities: Lead project management of diagnostic development programs, from feasibility through development, verification/validation, regulatory submission, and commercialization. Drive cross-functional core teams (e.g., R&amp;D, QA/RA, Clinical Affairs, Manufacturing, Supply Chain, Commercial) to achieve program milestones on time, within scope, and on budget. Serve as a leader for assigned programs/projects with a high level of comfort in leading others including senior level personnel. Develop and maintain integrated project plans, timelines, risk registers, and mitigation strategies in alignment with the Product Development Process (PDP). Partner closely with regulatory and quality teams to align project activities with global regulatory pathways and regulations (e.g., IVDR, US FDA 510k, PMA, etc.) and quality management system requirements (e.g., ISO 13485, MDSAP, US FDA 21 CFR 820). Drive the team for the creation, review, and approvals of QMS documentation to support stage gate exists Prepare and present project status, risks, and strategic recommendations to governance committees and executive leadership. Foster a culture of accountability, collaboration, and continuous improvement across teams and stakeholders. Contribute to the development of PMO processes and tools. Identify, raise, and address issues or risks that arise as needed. Identify individual project resource requirements and portfolio capacity needed. Work with functional leads to identify and assign individual project responsibilities. Report regularly on project status, milestones, and KPIs to senior leadership. Contribute to the design and implementation of project management framework and tools. Foster a culture of continuous improvement and innovation within the project management team and broader organization. Work with business leaders and PMO leadership to align product / program roadmaps to goals, portfolio priorities, budgets, and resource plans. Other duties as assigned. Who You Are: Minimum of 5+ years of project management experience within the IVD, diagnostics, or medical device industry. Bachelor’s or master’s degree in life sciences, biotechnology, engineering, business, or related field preferred. Strong working knowledge of IVD design development processes, including clinical validation, regulatory pathways (e.g., CE/IVDR, ISO 13485, 510(k), PMA), and quality systems. Proficiency in project management methodologies and tools. Smartsheet knowledge and experience is preferred. Excellent communication, collaboration, and leadership skills with the ability to influence at all levels of the organization Ability to effectively lead people and drive results through cross-functional engagement/alignment. Experience working with cross-functional teams, including Product Development, clinical, regulatory, operations, and commercial departments. PMP or equivalent certification preferred. You are comfortable with ambiguity &nbsp; LI-Remote &nbsp;The final salary offered to a successful candidate will be dependent on several factors that may include but are not limited to the type and length of experience within the job, type and length of experience within the industry, education, etc. Base pay is one part of the Total Package that is provided to compensate and recognize employees for their work, and this role may be eligible for additional discretionary bonuses/incentives, and restricted stock units. Veracyte is a multi-state employer, and this salary range may not reflect positions that work in other states.Pay range$103,000&mdash;$118,000 USD&nbsp; What We Can Offer You Veracyte is a growing company that offers significant career opportunities if you are curious, driven, patient-oriented and aspire to help us build a great company. We offer competitive compensation and benefits, and are committed to fostering an inclusive workforce, where diverse backgrounds are represented, engaged, and empowered to drive innovative ideas and decisions. We are thrilled to be recognized as a 2024 Certified™ Great Place to Work® in both the US and Israel - a testament to our dynamic, inclusive, and inspiring workplace where passion meets purpose. &nbsp; About Veracyte Veracyte&nbsp;(Nasdaq: VCYT) is a global genomic diagnostics company that improves patient care by providing answers to clinical questions, informing diagnosis and treatment decisions throughout the patient journey in cancer and other diseases. The company’s growing menu of genomic tests leverage advances in genomic science and technology, enabling patients to avoid risky, costly diagnostic procedures and quicken time to appropriate treatment. The company’s tests in lung cancer, prostate cancer, breast cancer, thyroid cancer, bladder cancer and idiopathic pulmonary fibrosis are available to patients and its lymphoma subtyping and renal cancer tests are in development. With Veracyte’s exclusive global license to a best-in-class diagnostics instrument platform, the company is positioned to deliver its tests to patients worldwide.&nbsp;Veracyte&nbsp;is based in&nbsp;South San Francisco, California. For more information, please visit&nbsp;www.veracyte.com and follow the company on X (Formerly Twitter). Veracyte, Inc. is an Equal Opportunity Employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status or disability status. Veracyte participates in E-Verify in the United States. View our&nbsp;CCPA Disclosure Notice. If you receive any suspicious alerts or communications through LinkedIn or other online job sites for any position at Veracyte, please exercise caution and promptly report any concerns to careers@veracyte.com

Project Manager

At Veracyte, we offer exciting career opportunities for those interested in joining a pioneering team that is committed to transforming cancer care for patients across the globe. Working at Veracyte enables our employees to not only make a meaningful impact on the lives of patients, but to also learn and grow within a purpose driven&nbsp;environment. This is what we call the Veracyte way&nbsp;– it’s about how we work together, guided by our values, to give clinicians the insights they need to help patients make life-changing decisions.&nbsp; Our Values: We Seek A Better Way: We innovate boldly, learn from our setbacks, and are resilient in our pursuit to transform cancer care We Make It Happen: We act with urgency, commit to quality, and bring fun to our hard work We Are Stronger Together:&nbsp;We collaborate openly, seek to understand, and celebrate our wins We Care Deeply: We embrace our differences, do the right thing, and encourage each other &nbsp;The Position: We are seeking a self-driven and experienced Regulatory Affairs Manager with a strong background in the EU IVDR, including preparation of technical file submissions and all aspects of labeling. Experience in vigilance and post-market surveillance of in vitro diagnostics (IVD) would be advantageous. This role will play a key part in supporting the global expansion and lifecycle management of our IVD product portfolio which includes assay, software, and instrument components. The position will also contribute to the development of strategic regulatory processes and cross-functional initiatives aligned with international standards and regulations.The ideal candidate thrives in a fast-paced, collaborative, and technically complex environment and is committed to ensuring compliance throughout the product lifecycle – from development through post-market.You will report to the Senior Director of Global Regulatory Affairs (EU-based) and collaborate closely with the global Regulatory Affairs (RA) and Quality teams to ensure regulatory compliance, support product registrations globally, and contribute to vigilance and surveillance programs.Key Responsibilities: Take a lead role in ensuring regulatory compliance of IVDR regulatory submissions, labeling, including instructions for use, labels and safety data sheets. Support IVD product development teams by providing regulatory guidance on requirements, impacting new product introductions and changes to existing products. Help drive post-market surveillance (PMS) and vigilance reporting activities, including adverse event tracking, complaint trending, and periodic safety update reports (PSURs), in compliance with EU IVDR and other applicable regulations. Collaborate in the preparation, review, and submission of technical documentation to meet IVDR, MDSAP, and other global regulatory requirements. Participate in and support internal and external audits, inspections, and regulatory authority interactions related to PMS and vigilance activities. Assist in the development and implementation of regulatory policies and procedures to ensure effective global compliance and continuous improvement within the RA function. Represent Regulatory Affairs in cross-functional initiatives focused on product lifecycle management, regulatory readiness, and global market access strategies. Support internal and external training initiatives to increase organizational awareness of global labeling, post-market and vigilance requirements. Who You Are: Bachelor’s or Master’s degree in Life Sciences, Engineering, or a related field. Minimum of 5 years of IVD development for the EU market, labeling and regulatory affairs experience in the IVD medical device industry, with strong exposure to international regulatory submission documentation and post-market activities. Solid understanding of IVDR, ISO 13485, MDSAP, and other global regulatory frameworks. Ideally, proven experience of managing labeling, &nbsp;vigilance and PMS programs Excellent communication, analytical, and project management skills. Self-motivated, adaptable, and capable of working independently in a remote, globally distributed team. #LI-Remote &nbsp;&nbsp; What We Can Offer You Veracyte is a growing company that offers significant career opportunities if you are curious, driven, patient-oriented and aspire to help us build a great company. We offer competitive compensation and benefits, and are committed to fostering an inclusive workforce, where diverse backgrounds are represented, engaged, and empowered to drive innovative ideas and decisions. We are thrilled to be recognized as a 2024 Certified™ Great Place to Work® in both the US and Israel - a testament to our dynamic, inclusive, and inspiring workplace where passion meets purpose. &nbsp; About Veracyte Veracyte&nbsp;(Nasdaq: VCYT) is a global genomic diagnostics company that improves patient care by providing answers to clinical questions, informing diagnosis and treatment decisions throughout the patient journey in cancer and other diseases. The company’s growing menu of genomic tests leverage advances in genomic science and technology, enabling patients to avoid risky, costly diagnostic procedures and quicken time to appropriate treatment. The company’s tests in lung cancer, prostate cancer, breast cancer, thyroid cancer, bladder cancer and idiopathic pulmonary fibrosis are available to patients and its lymphoma subtyping and renal cancer tests are in development. With Veracyte’s exclusive global license to a best-in-class diagnostics instrument platform, the company is positioned to deliver its tests to patients worldwide.&nbsp;Veracyte&nbsp;is based in&nbsp;South San Francisco, California. For more information, please visit&nbsp;www.veracyte.com and follow the company on X (Formerly Twitter). Veracyte, Inc. is an Equal Opportunity Employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status or disability status. Veracyte participates in E-Verify in the United States. View our&nbsp;CCPA Disclosure Notice. If you receive any suspicious alerts or communications through LinkedIn or other online job sites for any position at Veracyte, please exercise caution and promptly report any concerns to careers@veracyte.com

Regulatory Affairs Manager, IVD

At Veracyte, we offer exciting career opportunities for those interested in joining a pioneering team that is committed to transforming cancer care for patients across the globe. Working at Veracyte enables our employees to not only make a meaningful impact on the lives of patients, but to also learn and grow within a purpose driven&nbsp;environment. This is what we call the Veracyte way&nbsp;– it’s about how we work together, guided by our values, to give clinicians the insights they need to help patients make life-changing decisions.&nbsp; Our Values: We Seek A Better Way: We innovate boldly, learn from our setbacks, and are resilient in our pursuit to transform cancer care We Make It Happen: We act with urgency, commit to quality, and bring fun to our hard work We Are Stronger Together:&nbsp;We collaborate openly, seek to understand, and celebrate our wins We Care Deeply: We embrace our differences, do the right thing, and encourage each other &nbsp;The Position: We are seeking a hands-on Senior CloudOps Engineer to execute our cloud operations strategy. In this critical role, you will lead the technical implementation for our AWS CloudOps strategy, driving the adoption of modern operational practices across the organization. You will be responsible for architecting and implementing highly automated, reliable, and cost-efficient systems that support our production services, R&amp;D initiatives, and corporate functions. The ideal candidate is a seasoned engineer with a deep passion for automation, a strategic mindset for system design, and proven experience mentoring and leading technical projects. This position is a hybrid role based out of our San Diego or South San Francisco office. We may also be open to remote for the ideal candidate.&nbsp; Responsibilities: Technical Leadership: Work with CloudOps leadership to craft the roadmap for cloud operations, setting technical standards and best practices. Mentor and guide other engineers on the team, fostering a culture of operational excellence and continuous improvement. Infrastructure as Code (IaC): Lead the design and implementation of key CloudOps requirements and initiatives. Develop solutions using imperative interfaces such as the AWS Cloud Development Kit (CDK) or Pulumi. Continuous Delivery (CD): Architect, build, and maintain robust CI/CD pipelines to automate application and infrastructure deployments, ensuring fast, safe, and reliable releases. Automation &amp; Scalability: Drive automation initiatives across the organization, developing scripts (Python, Bash, etc.) and tooling to eliminate manual tasks, improve system scalability, and streamline operational workflows. Reliability &amp; Observability: Implement and manage sophisticated monitoring, logging, and observability platforms (e.g., Amazon CloudWatch, Sumo Logic, Prometheus, Grafana) and lead the strategy for incident response and post-mortems. Cloud Financial Management (FinOps): Champion our cloud cost optimization efforts. You will lead the analysis of AWS spend, implement governance policies, and engineer solutions to maximize cost-efficiency without compromising performance. &nbsp; Who You Are: 8+ years of experience in CloudOps, SRE, or DevOps, with a proven history of technical leadership and project ownership. Expertise in Infrastructure as Code (AWS CDK, Pulumi, TF CDK) and designing complex CI/CD pipelines (AWS CodePipeline, GitLab CI, Jenkins). Expert-level Python scripting skills and deep knowledge of managing large-scale AWS Organizations using services like Control Tower, IAM Identity Center, VPC, and EC2. Experience with regulatory compliance frameworks, particularly in healthcare (HIPAA, CLIA, FDA). Strong skills in observability, FinOps (cloud cost optimization), cloud networking, and security. &nbsp; &nbsp; #LI-Hybrid &nbsp;The final salary offered to a successful candidate will be dependent on several factors that may include but are not limited to the type and length of experience within the job, type and length of experience within the industry, education, etc. Base pay is one part of the Total Package that is provided to compensate and recognize employees for their work, and this role may be eligible for additional discretionary bonuses/incentives, and restricted stock units. Veracyte is a multi-state employer, and this salary range may not reflect positions that work in other states.Pay range$155,000&mdash;$182,000 USD&nbsp; What We Can Offer You Veracyte is a growing company that offers significant career opportunities if you are curious, driven, patient-oriented and aspire to help us build a great company. We offer competitive compensation and benefits, and are committed to fostering an inclusive workforce, where diverse backgrounds are represented, engaged, and empowered to drive innovative ideas and decisions. We are thrilled to be recognized as a 2024 Certified™ Great Place to Work® in both the US and Israel - a testament to our dynamic, inclusive, and inspiring workplace where passion meets purpose. &nbsp; About Veracyte Veracyte&nbsp;(Nasdaq: VCYT) is a global genomic diagnostics company that improves patient care by providing answers to clinical questions, informing diagnosis and treatment decisions throughout the patient journey in cancer and other diseases. The company’s growing menu of genomic tests leverage advances in genomic science and technology, enabling patients to avoid risky, costly diagnostic procedures and quicken time to appropriate treatment. The company’s tests in lung cancer, prostate cancer, breast cancer, thyroid cancer, bladder cancer and idiopathic pulmonary fibrosis are available to patients and its lymphoma subtyping and renal cancer tests are in development. With Veracyte’s exclusive global license to a best-in-class diagnostics instrument platform, the company is positioned to deliver its tests to patients worldwide.&nbsp;Veracyte&nbsp;is based in&nbsp;South San Francisco, California. For more information, please visit&nbsp;www.veracyte.com and follow the company on X (Formerly Twitter). Veracyte, Inc. is an Equal Opportunity Employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status or disability status. Veracyte participates in E-Verify in the United States. View our&nbsp;CCPA Disclosure Notice. If you receive any suspicious alerts or communications through LinkedIn or other online job sites for any position at Veracyte, please exercise caution and promptly report any concerns to careers@veracyte.com

Senior CloudOps Engineer

At Veracyte, we offer exciting career opportunities for those interested in joining a pioneering team that is committed to transforming cancer care for patients across the globe. Working at Veracyte enables our employees to not only make a meaningful impact on the lives of patients, but to also learn and grow within a purpose driven&nbsp;environment. This is what we call the Veracyte way&nbsp;– it’s about how we work together, guided by our values, to give clinicians the insights they need to help patients make life-changing decisions.&nbsp; Our Values: We Seek A Better Way: We innovate boldly, learn from our setbacks, and are resilient in our pursuit to transform cancer care We Make It Happen: We act with urgency, commit to quality, and bring fun to our hard work We Are Stronger Together:&nbsp;We collaborate openly, seek to understand, and celebrate our wins We Care Deeply: We embrace our differences, do the right thing, and encourage each other &nbsp;The Position: The Senior Data Engineer will contribute to Veracyte’s success by designing, developing, and maintaining scalable cloud data infrastructure and pipelines to support the company’s data engineering needs. This role involves hands-on work with data lakes, meshes, and catalogs, collaborating with cross-functional teams in a Scrum environment to deliver high-quality data solutions. The Senior Data Engineer will support the implementation of data management frameworks and align with Veracyte’s global data strategy, policies, and digital transformation initiatives, including the Veracyte Lakehouse built on AWS and Snowflake. The position is based out of our San Diego office (hybrid) and we are also open to US Remote (working PST hours). Key Responsibilities: Design and Develop Data Infrastructure: Build and maintain scalable, efficient data pipelines and infrastructure for Lakehouse systems, including bronze, silver, and gold data layers. Work with technologies such as Amazon S3, Snowflake, AWS Glue, Lake Formation, and SageMaker for data storage, processing, and analytics. Collaborate Across Teams: Partner with the Technical Program Manager (TPM), data scientists, and stakeholders to understand business requirements and translate them into technical data solutions. Participate in Scrum processes, including backlog grooming, sprint planning, and handling data set requests via Jira. Optimize and Secure Data: Optimize data retrieval, processing, and ELT workflows for improved performance and reliability. Implement data security measures, governance policies, and compliance with PHI, consent, and regulatory requirements. Support Data Management Initiatives: Assist in identifying and assessing internal and external data sources for the data catalog. Contribute to the evaluation, development, or integration of user-friendly data catalog applications aligned with best practices. Help provide training and support to users of the data catalog. Contribute to Data Strategy: Provide technical input to support the development and implementation of Veracyte’s data strategy and policies. Collaborate on defining user stories, data quality levels (e.g., Medallion architecture), and access controls for datasets. Support data acquisition, curation, and delivery for use cases like AI model training, clinical decision support, and operational efficiency. Mentorship and Knowledge Sharing: Mentor junior data engineers and foster a culture of continuous learning. Share expertise in data engineering best practices, emerging technologies, and tools like Apache Parquet, Iceberg, and Zero-ETL integrations. Who You Are: Education: Bachelor’s or Master’s degree in Engineering, Computer Science, or a related field. Experience: 6+ years of experience (BS) or 3+ years (MS) in data engineering or a similar role. Hands-on experience with designing and deploying data pipelines in cloud environments, preferably AWS and/or GCP. Technical Skills: Proficiency in programming languages such as Python, Java, or Scala. Experience with AWS services (S3, Glue, Lake Formation, SageMaker) and Snowflake for data warehousing, ELT processes, and data modeling. Familiarity with data cataloging tools, data lakes, and governance best practices. Knowledge of open formats like Apache Parquet and Iceberg is a plus. Soft Skills: Strong problem-solving and analytical skills. Excellent communication and collaboration abilities to work effectively in a cross-functional Scrum team. Ability to thrive in a fast-paced, dynamic environment focused on data as a service (DaaS). &nbsp; &nbsp; #LI-Hybrid, or #LI-Remote &nbsp;The final salary offered to a successful candidate will be dependent on several factors that may include but are not limited to the type and length of experience within the job, type and length of experience within the industry, education, etc. Base pay is one part of the Total Package that is provided to compensate and recognize employees for their work, and this role may be eligible for additional discretionary bonuses/incentives, and restricted stock units. Veracyte is a multi-state employer, and this salary range may not reflect positions that work in other states.Pay range$155,000&mdash;$170,000 USD&nbsp; What We Can Offer You Veracyte is a growing company that offers significant career opportunities if you are curious, driven, patient-oriented and aspire to help us build a great company. We offer competitive compensation and benefits, and are committed to fostering an inclusive workforce, where diverse backgrounds are represented, engaged, and empowered to drive innovative ideas and decisions. We are thrilled to be recognized as a 2024 Certified™ Great Place to Work® in both the US and Israel - a testament to our dynamic, inclusive, and inspiring workplace where passion meets purpose. &nbsp; About Veracyte Veracyte&nbsp;(Nasdaq: VCYT) is a global genomic diagnostics company that improves patient care by providing answers to clinical questions, informing diagnosis and treatment decisions throughout the patient journey in cancer and other diseases. The company’s growing menu of genomic tests leverage advances in genomic science and technology, enabling patients to avoid risky, costly diagnostic procedures and quicken time to appropriate treatment. The company’s tests in lung cancer, prostate cancer, breast cancer, thyroid cancer, bladder cancer and idiopathic pulmonary fibrosis are available to patients and its lymphoma subtyping and renal cancer tests are in development. With Veracyte’s exclusive global license to a best-in-class diagnostics instrument platform, the company is positioned to deliver its tests to patients worldwide.&nbsp;Veracyte&nbsp;is based in&nbsp;South San Francisco, California. For more information, please visit&nbsp;www.veracyte.com and follow the company on X (Formerly Twitter). Veracyte, Inc. is an Equal Opportunity Employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status or disability status. Veracyte participates in E-Verify in the United States. View our&nbsp;CCPA Disclosure Notice. If you receive any suspicious alerts or communications through LinkedIn or other online job sites for any position at Veracyte, please exercise caution and promptly report any concerns to careers@veracyte.com

Senior Data Engineer

At Veracyte, we offer exciting career opportunities for those interested in joining a pioneering team that is committed to transforming cancer care for patients across the globe. Working at Veracyte enables our employees to not only make a meaningful impact on the lives of patients, but to also learn and grow within a purpose driven&nbsp;environment. This is what we call the Veracyte way&nbsp;– it’s about how we work together, guided by our values, to give clinicians the insights they need to help patients make life-changing decisions.&nbsp; Our Values: We Seek A Better Way: We innovate boldly, learn from our setbacks, and are resilient in our pursuit to transform cancer care We Make It Happen: We act with urgency, commit to quality, and bring fun to our hard work We Are Stronger Together:&nbsp;We collaborate openly, seek to understand, and celebrate our wins We Care Deeply: We embrace our differences, do the right thing, and encourage each other &nbsp;The Position: We are seeking a highly skilled and motivated LIMS Engineer to lead the architecture and design of cutting-edge Laboratory Information Management Systems (LIMS) and their integrations within a complex, fast-paced environment. The LIMS Engineer will collaborate closely with the LIMS Administrator, Lab Operations teams, and cross-functional technology teams to ensure that the platform is scalable, efficient, and aligned with both scientific and business objectives. This role requires hands-on experience with modern LIMS platforms such as L7 Informatics, Labbit, or other industry-leading solutions, and will be responsible for building robust system integrations using technologies like AWS, Mulesoft, and APIs. Strong programming skills in Python, SQL, PowerShell, and related tools will be essential for platform customization, automation, and data workflows in compliance-driven environments. This is a hybrid role based out of our San Diego office.&nbsp; Key Responsibilities: Lead or support full life-cycle LIMS implementations, including requirement gathering, system design, configuration, testing, deployment, and documentation. Design and develop scalable and maintainable LIMS architectures tailored to laboratory workflows and compliance requirements. Customize and extend LIMS platforms using scripting and automation tools to improve usability and performance. Collaborate with cross-functional teams including IT, lab personnel, and third-party vendors to ensure seamless system operation and user satisfaction. Develop and maintain integrations between LIMS and other enterprise platforms using APIs, Mulesoft, AWS services, and other middleware tools. Write and maintain scripts and tools using Python, SQL, PowerShell, and other languages to support system operations, data migrations, and automated workflows. Support data structure development and integration efforts, especially using JSON and/or GraphDB Ensure LIMS systems are compliant with regulatory standards such as GxP, CAP/CLIA, and other relevant quality frameworks. Provide ongoing support, troubleshooting, performance tuning, and end-user training for LIMS systems Who You Are: Bachelor’s or Master’s degree in Computer Science, Bioinformatics, Engineering, or a related technical field. 5-7+ years of experience in LIMS engineering, implementation, and support. Hands-on experience with one or more modern LIMS platforms (e.g., L7 Informatics, Labbit, Thermo Fisher SampleManager, LabWare, etc.). Proficiency in JSON, Python, SQL, PowerShell, and scripting for automation and data processing. Strong understanding of LIMS architecture, relational databases, and lab workflows. Proven experience in platform integrations using AWS services, Mulesoft, and REST/SOAP APIs. Solid grasp of data security, integrity, and compliance in regulated environments. Excellent problem-solving, communication, and documentation skills. Preferred Qualifications: Experience with Agile development methodologies and DevOps practices. Familiarity with CI/CD pipelines and infrastructure-as-code (e.g., Terraform, CloudFormation). Knowledge of laboratory instruments and ELNs (Electronic Lab Notebooks) integration. Certification in AWS, Mulesoft, or relevant LIMS platforms. &nbsp; #LI-Hybrid &nbsp;The final salary offered to a successful candidate will be dependent on several factors that may include but are not limited to the type and length of experience within the job, type and length of experience within the industry, education, etc. Base pay is one part of the Total Package that is provided to compensate and recognize employees for their work, and this role may be eligible for additional discretionary bonuses/incentives, and restricted stock units. Veracyte is a multi-state employer, and this salary range may not reflect positions that work in other states.Pay range$143,000&mdash;$157,000 USD&nbsp; What We Can Offer You Veracyte is a growing company that offers significant career opportunities if you are curious, driven, patient-oriented and aspire to help us build a great company. We offer competitive compensation and benefits, and are committed to fostering an inclusive workforce, where diverse backgrounds are represented, engaged, and empowered to drive innovative ideas and decisions. We are thrilled to be recognized as a 2024 Certified™ Great Place to Work® in both the US and Israel - a testament to our dynamic, inclusive, and inspiring workplace where passion meets purpose. &nbsp; About Veracyte Veracyte&nbsp;(Nasdaq: VCYT) is a global genomic diagnostics company that improves patient care by providing answers to clinical questions, informing diagnosis and treatment decisions throughout the patient journey in cancer and other diseases. The company’s growing menu of genomic tests leverage advances in genomic science and technology, enabling patients to avoid risky, costly diagnostic procedures and quicken time to appropriate treatment. The company’s tests in lung cancer, prostate cancer, breast cancer, thyroid cancer, bladder cancer and idiopathic pulmonary fibrosis are available to patients and its lymphoma subtyping and renal cancer tests are in development. With Veracyte’s exclusive global license to a best-in-class diagnostics instrument platform, the company is positioned to deliver its tests to patients worldwide.&nbsp;Veracyte&nbsp;is based in&nbsp;South San Francisco, California. For more information, please visit&nbsp;www.veracyte.com and follow the company on X (Formerly Twitter). Veracyte, Inc. is an Equal Opportunity Employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status or disability status. Veracyte participates in E-Verify in the United States. View our&nbsp;CCPA Disclosure Notice. If you receive any suspicious alerts or communications through LinkedIn or other online job sites for any position at Veracyte, please exercise caution and promptly report any concerns to careers@veracyte.com

Senior LIMS Engineer

At Veracyte, we offer exciting career opportunities for those interested in joining a pioneering team that is committed to transforming cancer care for patients across the globe. Working at Veracyte enables our employees to not only make a meaningful impact on the lives of patients, but to also learn and grow within a purpose driven&nbsp;environment. This is what we call the Veracyte way&nbsp;– it’s about how we work together, guided by our values, to give clinicians the insights they need to help patients make life-changing decisions.&nbsp; Our Values: We Seek A Better Way: We innovate boldly, learn from our setbacks, and are resilient in our pursuit to transform cancer care We Make It Happen: We act with urgency, commit to quality, and bring fun to our hard work We Are Stronger Together:&nbsp;We collaborate openly, seek to understand, and celebrate our wins We Care Deeply: We embrace our differences, do the right thing, and encourage each other &nbsp;&nbsp; The Position: We are seeking a highly skilled Software Engineer with expertise in Python, AWS, and coding best practices. The ideal candidate will have a strong background in software development, cloud computing. You will be responsible for developing and maintaining scalable software solutions that power our products and services. This is a onsite/hybrid position based in our San Diego, CA office.&nbsp; &nbsp; Key Responsibilities: Design, develop, and maintain high-quality software solutions using Python. Utilize AWS services to build, deploy, and manage applications in the cloud. Has strong knowledge of cloud data engineering principles and manages Python based data pipelines. Write clean, maintainable, and efficient code. Collaborate with cross-functional teams to define, design, and ship new features. Troubleshoot and resolve complex technical issues and bugs. Perform code reviews and provide constructive feedback to peers. Stay up-to-date with the latest industry trends and technologies to ensure our solutions remain current and competitive. &nbsp; Who You Are: .Bachelor’s degree in Computer Science, Engineering, or a related field. 4+ years of experience in software development. Proven experience delivering solutions making use of AWS. Understanding of software development best practices, including design patterns, coding standards, ELT/ETL standards, and code reviews. Excellent problem-solving skills and the ability to work independently or as part of a team. Strong communication skills and the ability to articulate complex technical concepts to non-technical stakeholders Preferred Skills: Experience with web development technologies such as Node.js, React, Vue.js, or similar. Familiarity with microservices architecture and RESTful API design. Familiarity with CI/CD concepts and tools like Jenkins, GitLab CI, CircleCI, or similar Experience with containerization and orchestration tools such as Docker and Kubernetes. Knowledge of database systems, both SQL and NoSQL. Experience with monitoring and logging tools like CloudWatch, ELK Stack, or similar. Prior experience in a senior or lead engineering role. #LI-Hybrid &nbsp;The final salary offered to a successful candidate will be dependent on several factors that may include but are not limited to the type and length of experience within the job, type and length of experience within the industry, education, etc. Base pay is one part of the Total Package that is provided to compensate and recognize employees for their work, and this role may be eligible for additional discretionary bonuses/incentives, and restricted stock units. Veracyte is a multi-state employer, and this salary range may not reflect positions that work in other states.Pay range$150,000&mdash;$165,000 USD&nbsp; What We Can Offer You Veracyte is a growing company that offers significant career opportunities if you are curious, driven, patient-oriented and aspire to help us build a great company. We offer competitive compensation and benefits, and are committed to fostering an inclusive workforce, where diverse backgrounds are represented, engaged, and empowered to drive innovative ideas and decisions. We are thrilled to be recognized as a 2024 Certified™ Great Place to Work® in both the US and Israel - a testament to our dynamic, inclusive, and inspiring workplace where passion meets purpose. &nbsp; About Veracyte Veracyte&nbsp;(Nasdaq: VCYT) is a global genomic diagnostics company that improves patient care by providing answers to clinical questions, informing diagnosis and treatment decisions throughout the patient journey in cancer and other diseases. The company’s growing menu of genomic tests leverage advances in genomic science and technology, enabling patients to avoid risky, costly diagnostic procedures and quicken time to appropriate treatment. The company’s tests in lung cancer, prostate cancer, breast cancer, thyroid cancer, bladder cancer and idiopathic pulmonary fibrosis are available to patients and its lymphoma subtyping and renal cancer tests are in development. With Veracyte’s exclusive global license to a best-in-class diagnostics instrument platform, the company is positioned to deliver its tests to patients worldwide.&nbsp;Veracyte&nbsp;is based in&nbsp;South San Francisco, California. For more information, please visit&nbsp;www.veracyte.com and follow the company on X (Formerly Twitter). Veracyte, Inc. is an Equal Opportunity Employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status or disability status. Veracyte participates in E-Verify in the United States. View our&nbsp;CCPA Disclosure Notice. If you receive any suspicious alerts or communications through LinkedIn or other online job sites for any position at Veracyte, please exercise caution and promptly report any concerns to careers@veracyte.com

Software Development Engineer

At Veracyte, we offer exciting career opportunities for those interested in joining a pioneering team that is committed to transforming cancer care for patients across the globe. Working at Veracyte enables our employees to not only make a meaningful impact on the lives of patients, but to also learn and grow within a purpose driven&nbsp;environment. This is what we call the Veracyte way&nbsp;– it’s about how we work together, guided by our values, to give clinicians the insights they need to help patients make life-changing decisions.&nbsp; Our Values: We Seek A Better Way: We innovate boldly, learn from our setbacks, and are resilient in our pursuit to transform cancer care We Make It Happen: We act with urgency, commit to quality, and bring fun to our hard work We Are Stronger Together:&nbsp;We collaborate openly, seek to understand, and celebrate our wins We Care Deeply: We embrace our differences, do the right thing, and encourage each other &nbsp;The Position: Primarily responsibility for receiving and accessioning specimens, handling specimen documentation, and data entry of requisitions. They are also responsible for keeping the lab in a clean and orderly condition. Specimen Processor I are knowledgeable in sample integrity issues and are a resource to others in the lab. They maintain flexibility regarding work schedules including daily assignments, holiday schedules, and days of the week as determined by business need.&nbsp; This is an onsite role in the South San Francisco office. The schedule is Tuesday - Saturday, 9am - 5:30pm. ESSENTIAL DUTIES AND RESPONSIBILITIES: include the following. Other duties may be assigned.&nbsp; Accessioning clinical specimens upon receipt and entering data into LIS system. Specimen verification, labeling, tracking, and all related clerical functions. Capable of identifying specimen processing problems that may adversely affect the reporting of test results and immediately notifying the supervisor. Documenting all corrective actions taken when test systems deviate from the laboratory's established performance specifications. Following the laboratory's established policies and procedures. Understanding of compliance regulations related to test ordering.&nbsp; Compliant with company policies, procedures, safety requirements and regulations. Contributing to the safety of the laboratory operations by complying with established safety procedures and making recommendations for improvement. Engaging in training and competency assessments. Attending and participating in department meetings. Participating in activities associated with regulatory compliance and inspections. Assisting in continuous improvement activities/projects. Assisting in research and validation activities. Helping perform weekly, monthly, and other periodic room and equipment maintenance procedures in accordance with standard operating procedures. Helping track and stock laboratory supplies. General clean-up tasks, e.g. break down and trash shipping boxes/packaging, disinfect lab benches and surfaces, and put away supplies. Working cooperatively in a team environment and supporting senior laboratory and management staff. Working cross-functionally with Customer Care regarding specimen issues and Accessioning requests. • Complete other related administrative duties, including printing, copying, filing, faxing, and quality control of spreadsheets. REQUIREMENTS: QUALIFICATIONS&nbsp;To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skills and/or abilities required. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions.&nbsp; EDUCATION and/or EXPERIENCE 0-2 years of accessioning experience and/or in a lab setting High school diploma or equivalent required Bachelor’s degree preferred. Good verbal and written communication skills. The ability to navigate efficiently through, or have familiarity with, various laboratory information systems (LIS) and have proficiency in Microsoft Office products (Excel, Word, Access and PowerPoint). Good judgment and problem-solving skills Excellent teamwork and collaborations skills Ability to work independently PHYSICAL REQUIREMENTS Repetitive movement of hands, arms and legs Repetitive movement of fingers (typing and/or writing) Sitting, with occasional walking, standing, stooping and moving about Talking and hearing Occasionally required to lift up to 25 pounds The final salary offered to a successful candidate will be dependent on several factors that may include but are not limited to the type and length of experience within the job, type and length of experience within the industry, education, etc. Base pay is one part of the Total Package that is provided to compensate and recognize employees for their work, and this role may be eligible for additional discretionary bonuses/incentives, and restricted stock units. Veracyte is a multi-state employer, and this salary range may not reflect positions that work in other states.Pay range$28&mdash;$31 USD&nbsp; What We Can Offer You Veracyte is a growing company that offers significant career opportunities if you are curious, driven, patient-oriented and aspire to help us build a great company. We offer competitive compensation and benefits, and are committed to fostering an inclusive workforce, where diverse backgrounds are represented, engaged, and empowered to drive innovative ideas and decisions. We are thrilled to be recognized as a 2024 Certified™ Great Place to Work® in both the US and Israel - a testament to our dynamic, inclusive, and inspiring workplace where passion meets purpose. &nbsp; About Veracyte Veracyte&nbsp;(Nasdaq: VCYT) is a global genomic diagnostics company that improves patient care by providing answers to clinical questions, informing diagnosis and treatment decisions throughout the patient journey in cancer and other diseases. The company’s growing menu of genomic tests leverage advances in genomic science and technology, enabling patients to avoid risky, costly diagnostic procedures and quicken time to appropriate treatment. The company’s tests in lung cancer, prostate cancer, breast cancer, thyroid cancer, bladder cancer and idiopathic pulmonary fibrosis are available to patients and its lymphoma subtyping and renal cancer tests are in development. With Veracyte’s exclusive global license to a best-in-class diagnostics instrument platform, the company is positioned to deliver its tests to patients worldwide.&nbsp;Veracyte&nbsp;is based in&nbsp;South San Francisco, California. For more information, please visit&nbsp;www.veracyte.com and follow the company on X (Formerly Twitter). Veracyte, Inc. is an Equal Opportunity Employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status or disability status. Veracyte participates in E-Verify in the United States. View our&nbsp;CCPA Disclosure Notice. If you receive any suspicious alerts or communications through LinkedIn or other online job sites for any position at Veracyte, please exercise caution and promptly report any concerns to careers@veracyte.com

Specimen Processor

At Veracyte, we offer exciting career opportunities for those interested in joining a pioneering team that is committed to transforming cancer care for patients across the globe. Working at Veracyte enables our employees to not only make a meaningful impact on the lives of patients, but to also learn and grow within a purpose driven&nbsp;environment. This is what we call the Veracyte way&nbsp;– it’s about how we work together, guided by our values, to give clinicians the insights they need to help patients make life-changing decisions.&nbsp; Our Values: We Seek A Better Way: We innovate boldly, learn from our setbacks, and are resilient in our pursuit to transform cancer care We Make It Happen: We act with urgency, commit to quality, and bring fun to our hard work We Are Stronger Together:&nbsp;We collaborate openly, seek to understand, and celebrate our wins We Care Deeply: We embrace our differences, do the right thing, and encourage each other &nbsp;The Position: This can be a hybrid position based out of our San Diego office, South San Francisco office, or remote.&nbsp; We are seeking an experienced and motivated Bioinformatics Scientist to join our Bioinformatics and Data Science Team focused on developing regulated diagnostics products. The ideal candidate will bring deep expertise in NGS technologies with a strong understanding of regulatory environments including CAP/CLIA and IVD product development. The successful candidate will play a crucial role in designing, developing, and optimizing our next generation of genomic assays. This position requires a unique blend of expertise in bioinformatics, extensive experience in assay optimization, analytical validation, strong skills in analytical pipeline development, automation and optimization, a deep understanding of molecular biology, and a passion for transforming complex biological data into actionable insights. KEY RESPONSIBILITIES: Lead bioinformatics design, development and validation efforts in assay development for new and on-market products. As part of project core teams, this individual must be responsible for coordinating planning, execution, and delivery within timelines and budget constraints. Apply leading edge knowledge in bioinformatics, genomics, and assay technologies, to contribute to development of company's concepts and principles and to achieve assay development objectives in creative and effective ways. Drive development study design and all analysis for assay development effort in collaboration with cross-functional teams. Develop statistical and machine learning techniques to comprehensively evaluate assay performance and create optimization strategies. Communicate analysis results, methodologies, and scientific findings to internal teams, external collaborators, and stakeholders. Develop scalable, production-grade workflows for high-throughput NGS data analysis using AWS and containerized environments. Facilitate successful production pipeline deployment by working closely with infrastructure and engineering teams Ensure compliance with regulatory standards (CAP/CLIA, FDA, IVDR) throughout the bioinformatics development lifecycle, including rigorous testing and documentation. Contribute to regulatory submissions and audits by providing technical documentation and validation reports. Provide scientific guidance and mentorship to junior bioinformatics team members. Who You Are: REQUIRED EXPERIENCE: PhD or MS in bioinformatics, computational biology, or an adjacent data science field, such as biostatistics, statistics or computer science. Proven experience - A minimum of 6 -7 years of experience in bioinformatics analysis, algorithm development, and pipeline implementation. Thorough understanding of NGS technologies and various methods for library preparation (WGS, enrichment, RNA-Seq, methylation, etc.). Proficiency in quantitative transcriptomics from NGS or expression microarray data in human disease/biology specifically, such as differential expression, dimension reduction, expression-based classifier development, RNA-based signatures, cell type deconvolution. Proficiency in machine learning, development of novel bioinformatics methodologies, and algorithms development, including benchmarking of computational methods. Proven experience developing and deploying bioinformatics workflows in AWS (e.g., EC2, S3, Step Functions, Batch, Lambda, etc.). Strong proficiency in Python, including experience with testing frameworks and SDLC best practices. Close collaboration with Quality and Regulatory Affairs team on assay and analysis pipeline development and verification. Demonstrated record of technical and scientific leadership, ownership, and independent work. RELEVANT EXPERIENCE (preferred but not required): Track record of working with wet lab scientists on iterative experiment design, execution, analysis, and interpretation as a tightly integrated team. Proficiency in genomics, sequence analysis, and secondary analysis, such as variant calling (e.g., SNVs/MNVs/indels, CNV, structural variants), NGS QC, splicing, circular nucleic acids. Strong understanding of germline and somatic mutation processes leading to complex variation and genome-wide biomarkers with potential clinical utility, such as TMB, mutational signatures, LOH. Working knowledge of R. Experience with relational and non-relational database technologies is a plus. Excellent communicator about complex technical topics in an interdisciplinary setting, especially by using data visualizations and diagrams. Excellent technical problem solving and troubleshooting skills. &nbsp; &nbsp; #LI-Hybrid &nbsp;The final salary offered to a successful candidate will be dependent on several factors that may include but are not limited to the type and length of experience within the job, type and length of experience within the industry, education, etc. Base pay is one part of the Total Package that is provided to compensate and recognize employees for their work, and this role may be eligible for additional discretionary bonuses/incentives, and restricted stock units. Veracyte is a multi-state employer, and this salary range may not reflect positions that work in other states.Pay range$170,000&mdash;$180,000 USD&nbsp; What We Can Offer You Veracyte is a growing company that offers significant career opportunities if you are curious, driven, patient-oriented and aspire to help us build a great company. We offer competitive compensation and benefits, and are committed to fostering an inclusive workforce, where diverse backgrounds are represented, engaged, and empowered to drive innovative ideas and decisions. We are thrilled to be recognized as a 2024 Certified™ Great Place to Work® in both the US and Israel - a testament to our dynamic, inclusive, and inspiring workplace where passion meets purpose. &nbsp; About Veracyte Veracyte&nbsp;(Nasdaq: VCYT) is a global genomic diagnostics company that improves patient care by providing answers to clinical questions, informing diagnosis and treatment decisions throughout the patient journey in cancer and other diseases. The company’s growing menu of genomic tests leverage advances in genomic science and technology, enabling patients to avoid risky, costly diagnostic procedures and quicken time to appropriate treatment. The company’s tests in lung cancer, prostate cancer, breast cancer, thyroid cancer, bladder cancer and idiopathic pulmonary fibrosis are available to patients and its lymphoma subtyping and renal cancer tests are in development. With Veracyte’s exclusive global license to a best-in-class diagnostics instrument platform, the company is positioned to deliver its tests to patients worldwide.&nbsp;Veracyte&nbsp;is based in&nbsp;South San Francisco, California. For more information, please visit&nbsp;www.veracyte.com and follow the company on X (Formerly Twitter). Veracyte, Inc. is an Equal Opportunity Employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status or disability status. Veracyte participates in E-Verify in the United States. View our&nbsp;CCPA Disclosure Notice. If you receive any suspicious alerts or communications through LinkedIn or other online job sites for any position at Veracyte, please exercise caution and promptly report any concerns to careers@veracyte.com

Sr. Bioinformatics Scientist

At Veracyte, we offer exciting career opportunities for those interested in joining a pioneering team that is committed to transforming cancer care for patients across the globe. Working at Veracyte enables our employees to not only make a meaningful impact on the lives of patients, but to also learn and grow within a purpose driven&nbsp;environment. This is what we call the Veracyte way&nbsp;– it’s about how we work together, guided by our values, to give clinicians the insights they need to help patients make life-changing decisions.&nbsp; Our Values: We Seek A Better Way: We innovate boldly, learn from our setbacks, and are resilient in our pursuit to transform cancer care We Make It Happen: We act with urgency, commit to quality, and bring fun to our hard work We Are Stronger Together:&nbsp;We collaborate openly, seek to understand, and celebrate our wins We Care Deeply: We embrace our differences, do the right thing, and encourage each other &nbsp;The Position: We are seeking a talented and experienced AI/ML data scientist to join our Veracyte’s Data Science team. This position offers a unique opportunity to work with experienced professionals to drive research and develop new diagnostic products employing one of the world’s largest clinical cancer databases, encompassing multi-platform digital pathology, genomic and clinical outcome data. &nbsp; The successful candidate will develop digital pathology AI models for a wide range of clinical and pathology outcomes by applying and adapting state-of-the-art vision/vision-language foundation models to whole-slide images (WSIs). As a Sr. Scientist at Veracyte, the candidate will be expected to show technical leadership in this field and independently drive project execution and completion. This work will be conducted in close collaboration with other teams, including internal medical and business development teams, as well as key opinion leaders, with whom we collaborate on identifying relevant data, and developing computer vision models. The ability to explain AI/ML concepts to both experts and non-experts, including formal presentation, academic writing, and generation of publication-quality figures will be key necessary talents. The ideal candidate is passionate about data, eager to learn independently, and possesses strong analytical, problem-solving, and storytelling skills. &nbsp; KEY RESPONSIBILITIES: &nbsp; Develop digital pathology AI (DPAI) models with WSI data to predict clinical outcome and pathological/morphologic features, including adapting open-source state-of-the-art AI foundation models to Veracyte’s data. &nbsp; Evaluate and analyze DPAI models with respect to clinical, pathological and genomic outcomes or features, with a view to linking explainability of model features to biology.&nbsp; Collaborate with both internal and external partners to understand the clinical and business requirements for given products and tailor algorithms accordingly. &nbsp; &nbsp;Work with bioinformatician, statistician, and medical experts to document projects, including generating analyses and visualizations for publication in peer-reviewed journals. &nbsp; Who You Are: PhD in Data Science, Machine Learning, Applied Math or equivalent field. &nbsp; 8+ years of experience of data/applied scientist role or equivalent &nbsp; Expert in Python or equivalent language for AI/ML development in the context of computer vision / DPAI (this includes data manipulation and preparation.)&nbsp; Proficient in statistical analysis, especially in survival modelling and hypothesis testing (i.e., multivariate regression modelling with interaction effects).&nbsp; Experience working in cloud computing environments (AWS preferred). &nbsp; Demonstrated proficiency in summarizing and communicating findings from data, including an attention to detail when sharing findings.&nbsp; Ability to work effectively in a fast-paced and collaborative environment. &nbsp; Eagerness to learn new technologies and adapt to evolving requirements. &nbsp; RELEVANT EXPERIENCE (preferred but not required): &nbsp; Knowledge of cancer biology&nbsp; Proficiency with documentation and submission in regulated diagnostic environments (LDT or IVD).&nbsp; Experience working with real world clinical data.&nbsp; LOCATION: &nbsp; This is a remote friendly position. &nbsp; On-site desk-space is available in South San Francisco or San Diego. &nbsp; &nbsp; &nbsp; #LI-Hybrid, #LI-Remote &nbsp;The final salary offered to a successful candidate will be dependent on several factors that may include but are not limited to the type and length of experience within the job, type and length of experience within the industry, education, etc. Base pay is one part of the Total Package that is provided to compensate and recognize employees for their work, and this role may be eligible for additional discretionary bonuses/incentives, and restricted stock units. Veracyte is a multi-state employer, and this salary range may not reflect positions that work in other states.Pay range$186,000&mdash;$243,000 USD&nbsp; What We Can Offer You Veracyte is a growing company that offers significant career opportunities if you are curious, driven, patient-oriented and aspire to help us build a great company. We offer competitive compensation and benefits, and are committed to fostering an inclusive workforce, where diverse backgrounds are represented, engaged, and empowered to drive innovative ideas and decisions. We are thrilled to be recognized as a 2024 Certified™ Great Place to Work® in both the US and Israel - a testament to our dynamic, inclusive, and inspiring workplace where passion meets purpose. &nbsp; About Veracyte Veracyte&nbsp;(Nasdaq: VCYT) is a global genomic diagnostics company that improves patient care by providing answers to clinical questions, informing diagnosis and treatment decisions throughout the patient journey in cancer and other diseases. The company’s growing menu of genomic tests leverage advances in genomic science and technology, enabling patients to avoid risky, costly diagnostic procedures and quicken time to appropriate treatment. The company’s tests in lung cancer, prostate cancer, breast cancer, thyroid cancer, bladder cancer and idiopathic pulmonary fibrosis are available to patients and its lymphoma subtyping and renal cancer tests are in development. With Veracyte’s exclusive global license to a best-in-class diagnostics instrument platform, the company is positioned to deliver its tests to patients worldwide.&nbsp;Veracyte&nbsp;is based in&nbsp;South San Francisco, California. For more information, please visit&nbsp;www.veracyte.com and follow the company on X (Formerly Twitter). Veracyte, Inc. is an Equal Opportunity Employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status or disability status. Veracyte participates in E-Verify in the United States. View our&nbsp;CCPA Disclosure Notice. If you receive any suspicious alerts or communications through LinkedIn or other online job sites for any position at Veracyte, please exercise caution and promptly report any concerns to careers@veracyte.com

Sr. Data Scientist

At Veracyte, we offer exciting career opportunities for those interested in joining a pioneering team that is committed to transforming cancer care for patients across the globe. Working at Veracyte enables our employees to not only make a meaningful impact on the lives of patients, but to also learn and grow within a purpose driven&nbsp;environment. This is what we call the Veracyte way&nbsp;– it’s about how we work together, guided by our values, to give clinicians the insights they need to help patients make life-changing decisions.&nbsp; Our Values: We Seek A Better Way: We innovate boldly, learn from our setbacks, and are resilient in our pursuit to transform cancer care We Make It Happen: We act with urgency, commit to quality, and bring fun to our hard work We Are Stronger Together:&nbsp;We collaborate openly, seek to understand, and celebrate our wins We Care Deeply: We embrace our differences, do the right thing, and encourage each other &nbsp;The Position: As a Senior QA Specialist you will be part of the IVD Quality team that is responsible of the development and implementation of a right sized Quality Management System that includes quality processes and procedures, automated systems, and ensuring compliance with all applicable internal, domestic, and international quality regulations, including ISO 13485, IVDR, and others global regulations and standards.&nbsp; This is a hybrid role (remote and in office at least 3 days a week) and is based out of our headquarters in South San Francisco (SSF), California, United States. &nbsp; Responsibilities Support the development, implementation, and maintenance of the Quality Management System (QMS) in accordance with ISO 13485 and applicable standards and regulations for in vitro diagnostic (IVD) products Drive implementation projects for critical QMS elements (eQMS rollout, CAPA process, supplier qualification program, design control workflows) Develop and update QMS processes and documentation: SOPs, work instructions, templates (DMR/DHF, CAPA, change control, complaint handling, supplier quality, document control, risk management etc.) in accordance with ISO 13485 and IVDR requirements Serve as a Sr. QA subject-matter-expert supporting product development, transfer to CMO, and post market activities for IVDs Support design control and technical documentation: review design inputs/outputs, verification and validation protocols and reports, design history files (DHFs), and IVDR technical documentation Support process and equipment qualifications (IQ/OQ/PQ) and software validation activities as required Manage supplier qualification and ongoing supplier quality monitoring; perform supplier audits and oversee supplier corrective actions Implement and maintain risk management per ISO 14971: facilitate risk assessments, ensure residual risk acceptance, and link risk to design changes and CAPAs Participate in internal audits and support external audits (notified body, regulatory inspections), prepare audit responses, and lead remediation activities Develop, track, and report QMS metrics and KPIs for management review Lead and coordinate CAPA investigations and corrective/preventive actions — ensure root-cause analysis, implementation, and verification of effectiveness within timelines Manage nonconforming product (NCRs), deviations, change control, and product dispositions, ensuring appropriate investigation and documentation Oversee complaint handling: lead investigations, support trend analysis and PMS Other duties as assigned Who You Are: Qualifications Bachelor’s degree in Life Sciences, Engineering, Biomedical Engineering, Biotechnology, or related technical field 5+ years hands‑on quality assurance experience in the medical device or in‑vitro diagnostic (IVD) industry In‑depth knowledge of in‑vitro diagnostic device quality requirements, including ISO 13485:2016, IVDR (EU 2017/746) and, ISO 14971:2019 risk management Experience implementing and operating a QMS to ISO 13485:2016 Experience with design control, risk management (ISO 14971), verification &amp; validation, CAPA, change control, complaint handling, and supplier quality Experience conducting internal audits and supporting external ISO audits or third-party assessments Strong written and verbal communication skills; demonstrated ability to author clear SOPs, technical documents, and audit responses Strong organization skills to manage multiple simultaneous projects in a fast-paced environment Attention to detail in understanding and documenting complex quality issues Strong writing skills to summarize complex issues clearly and accurately Strong communication, problem-solving, and motivational skills Highly organized, self-motivated, and comfortable working in a fast-paced IVD environment ISO 13485 Lead Auditor or equivalent lead auditor certificate is preferred &nbsp; #LI-HybridThe final salary offered to a successful candidate will be dependent on several factors that may include but are not limited to the type and length of experience within the job, type and length of experience within the industry, education, etc. Base pay is one part of the Total Package that is provided to compensate and recognize employees for their work, and this role may be eligible for additional discretionary bonuses/incentives, and restricted stock units. Veracyte is a multi-state employer, and this salary range may not reflect positions that work in other states.Pay range$117,000&mdash;$130,000 USD&nbsp; What We Can Offer You Veracyte is a growing company that offers significant career opportunities if you are curious, driven, patient-oriented and aspire to help us build a great company. We offer competitive compensation and benefits, and are committed to fostering an inclusive workforce, where diverse backgrounds are represented, engaged, and empowered to drive innovative ideas and decisions. We are thrilled to be recognized as a 2024 Certified™ Great Place to Work® in both the US and Israel - a testament to our dynamic, inclusive, and inspiring workplace where passion meets purpose. &nbsp; About Veracyte Veracyte&nbsp;(Nasdaq: VCYT) is a global genomic diagnostics company that improves patient care by providing answers to clinical questions, informing diagnosis and treatment decisions throughout the patient journey in cancer and other diseases. The company’s growing menu of genomic tests leverage advances in genomic science and technology, enabling patients to avoid risky, costly diagnostic procedures and quicken time to appropriate treatment. The company’s tests in lung cancer, prostate cancer, breast cancer, thyroid cancer, bladder cancer and idiopathic pulmonary fibrosis are available to patients and its lymphoma subtyping and renal cancer tests are in development. With Veracyte’s exclusive global license to a best-in-class diagnostics instrument platform, the company is positioned to deliver its tests to patients worldwide.&nbsp;Veracyte&nbsp;is based in&nbsp;South San Francisco, California. For more information, please visit&nbsp;www.veracyte.com and follow the company on X (Formerly Twitter). Veracyte, Inc. is an Equal Opportunity Employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status or disability status. Veracyte participates in E-Verify in the United States. View our&nbsp;CCPA Disclosure Notice. If you receive any suspicious alerts or communications through LinkedIn or other online job sites for any position at Veracyte, please exercise caution and promptly report any concerns to careers@veracyte.com

Sr. Quality Specialist

At Veracyte, we offer exciting career opportunities for those interested in joining a pioneering team that is committed to transforming cancer care for patients across the globe. Working at Veracyte enables our employees to not only make a meaningful impact on the lives of patients, but to also learn and grow within a purpose driven&nbsp;environment. This is what we call the Veracyte way&nbsp;– it’s about how we work together, guided by our values, to give clinicians the insights they need to help patients make life-changing decisions.&nbsp; Our Values: We Seek A Better Way: We innovate boldly, learn from our setbacks, and are resilient in our pursuit to transform cancer care We Make It Happen: We act with urgency, commit to quality, and bring fun to our hard work We Are Stronger Together:&nbsp;We collaborate openly, seek to understand, and celebrate our wins We Care Deeply: We embrace our differences, do the right thing, and encourage each other &nbsp;The Position: This position will be based in the Nordics, ideally in Norway, Sweden or Denmark.&nbsp; The Senior Regional Business Manager is responsible for first establishing and then growing Veracyte's Diagnostic business in his/her area of responsibility. This individual works closely with the General Manager to define Veracyte's commercial plan for his/her area of responsibility and its execution in assigned territory. This individual leads the Nordics commercial activities of the diagnostic version of the nCounter platform and in vitro diagnostic assays, beginning with the breast cancer assay, Prosigna and future launches. This individual has direct responsibility for sales revenue. This individual works with the General Manager to maximize sales revenues from National Centers and key Private Centers, and drives growth by articulating a thoughtful, evidence-based rationale for how practicing Oncologists and Pathologists can use Veracyte's diagnostic tests to improve outcomes whilst also reducing costs through the accurate diagnosis and appropriate treatment of disease. As such, this individual must be comfortable in dialoguing with the most senior thought leaders and decision-makers in the field of Oncology, and will also need to analyze the market and detect the best and faster opportunities to develop the business. In addition, this individual works closely with the marketing and medical teams in order to detect, organize and execute marketing activities (congresses, tradeshows, seminars, etc.) at a regional and global level.&nbsp; &nbsp; Essential Functions: Focus on successfully launching and maintaining Prosigna assay(s) and other launch diagnostic products in your sales region, maximizing sales, developing the market and increasing the test demand Develop a go-to-market strategy to launch diagnostic tests in key Private Centers and in Academic Hospitals including securing reimbursement in coordination with regional market access teams. Develop commercial and activities plan for his/her area of responsibility in close collaboration with the medical team responsible including tender management responsibilities and business development opportunities Be responsible for own performance, checking own progress against goals established in collaboration with line manager Communicating feedback promptly with line manager and addressing issues accordingly Make Prosigna known through marketing activities to the breast cancer community and attend the most relevant congresses and seminars. Marketing activities should be aligned with the Regional and global strategy and tactics, aligned with budget allocations and after medical affairs consultation (for relevance and compliance) Develop commercial activities related to Diagnostic Business for Veracyte in assigned territory, in line with the strategy defined by IVD General Manager and approved by Veracyte Leadership; quality policies of the company; local specific regulations and both local and global regulatory matters Regular travel across assigned territory region is required Who You Are: 6+ years of commercial experience, including revenue responsibility and a proven track record of successfully launching Oncology drugs and/or diagnostics, ideally in lean and fast-paced organizations Experience in Sales and Market Development especially in growing Oncology businesses in Norway and Nordics region. Candidates who have played a key role in launching a commercially successful drug, molecular diagnostic or have experience in the sales of a companion diagnostic to the Oncology community are of particular interest. Communication skills to work effectively with external constituents, such as clinicians, KOLs, as well as with internal stakeholders Knowledge of diagnostic market in region Specific experience in product or services in the diagnosis or treatment of breast and /or prostate cancer Native or resident of territory region, demonstrating affinity and knowledge of the country, its culture and people Strong influencing and convincing skills and experience with regards to Oncologists and Pathologists Substantiated track record of negotiating and closing deals with hospital and Health Authorities. Flexibility and cultural sensitivity to work in a rapidly growing yet still small company Able to operate autonomously yet within a structured corporate environment Previous experience of working with international headquarters is a plus. Driven, self-motivated, independent, dependable and passionate individual with strong leadership ability and excellent project and time management skills Excellent interpersonal, communication and presentation skills Outstanding business acumen and entrepreneurial sense and proven excellence with regards to organizational, analytical and problem-solving skills. Good interaction with colleagues, supportive of team work Scientific background strongly preferred (biologist, biochemistry, pharmacy, medicine, etc.) Commercial diagnostics or Pharmaceutical experience is strongly preferred &nbsp; #LI-Remote &nbsp;&nbsp; What We Can Offer You Veracyte is a growing company that offers significant career opportunities if you are curious, driven, patient-oriented and aspire to help us build a great company. We offer competitive compensation and benefits, and are committed to fostering an inclusive workforce, where diverse backgrounds are represented, engaged, and empowered to drive innovative ideas and decisions. We are thrilled to be recognized as a 2024 Certified™ Great Place to Work® in both the US and Israel - a testament to our dynamic, inclusive, and inspiring workplace where passion meets purpose. &nbsp; About Veracyte Veracyte&nbsp;(Nasdaq: VCYT) is a global genomic diagnostics company that improves patient care by providing answers to clinical questions, informing diagnosis and treatment decisions throughout the patient journey in cancer and other diseases. The company’s growing menu of genomic tests leverage advances in genomic science and technology, enabling patients to avoid risky, costly diagnostic procedures and quicken time to appropriate treatment. The company’s tests in lung cancer, prostate cancer, breast cancer, thyroid cancer, bladder cancer and idiopathic pulmonary fibrosis are available to patients and its lymphoma subtyping and renal cancer tests are in development. With Veracyte’s exclusive global license to a best-in-class diagnostics instrument platform, the company is positioned to deliver its tests to patients worldwide.&nbsp;Veracyte&nbsp;is based in&nbsp;South San Francisco, California. For more information, please visit&nbsp;www.veracyte.com and follow the company on X (Formerly Twitter). Veracyte, Inc. is an Equal Opportunity Employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status or disability status. Veracyte participates in E-Verify in the United States. View our&nbsp;CCPA Disclosure Notice. If you receive any suspicious alerts or communications through LinkedIn or other online job sites for any position at Veracyte, please exercise caution and promptly report any concerns to careers@veracyte.com

Sr. Regional Business Manager - Nordics

At Veracyte, we offer exciting career opportunities for those interested in joining a pioneering team that is committed to transforming cancer care for patients across the globe. Working at Veracyte enables our employees to not only make a meaningful impact on the lives of patients, but to also learn and grow within a purpose driven&nbsp;environment. This is what we call the Veracyte way&nbsp;– it’s about how we work together, guided by our values, to give clinicians the insights they need to help patients make life-changing decisions.&nbsp; Our Values: We Seek A Better Way: We innovate boldly, learn from our setbacks, and are resilient in our pursuit to transform cancer care We Make It Happen: We act with urgency, commit to quality, and bring fun to our hard work We Are Stronger Together:&nbsp;We collaborate openly, seek to understand, and celebrate our wins We Care Deeply: We embrace our differences, do the right thing, and encourage each other &nbsp;The Position: We are seeking a highly skilled Senior Software Development Engineer with expertise in C#/Python, AWS, and CI/CD practices. The ideal candidate will have a strong background in software development, cloud computing, and continuous integration/continuous deployment methodologies. You will be responsible for designing, developing, and maintaining scalable software solutions that power our products and services. This position is a hybrid position located in our Haifa office. We are also open to remote for candidates.Key Responsibilities Design, develop, and maintain high-quality software solutions using C# and Python. Architect and lead the implementation of cloud-based applications and services on AWS. Develop and manage CI/CD pipelines to ensure seamless integration and deployment of code. Collaborate with cross-functional teams to define, design, implement, test and ship new features. Troubleshoot and resolve complex technical issues and bugs. Mentor junior engineers and provide technical guidance and code reviews. Stay up-to-date with the latest industry trends and technologies to ensure our solutions remain current and competitive. Who You Are: Bachelor’s degree in Computer Science, and a minimum of 10 years of hands-on experience in high-level programming languages. Prior experience in a senior or lead engineering role. Proven experience delivering solutions using public clouds, preferably AWS. Experience with microservices architecture. Experience with containerization and orchestration tools such as Docker and Kubernetes. Proficiency in building and managing CI/CD pipelines. Strong understanding of software development best practices, including design patterns, coding standards, and code reviews. Excellent problem-solving skills and the ability to work independently or as part of a team. Strong communication skills and the ability to articulate complex technical concepts to non-technical stakeholders. Preferred Skills Experience with Software Development Lifecycle (SDLC) frameworks and processes, preferably using Microsoft Azure DevOps. Experience with Software-as-a-Medical Device (SaMD) development. Knowledge of SQL-based database systems. Experience with observability frameworks like CloudWatch, OpenTelemetry, DataDog, Dynatrace and others. #LI-Hybrid &nbsp;&nbsp; What We Can Offer You Veracyte is a growing company that offers significant career opportunities if you are curious, driven, patient-oriented and aspire to help us build a great company. We offer competitive compensation and benefits, and are committed to fostering an inclusive workforce, where diverse backgrounds are represented, engaged, and empowered to drive innovative ideas and decisions. We are thrilled to be recognized as a 2024 Certified™ Great Place to Work® in both the US and Israel - a testament to our dynamic, inclusive, and inspiring workplace where passion meets purpose. &nbsp; About Veracyte Veracyte&nbsp;(Nasdaq: VCYT) is a global genomic diagnostics company that improves patient care by providing answers to clinical questions, informing diagnosis and treatment decisions throughout the patient journey in cancer and other diseases. The company’s growing menu of genomic tests leverage advances in genomic science and technology, enabling patients to avoid risky, costly diagnostic procedures and quicken time to appropriate treatment. The company’s tests in lung cancer, prostate cancer, breast cancer, thyroid cancer, bladder cancer and idiopathic pulmonary fibrosis are available to patients and its lymphoma subtyping and renal cancer tests are in development. With Veracyte’s exclusive global license to a best-in-class diagnostics instrument platform, the company is positioned to deliver its tests to patients worldwide.&nbsp;Veracyte&nbsp;is based in&nbsp;South San Francisco, California. For more information, please visit&nbsp;www.veracyte.com and follow the company on X (Formerly Twitter). Veracyte, Inc. is an Equal Opportunity Employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status or disability status. Veracyte participates in E-Verify in the United States. View our&nbsp;CCPA Disclosure Notice. If you receive any suspicious alerts or communications through LinkedIn or other online job sites for any position at Veracyte, please exercise caution and promptly report any concerns to careers@veracyte.com

Sr. Software Development Engineer

At Veracyte, we offer exciting career opportunities for those interested in joining a pioneering team that is committed to transforming cancer care for patients across the globe. Working at Veracyte enables our employees to not only make a meaningful impact on the lives of patients, but to also learn and grow within a purpose driven&nbsp;environment. This is what we call the Veracyte way&nbsp;– it’s about how we work together, guided by our values, to give clinicians the insights they need to help patients make life-changing decisions.&nbsp; Our Values: We Seek A Better Way: We innovate boldly, learn from our setbacks, and are resilient in our pursuit to transform cancer care We Make It Happen: We act with urgency, commit to quality, and bring fun to our hard work We Are Stronger Together:&nbsp;We collaborate openly, seek to understand, and celebrate our wins We Care Deeply: We embrace our differences, do the right thing, and encourage each other &nbsp;The Position: &nbsp; Veracyte is seeking an experienced and highly motivated Equipment Supervisor to join our Equipment Engineering and Operations team at our South San Francisco headquarters. Under the general direction of the Manager of Equipment Engineering and Operations, this pivotal role will serve as the on-site leader of the Equipment Engineering team, with a strong focus on team leadership, cross-functional collaboration, and operational excellence. As the Supervisor, this individual is responsible for managing and tracking equipment throughout the R&amp;D and CLIA laboratories in adherence to regulatory policy and the overall Asset Lifecycle Management Program, including high-tech instrumentation such as spectrophotometers, liquid handlers, analyzers, and next-gen sequencers. The ideal candidate will have extensive hands-on experience with liquid handling robots and a deep understanding of asset lifecycle management, including equipment maintenance strategies, documentation, and regulatory compliance &nbsp; Location: This is an onsite position based out of our South San Francisco location Responsibilities: Manage a team of equipment engineers and associates, ensuring efficient operation, maintenance, calibration, and appropriate documentation and regulatory compliance of all laboratory equipment located within South San Francisco headquarters. Collaborate with Manager of Equipment Engineering and Operations to build, guide, mentor, and otherwise lead a world-class team of Equipment Engineers. Collaborate with the Manager of Equipment Engineering and Operations in the identification, planning, and execution of long-term strategic initiatives aimed at enhancing equipment reliability, driving continuous improvement, and achieving operational cost savings across the organization. Work closely with Quality Assurance team members to ensure all equipment, equipment processes, and equipment documentation meet CLIA, CAP, IVD, and/or FDA regulations, maintaining up-to-date knowledge of regulatory changes and implementing necessary adjustments. Support and optimize the equipment lifecycle program from procurement, installation, qualification (IQ/OQ/PQ), calibration, maintenance, and decommissioning. Oversee the maintenance and calibration of all lab instrumentation in adherence to defined schedules. Coordinate equipment events (maintenance, calibration, onboarding, relocation, verifications, qualifications, decommission) across internal stakeholders (R&amp;D and CLIA) and external vendors to minimize impact on lab workflows while ensuring regulatory compliance. Manage relationships with external vendors and service providers to ensure timely support, quality service, and cost-effective solutions. Oversee the maintenance of accurate and detailed records of equipment maintenance, calibration, and repairs. Oversee the creation and management of all equipment documentation, including manuals, logs, and reports. Develop equipment specifications, user requirements, IQ/OQ protocols, preventive maintenance strategies, PM schedules. Provide mentorship and training both within and outside the Equipment Engineering and Operations team on the proper use and maintenance of lab equipment. Who You Are: &nbsp; 5+ years of related experience with BS/BA or higher degree in an Engineering field or equivalent work experience. 5+ years of experience in the clinical diagnostics industry, with a focus on equipment repair and equipment fleet management in clinical labs. 3+ years of experience developing/writing equipment user requirements, qualification plans, calibration/maintenance strategies, and maintenance &amp; operations procedures. 2+ years in a supervisory role. 1+ years of experience working with IT networking and systems infrastructure. Strong analytical and problem-solving skills with the ability to diagnose complex equipment issues and drive resolution independently or collaboratively. Proven ability to lead and manage a team, with strong organizational and communicational skills. Excellent attention to detail in record keeping and documentation. Preferred Qualifications Training in one or more major laboratory equipment platforms such as Hamilton Robotics, Unchained Labs, Tecan, Beckman, or Illumina. Familiarity with CMMS and LIMS integration. Working knowledge of root cause analysis tools (e.g. 5 whys, fishbone, FMEA) and reliability principles. Experience with Six Sigma principals or other reliability certification a significant plus. &nbsp; #LI-Onsite &nbsp;The final salary offered to a successful candidate will be dependent on several factors that may include but are not limited to the type and length of experience within the job, type and length of experience within the industry, education, etc. Base pay is one part of the Total Package that is provided to compensate and recognize employees for their work, and this role may be eligible for additional discretionary bonuses/incentives, and restricted stock units. Veracyte is a multi-state employer, and this salary range may not reflect positions that work in other states.Pay range$137,000&mdash;$149,000 USD&nbsp; What We Can Offer You Veracyte is a growing company that offers significant career opportunities if you are curious, driven, patient-oriented and aspire to help us build a great company. We offer competitive compensation and benefits, and are committed to fostering an inclusive workforce, where diverse backgrounds are represented, engaged, and empowered to drive innovative ideas and decisions. We are thrilled to be recognized as a 2024 Certified™ Great Place to Work® in both the US and Israel - a testament to our dynamic, inclusive, and inspiring workplace where passion meets purpose. &nbsp; About Veracyte Veracyte&nbsp;(Nasdaq: VCYT) is a global genomic diagnostics company that improves patient care by providing answers to clinical questions, informing diagnosis and treatment decisions throughout the patient journey in cancer and other diseases. The company’s growing menu of genomic tests leverage advances in genomic science and technology, enabling patients to avoid risky, costly diagnostic procedures and quicken time to appropriate treatment. The company’s tests in lung cancer, prostate cancer, breast cancer, thyroid cancer, bladder cancer and idiopathic pulmonary fibrosis are available to patients and its lymphoma subtyping and renal cancer tests are in development. With Veracyte’s exclusive global license to a best-in-class diagnostics instrument platform, the company is positioned to deliver its tests to patients worldwide.&nbsp;Veracyte&nbsp;is based in&nbsp;South San Francisco, California. For more information, please visit&nbsp;www.veracyte.com and follow the company on X (Formerly Twitter). Veracyte, Inc. is an Equal Opportunity Employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status or disability status. Veracyte participates in E-Verify in the United States. View our&nbsp;CCPA Disclosure Notice. If you receive any suspicious alerts or communications through LinkedIn or other online job sites for any position at Veracyte, please exercise caution and promptly report any concerns to careers@veracyte.com

Supervisor, Equipment Engineering and Operations

At Veracyte, we offer exciting career opportunities for those interested in joining a pioneering team that is committed to transforming cancer care for patients across the globe. Working at Veracyte enables our employees to not only make a meaningful impact on the lives of patients, but to also learn and grow within a purpose driven&nbsp;environment. This is what we call the Veracyte way&nbsp;– it’s about how we work together, guided by our values, to give clinicians the insights they need to help patients make life-changing decisions.&nbsp; Our Values: We Seek A Better Way: We innovate boldly, learn from our setbacks, and are resilient in our pursuit to transform cancer care We Make It Happen: We act with urgency, commit to quality, and bring fun to our hard work We Are Stronger Together:&nbsp;We collaborate openly, seek to understand, and celebrate our wins We Care Deeply: We embrace our differences, do the right thing, and encourage each other &nbsp;The Position: As a Talent Acquisition Coordinator at Veracyte, you will play a critical role in supporting our Talent Acquisition team to deliver a seamless and engaging candidate experience. You’ll be the operational backbone of our recruiting process, ensuring that every step—from opening a role to onboarding a new hire—is executed with precision, care, and a commitment to excellence. This role is ideal for someone who thrives in a fast-paced environment, enjoys building relationships, and is passionate about transforming cancer care through talent. This is a temporary assignment until the end of 2025.&nbsp; Responsibilities Requisition Management: Partner with recruiters and hiring managers to open new requisitions in Greenhouse, ensuring accurate and timely data entry. Interview Coordination: Coordinate and schedule candidate interviews across multiple time zones, maintaining clear communication with candidates and internal stakeholders. Background Checks: Follow up with candidates and third-party vendors to ensure timely completion of background checks. Offer Letters: Draft, manage the approval process and distribute offer letters in alignment with company policies and compensation guidelines. Onboarding Support: Prepare onboarding notices and collaborate with HR Shared Services to ensure a smooth Day 1 experience for candidates and hiring managers. Compliance &amp; Documentation: Create and maintain employee files in accordance with compliance and data privacy standards. Contingent Workforce Management: Manage contingent worker onboarding, tracking, and offboarding processes. Sourcing Support: Assist with sourcing candidates for open positions using AI, LinkedIn, job boards, and other sourcing tools. Reporting &amp; Analytics: Maintain recruiting dashboards and reports to track progress and identify areas for improvement. Design Greenhouse Reports for Talent Acquisition KPI’s and leadership. System Administration: Manage user access within Greenhouse, including adding new users and updating permissions as needed to ensure system integrity and compliance. Contracts Management: Enter and track workflow of contracts in the Ironclad approval system for routing and compliance Process Improvement: Proactively explore and implement advanced processes including but not limited to Greenhouse features—such as interview kits, automated workflows, and reporting dashboards—to streamline recruiting operations and enhance team efficiency. Candidate Experience: Support employer branding initiatives and candidate engagement efforts. Champion Veracyte’s values—We Care Deeply,&nbsp;We Make It Happen,&nbsp;We Seek a Better Way, and&nbsp;We Are Stronger Together—in every interaction. &nbsp; Who You Are: Required Qualifications 1–3 years of experience in recruiting coordination, HR operations, or a related administrative role. Strong organizational skills with the ability to manage multiple priorities and deadlines. Experience using an ATS (Greenhouse strongly preferred) and scheduling tools (Outlook, MS Teams, Excel, etc.). Excellent written and verbal communication skills. High attention to detail and commitment to data accuracy. Demonstrated ability to work collaboratively across teams and departments. A proactive mindset with a willingness to learn and adapt. Preferred Qualifications Experience in a biotech, life sciences, or healthcare environment preferred but not required. Familiarity with background check platforms and HRIS systems. Exposure to contingent workforce management. Basic sourcing experience using LinkedIn Recruiter or similar platforms. Understanding of compliance and confidentiality in HR practices. #LI-Remote, #LI-Hybrid &nbsp;The final salary offered to a successful candidate will be dependent on several factors that may include but are not limited to the type and length of experience within the job, type and length of experience within the industry, education, etc. Base pay is one part of the Total Package that is provided to compensate and recognize employees for their work, and this role may be eligible for additional discretionary bonuses/incentives, and restricted stock units. Veracyte is a multi-state employer, and this salary range may not reflect positions that work in other states.Pay range$28&mdash;$35 USD&nbsp; What We Can Offer You Veracyte is a growing company that offers significant career opportunities if you are curious, driven, patient-oriented and aspire to help us build a great company. We offer competitive compensation and benefits, and are committed to fostering an inclusive workforce, where diverse backgrounds are represented, engaged, and empowered to drive innovative ideas and decisions. We are thrilled to be recognized as a 2024 Certified™ Great Place to Work® in both the US and Israel - a testament to our dynamic, inclusive, and inspiring workplace where passion meets purpose. &nbsp; About Veracyte Veracyte&nbsp;(Nasdaq: VCYT) is a global genomic diagnostics company that improves patient care by providing answers to clinical questions, informing diagnosis and treatment decisions throughout the patient journey in cancer and other diseases. The company’s growing menu of genomic tests leverage advances in genomic science and technology, enabling patients to avoid risky, costly diagnostic procedures and quicken time to appropriate treatment. The company’s tests in lung cancer, prostate cancer, breast cancer, thyroid cancer, bladder cancer and idiopathic pulmonary fibrosis are available to patients and its lymphoma subtyping and renal cancer tests are in development. With Veracyte’s exclusive global license to a best-in-class diagnostics instrument platform, the company is positioned to deliver its tests to patients worldwide.&nbsp;Veracyte&nbsp;is based in&nbsp;South San Francisco, California. For more information, please visit&nbsp;www.veracyte.com and follow the company on X (Formerly Twitter). Veracyte, Inc. is an Equal Opportunity Employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status or disability status. Veracyte participates in E-Verify in the United States. View our&nbsp;CCPA Disclosure Notice. If you receive any suspicious alerts or communications through LinkedIn or other online job sites for any position at Veracyte, please exercise caution and promptly report any concerns to careers@veracyte.com

Talent Acquisition Coordinator - Temporary

At Veracyte, we offer exciting career opportunities for those interested in joining a pioneering team that is committed to transforming cancer care for patients across the globe. Working at Veracyte enables our employees to not only make a meaningful impact on the lives of patients, but to also learn and grow within a purpose driven&nbsp;environment. This is what we call the Veracyte way&nbsp;– it’s about how we work together, guided by our values, to give clinicians the insights they need to help patients make life-changing decisions.&nbsp; Our Values: We Seek A Better Way: We innovate boldly, learn from our setbacks, and are resilient in our pursuit to transform cancer care We Make It Happen: We act with urgency, commit to quality, and bring fun to our hard work We Are Stronger Together:&nbsp;We collaborate openly, seek to understand, and celebrate our wins We Care Deeply: We embrace our differences, do the right thing, and encourage each other &nbsp;The Position: The Technical Product Manager (TPM) on the Veracyte Data Engineering team will lead the product strategy, development, and lifecycle management of data engineering solutions, including the Veracyte Lakehouse and related data cataloging initiatives. This role bridges technical and business needs, collaborating with data engineers, data scientists, and cross-functional teams in a Scrum environment to deliver scalable, secure, and innovative data products aligned with Veracyte’s global data strategy and digital transformation goals. This position is based out of our San Diego office (hybrid) and we are open to remote (US, PST ideal). Key Responsibilities: Define and Execute Product Vision: Develop and maintain the product roadmap and backlog for data engineering solutions, prioritizing features based on business value, user needs, and technical feasibility. Serve as the Scrum Product Owner, managing the team’s unified backlog and ensuring alignment with organizational objectives. Collaborate Across Teams: Work with data engineers, data scientists, and stakeholders to gather requirements, translate them into user stories, and oversee their implementation via Jira. Facilitate backlog grooming, sprint planning, and daily stand-up meetings to drive team progress. Conduct Research and Analysis: Perform market and competitive analysis to identify opportunities for enhancing data infrastructure, pipelines, and cataloging tools. Gather user feedback to refine data products and ensure they meet the needs of technical and non-technical audiences. Oversee Data Management and Governance: Ensure data engineering solutions comply with data governance policies, security standards, and regulatory requirements. Support the design and implementation of a data catalog framework, leveraging tools and best practices for data source discovery and accessibility. Drive Data Strategy and Innovation: Collaborate with leadership to align data engineering initiatives with Veracyte’s overall data and digital strategies. Recommend best practices for scalability, security, and usability in data products, including integration with AWS, Snowflake, and open formats like Apache Parquet. Provide training and documentation for internal teams and stakeholders on data engineering tools and processes. Mentorship and Collaboration: Mentor junior product team members and foster cross-disciplinary collaboration to promote innovation and continuous improvement. Act as a liaison between technical teams and business units to ensure successful product delivery. Who You Are: Education: Bachelor’s or Master’s degree in Computer Science, Engineering, Data Science, or a related field. Experience: 5+ years of experience in product management, with a focus on technical products in data engineering, cloud services, or software development. Experience working in a Scrum environment as a Product Owner is highly desirable. Technical Skills: Familiarity with data engineering concepts, including data lakes, pipelines, and cataloging tools. Understanding of cloud platforms (e.g., AWS, GCP) and data warehousing solutions (e.g., Snowflake). Basic knowledge of programming languages (e.g., Python, SQL) and data modeling is a plus. Soft Skills: Strong analytical and problem-solving skills. Excellent communication skills to convey technical concepts to diverse audiences. Proven ability to manage cross-functional projects in a fast-paced, innovative environment. &nbsp; #LI-Hybrid, or #LI-Remote &nbsp;The final salary offered to a successful candidate will be dependent on several factors that may include but are not limited to the type and length of experience within the job, type and length of experience within the industry, education, etc. Base pay is one part of the Total Package that is provided to compensate and recognize employees for their work, and this role may be eligible for additional discretionary bonuses/incentives, and restricted stock units. Veracyte is a multi-state employer, and this salary range may not reflect positions that work in other states.Pay range$118,000&mdash;$144,000 USD&nbsp; What We Can Offer You Veracyte is a growing company that offers significant career opportunities if you are curious, driven, patient-oriented and aspire to help us build a great company. We offer competitive compensation and benefits, and are committed to fostering an inclusive workforce, where diverse backgrounds are represented, engaged, and empowered to drive innovative ideas and decisions. We are thrilled to be recognized as a 2024 Certified™ Great Place to Work® in both the US and Israel - a testament to our dynamic, inclusive, and inspiring workplace where passion meets purpose. &nbsp; About Veracyte Veracyte&nbsp;(Nasdaq: VCYT) is a global genomic diagnostics company that improves patient care by providing answers to clinical questions, informing diagnosis and treatment decisions throughout the patient journey in cancer and other diseases. The company’s growing menu of genomic tests leverage advances in genomic science and technology, enabling patients to avoid risky, costly diagnostic procedures and quicken time to appropriate treatment. The company’s tests in lung cancer, prostate cancer, breast cancer, thyroid cancer, bladder cancer and idiopathic pulmonary fibrosis are available to patients and its lymphoma subtyping and renal cancer tests are in development. With Veracyte’s exclusive global license to a best-in-class diagnostics instrument platform, the company is positioned to deliver its tests to patients worldwide.&nbsp;Veracyte&nbsp;is based in&nbsp;South San Francisco, California. For more information, please visit&nbsp;www.veracyte.com and follow the company on X (Formerly Twitter). Veracyte, Inc. is an Equal Opportunity Employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status or disability status. Veracyte participates in E-Verify in the United States. View our&nbsp;CCPA Disclosure Notice. If you receive any suspicious alerts or communications through LinkedIn or other online job sites for any position at Veracyte, please exercise caution and promptly report any concerns to careers@veracyte.com

Technical Product Manager

At Veracyte, we offer exciting career opportunities for those interested in joining a pioneering team that is committed to transforming cancer care for patients across the globe. Working at Veracyte enables our employees to not only make a meaningful impact on the lives of patients, but to also learn and grow within a purpose driven&nbsp;environment. This is what we call the Veracyte way&nbsp;– it’s about how we work together, guided by our values, to give clinicians the insights they need to help patients make life-changing decisions.&nbsp; Our Values: We Seek A Better Way: We innovate boldly, learn from our setbacks, and are resilient in our pursuit to transform cancer care We Make It Happen: We act with urgency, commit to quality, and bring fun to our hard work We Are Stronger Together:&nbsp;We collaborate openly, seek to understand, and celebrate our wins We Care Deeply: We embrace our differences, do the right thing, and encourage each other &nbsp;The Position: We are seeking a detail-oriented and highly collaborative Technical Writer to support the PMO team in documenting processes, frameworks, and project deliverables across Veracyte’s product development process lifecycle. This role will be instrumental in translating complex technical and operational concepts into clear, accessible documentation that supports cross-functional alignment and regulatory compliance. *Please note this is a temporary 3 month position with potential extension* This is a hybrid position based in our San Diego, CA office. Based on candidate location, we may consider (PST) remote. Monday-Friday, 8AM-5PM. Key Responsibilities:&nbsp;&nbsp; Collaborate with PMO leaders, Core Team Leads, and subject matter experts to document product development processes (PDP), project governance models, and stage gate frameworks&nbsp; Write user-friendly content that meets the needs of target audience, turning insights into language for user success&nbsp; Create templates, SOPs, and technical documentation that support PMO operations, including PDP, resource management, and project tracking&nbsp; Ensure consistency in style, tone, and formatting across all PMO documentation, adhering to Veracyte’s internal standards and branding guidelines&nbsp; Other duties as assigned&nbsp; Location: This is a hybrid/onsite position based in our San Diego, CA location. Based on candidate location, we may consider (PST) remote. Who You Are: Minimum of 7 years of proven experience in technical writing within biotech, diagnostics, or healthcare industries.&nbsp; Experience with product development processes, regulatory documentation, and project management methodologies.&nbsp; Proven ability to quickly learn and understand complex subject matter&nbsp; Excellent written and verbal communication skills with a keen eye for detail.&nbsp; Ability to work independently and collaboratively in a fast-paced, matrixed environment. High School degree or equivalent degree required. #LI-Hybrid &nbsp;The final salary offered to a successful candidate will be dependent on several factors that may include but are not limited to the type and length of experience within the job, type and length of experience within the industry, education, etc. Base pay is one part of the Total Package that is provided to compensate and recognize employees for their work, and this role may be eligible for additional discretionary bonuses/incentives, and restricted stock units. Veracyte is a multi-state employer, and this salary range may not reflect positions that work in other states.Pay range$56&mdash;$63 USD&nbsp; What We Can Offer You Veracyte is a growing company that offers significant career opportunities if you are curious, driven, patient-oriented and aspire to help us build a great company. We offer competitive compensation and benefits, and are committed to fostering an inclusive workforce, where diverse backgrounds are represented, engaged, and empowered to drive innovative ideas and decisions. We are thrilled to be recognized as a 2024 Certified™ Great Place to Work® in both the US and Israel - a testament to our dynamic, inclusive, and inspiring workplace where passion meets purpose. &nbsp; About Veracyte Veracyte&nbsp;(Nasdaq: VCYT) is a global genomic diagnostics company that improves patient care by providing answers to clinical questions, informing diagnosis and treatment decisions throughout the patient journey in cancer and other diseases. The company’s growing menu of genomic tests leverage advances in genomic science and technology, enabling patients to avoid risky, costly diagnostic procedures and quicken time to appropriate treatment. The company’s tests in lung cancer, prostate cancer, breast cancer, thyroid cancer, bladder cancer and idiopathic pulmonary fibrosis are available to patients and its lymphoma subtyping and renal cancer tests are in development. With Veracyte’s exclusive global license to a best-in-class diagnostics instrument platform, the company is positioned to deliver its tests to patients worldwide.&nbsp;Veracyte&nbsp;is based in&nbsp;South San Francisco, California. For more information, please visit&nbsp;www.veracyte.com and follow the company on X (Formerly Twitter). Veracyte, Inc. is an Equal Opportunity Employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status or disability status. Veracyte participates in E-Verify in the United States. View our&nbsp;CCPA Disclosure Notice. If you receive any suspicious alerts or communications through LinkedIn or other online job sites for any position at Veracyte, please exercise caution and promptly report any concerns to careers@veracyte.com

Technical Writer - Temporary

At Veracyte, we offer exciting career opportunities for those interested in joining a pioneering team that is committed to transforming cancer care for patients across the globe. Working at Veracyte enables our employees to not only make a meaningful impact on the lives of patients, but to also learn and grow within a purpose driven&nbsp;environment. This is what we call the Veracyte way&nbsp;– it’s about how we work together, guided by our values, to give clinicians the insights they need to help patients make life-changing decisions.&nbsp; Our Values: We Seek A Better Way: We innovate boldly, learn from our setbacks, and are resilient in our pursuit to transform cancer care We Make It Happen: We act with urgency, commit to quality, and bring fun to our hard work We Are Stronger Together:&nbsp;We collaborate openly, seek to understand, and celebrate our wins We Care Deeply: We embrace our differences, do the right thing, and encourage each other &nbsp;The Position: The TPRM Manager will be responsible for leading the company’s Third-Party Risk Management program, evaluating and mitigating risks associated with security, artificial intelligence (AI) systems and data privacy. You will ensure that vendors, suppliers, and partners meet our security, compliance, and operational standards due diligence. You will work closely with IT Security, Legal, Privacy, Procurement, and Business Units to assess risks, drive remediation, and maintain compliance with regulatory requirements (SOC 2, ISO 27001, HIPAA, HITRUST, etc.). The ideal candidate is an experienced, detailed-oriented, and strategic in assessing information technology and security risks. Key Responsibilities: Program Ownership Lead the design, implementation, and continuous improvement of the Third-Party Risk Management program. Develop and deploy methods to better identify emerging risks associated with third party vendors Establish TPRM governance policies, standards, and procedures for vendor risk assessment and ongoing monitoring. Drive continuous improvement of the process and lead designing and facilitating tools to streamline TPRM Collaborate and build strong relationships with all key business unit stakeholders to educate on the program and offer advice on security vendor risk mitigation as needed. Perform as a subject matter expert on TPRM with responsibilities to review and assess all vendors onboarding in the organization. Train enterprise wide on TPRM process to ensure compliance with regulatory requirements Contribute to establishing an enterprise risk committee Vendor Risk Assessments Conduct due diligence and risk assessments on new and existing third-party vendors. Evaluate vendor’s security and AI controls, compliance certifications, and contractual obligations. Collaborate with business owners to ensure vendors meet security, AI, privacy, and operational requirements. Monitoring &amp; Reporting Develop and maintain a vendor risk register and reassess vendors based on risk profile Monitor critical vendors for emerging risks, changes in risk posture, and compliance gaps. Provide dashboards, metrics, and executive reporting to leadership and audit committees. Cross-Functional Collaboration Partner with IT Security, Procurement, Legal, Privacy and Business Units to integrate TPRM into onboarding and procurement workflows. Support internal and external audits with vendor risk management evidence. Remediation &amp; Continuous Improvement Track remediation activities for vendors with identified risks or findings. Lead initiatives to streamline vendor assessments, automate workflows, and integrate with GRC platforms. Stay current with emerging risks trends (ie AI, Cyber), regulatory updates and best practices. Who You Are: Bachelor’s degree in Information Security, Business Administration, Risk Management, or related field. 8+ years of experience in Third Party Vendor Risk Management, IT, AI and Cybersecurity risks, or GRC program management. Familiarity with risk and compliance frameworks (NIST, SOC 2, ISO 27001, HIPAA, HITRUST). Experience with TPRM or GRC platforms (e.g., Archer, OneTrust, ServiceNow GRC, ProcessUnity). Strong analytical and communication skills; ability to influence stakeholders across functions. Experience presenting risk findings and metrics to executives or audit committees. A subject matter expert to identify and address key third party related risks and areas of concerns associated with new and existing third-party vendors Knowledge of assessing vendors’ AI risks Preferred Skills: Industry certifications: CTPRP (Certified Third-Party Risk Professional),Certified Regulatory Vendor Program Manager (CRVPM) CISA, CISM, CISSP, CRISC, or similar. Experience in regulated industries such as healthcare, biotech, or financial services. Knowledge of contract negotiation, vendor SLAs, and regulatory obligations. #LI-Remote &nbsp;The final salary offered to a successful candidate will be dependent on several factors that may include but are not limited to the type and length of experience within the job, type and length of experience within the industry, education, etc. Base pay is one part of the Total Package that is provided to compensate and recognize employees for their work, and this role may be eligible for additional discretionary bonuses/incentives, and restricted stock units. Veracyte is a multi-state employer, and this salary range may not reflect positions that work in other states.Pay range$165,000&mdash;$180,000 USD&nbsp; What We Can Offer You Veracyte is a growing company that offers significant career opportunities if you are curious, driven, patient-oriented and aspire to help us build a great company. We offer competitive compensation and benefits, and are committed to fostering an inclusive workforce, where diverse backgrounds are represented, engaged, and empowered to drive innovative ideas and decisions. We are thrilled to be recognized as a 2024 Certified™ Great Place to Work® in both the US and Israel - a testament to our dynamic, inclusive, and inspiring workplace where passion meets purpose. &nbsp; About Veracyte Veracyte&nbsp;(Nasdaq: VCYT) is a global genomic diagnostics company that improves patient care by providing answers to clinical questions, informing diagnosis and treatment decisions throughout the patient journey in cancer and other diseases. The company’s growing menu of genomic tests leverage advances in genomic science and technology, enabling patients to avoid risky, costly diagnostic procedures and quicken time to appropriate treatment. The company’s tests in lung cancer, prostate cancer, breast cancer, thyroid cancer, bladder cancer and idiopathic pulmonary fibrosis are available to patients and its lymphoma subtyping and renal cancer tests are in development. With Veracyte’s exclusive global license to a best-in-class diagnostics instrument platform, the company is positioned to deliver its tests to patients worldwide.&nbsp;Veracyte&nbsp;is based in&nbsp;South San Francisco, California. For more information, please visit&nbsp;www.veracyte.com and follow the company on X (Formerly Twitter). Veracyte, Inc. is an Equal Opportunity Employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status or disability status. Veracyte participates in E-Verify in the United States. View our&nbsp;CCPA Disclosure Notice. If you receive any suspicious alerts or communications through LinkedIn or other online job sites for any position at Veracyte, please exercise caution and promptly report any concerns to careers@veracyte.com

Third-Party Risk Management Manager

At Veracyte, we offer exciting career opportunities for those interested in joining a pioneering team that is committed to transforming cancer care for patients across the globe. Working at Veracyte enables our employees to not only make a meaningful impact on the lives of patients, but to also learn and grow within a purpose driven&nbsp;environment. This is what we call the Veracyte way&nbsp;– it’s about how we work together, guided by our values, to give clinicians the insights they need to help patients make life-changing decisions.&nbsp; Our Values: We Seek A Better Way: We innovate boldly, learn from our setbacks, and are resilient in our pursuit to transform cancer care We Make It Happen: We act with urgency, commit to quality, and bring fun to our hard work We Are Stronger Together:&nbsp;We collaborate openly, seek to understand, and celebrate our wins We Care Deeply: We embrace our differences, do the right thing, and encourage each other &nbsp;The Position We are seeking an exceptional Vice President of Sales or National Sales Executive Director to lead our commercial breast oncology organization while also shaping the future of diagnostic medicine. The successful candidate will be an analytical, inspiring and data-driven leader who exceeds sales goals by developing and executing clear sales strategies. The primary goal of this role is to successfully launch and establish the Prosigna Breast Cancer Assay as a first-in-class Laboratory Developed Test in the United States. The Prosigna Breast Cancer Assay is a prognostic test that helps inform treatment decisions for patients with early-stage breast cancer. Leading, building and developing the sales organization: This includes recruiting, hiring, training and mentoring a team of sales professionals and account executives. Strategic Planning and Execution: Developing and implementing comprehensive business plans and sales strategies to drive adoption of the Prosigna Breast Cancer Assay (LDT) and achieve revenue/growth targets. Coordinate with MSL and Marketing teams to develop HCP education and marketing tools, assets. Relationship Management: Developing, building and maintaining strong relationships with Key Opinion Leaders (KOLs), large accounts and other stakeholders to gain insights and influence sales direction Cross-Functional Collaboration: Partnering across the organization with marketing, medical affairs, managed care, customer service, billing to bring our physicians the best possible product and customer experience Performance Management: Monitoring sales performance, providing coaching and feedback to sales professionals to achieve business objectives, reporting results and plans to company leadership Compliance and Quality: Ensuring the sales team is compliant with all Veracyte policies, procedures, and regulatory requirements Who You Are: Successful candidates will have experience in launching diagnostic tests, developing sales strategy, coaching sales leaders, performance management, evaluating sales metrics, channel development, and strong verbal, written and presentation communication skills.&nbsp;&nbsp; Success in this role demands a deep understanding of the breast oncology space, strong clinical acumen, and the ability to navigate complex healthcare systems while fostering trusted, value-driven relationships with physicians. You must have extensive experience in recruiting and hiring top talent. You have at least 15 years of related experience in a fast paced, results-oriented, rapidly growing company in diagnostics, life sciences, or medical technology.&nbsp; In addition, you have at least 10-years of previous sales leadership experience in healthcare; preferably diagnostics or medical devices. The ability to travel up to 50% is required.&nbsp; #LI-Onsite, #LI-Hybrid, or #LI-Remote &nbsp;The final salary offered to a successful candidate will be dependent on several factors that may include but are not limited to the type and length of experience within the job, type and length of experience within the industry, education, etc. Base pay is one part of the Total Package that is provided to compensate and recognize employees for their work, and this role may be eligible for additional discretionary bonuses/incentives, and restricted stock units. Veracyte is a multi-state employer, and this salary range may not reflect positions that work in other states.Pay range$234,500&mdash;$270,000 USD&nbsp; What We Can Offer You Veracyte is a growing company that offers significant career opportunities if you are curious, driven, patient-oriented and aspire to help us build a great company. We offer competitive compensation and benefits, and are committed to fostering an inclusive workforce, where diverse backgrounds are represented, engaged, and empowered to drive innovative ideas and decisions. We are thrilled to be recognized as a 2024 Certified™ Great Place to Work® in both the US and Israel - a testament to our dynamic, inclusive, and inspiring workplace where passion meets purpose. &nbsp; About Veracyte Veracyte&nbsp;(Nasdaq: VCYT) is a global genomic diagnostics company that improves patient care by providing answers to clinical questions, informing diagnosis and treatment decisions throughout the patient journey in cancer and other diseases. The company’s growing menu of genomic tests leverage advances in genomic science and technology, enabling patients to avoid risky, costly diagnostic procedures and quicken time to appropriate treatment. The company’s tests in lung cancer, prostate cancer, breast cancer, thyroid cancer, bladder cancer and idiopathic pulmonary fibrosis are available to patients and its lymphoma subtyping and renal cancer tests are in development. With Veracyte’s exclusive global license to a best-in-class diagnostics instrument platform, the company is positioned to deliver its tests to patients worldwide.&nbsp;Veracyte&nbsp;is based in&nbsp;South San Francisco, California. For more information, please visit&nbsp;www.veracyte.com and follow the company on X (Formerly Twitter). Veracyte, Inc. is an Equal Opportunity Employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status or disability status. Veracyte participates in E-Verify in the United States. View our&nbsp;CCPA Disclosure Notice. If you receive any suspicious alerts or communications through LinkedIn or other online job sites for any position at Veracyte, please exercise caution and promptly report any concerns to careers@veracyte.com

VP Sales - Breast

At Veracyte, we offer exciting career opportunities for those interested in joining a pioneering team that is committed to transforming cancer care for patients across the globe. Working at Veracyte enables our employees to not only make a meaningful impact on the lives of patients, but to also learn and grow within a purpose driven&nbsp;environment. This is what we call the Veracyte way&nbsp;– it’s about how we work together, guided by our values, to give clinicians the insights they need to help patients make life-changing decisions.&nbsp; Our Values: We Seek A Better Way: We innovate boldly, learn from our setbacks, and are resilient in our pursuit to transform cancer care We Make It Happen: We act with urgency, commit to quality, and bring fun to our hard work We Are Stronger Together:&nbsp;We collaborate openly, seek to understand, and celebrate our wins We Care Deeply: We embrace our differences, do the right thing, and encourage each other &nbsp;The Position: Veracyte is seeking an innovative and motivated Biostatistician to join our dynamic and industry-leading data analysis team, focusing on internal and external collaborations to demonstrate the validity and utility of our biomarker signatures and diagnostic tests. This individual will collaborate closely with internal and external experts to jointly interrogate genomic and clinical data and provide sound strategic, scientific, and statistical input to support the biomarker signatures / diagnostic tests evaluation and improve patient care. This person will perform rigorous and thorough analyses following best practices to propel the wide adoption of our biomarker signatures /diagnostic tests.&nbsp; Veracyte prides itself on its collaborative and fast-paced environment, offering employees room to learn and grow across functions. In this role, the individual will gain valuable knowledge and experience while working for a company that is charting new territory in the molecular diagnostics industry in its efforts to bring to market a portfolio of high-value advanced molecular diagnostics on a distributed platform globally. This is a high-impact role in which the successful candidate will see the fruits of their efforts implemented rapidly in the clinic and will be pivotal in advancing Veracyte’s vision of improving outcomes for patients all over the world at every step of their journey.&nbsp; Location: This is a hybrid position based in our San Diego office. Based on candidate location, we may consider (PST) remote. Responsibilities:&nbsp; Independently or under limited supervision, provide sound strategic, scientific, and statistical input to support the company’s biomarker discovery and validation work Provide statistical expertise to various other teams within the company including Medical Affairs, Clinical Operation, Sales and Marketing, Lab Operations, and Regulatory Affairs Lead statistical analyses for the company’s clinical evidence generation efforts, including the drafting and execution of statistical analysis plans and presentation of statistical results to both internal and external collaborators Author the statistical section of study protocols and grant applications, incorporating appropriate statistical methods for study design and analysis. Author statistical analysis plans for clinical studies when appropriate and lead study design efforts. Author the method and result sections of scientific manuscripts Take responsibility for the scientific integrity of clinical studies and the accuracy of the reported results Engage and lead discussions and research to improve statistical methodologies Represent the company as a biostatistics expert at professional conferences Who You Are: PhD in statistics, biostatistics, or related statistical program with a minimum of 3 years of related experience including a strong publication record in high impact peer-reviewed journals. Expert knowledge of theoretical and applied statistics is required, with an emphasis on methods appropriate for prospective and retrospective studies related to biomedical and public health sciences including survival analysis. Strong analytical skills and demonstrated expertise in programming: experience with R statistical software language is required, including data visualization packages Excellent interpersonal, oral, and written communication skills are required, including the ability to explain nuanced or complicated results to non-subject area experts and able to create compelling and digestible visualizations to support analysis conclusions. Passionate about the intersection of statistics and medical science and its potential applications in the diagnostics space and deep commitment to improving patient lives. Preferred skills:&nbsp; Experience with an array platform, NGS, or high-throughput technology. Familiarity with clinical trials and knowledge in epidemiology. Knowledge of FDA, CLIA or other regulatory guidelines. Familiarity with biomarker research. #LI-Hybrid &nbsp;The final salary offered to a successful candidate will be dependent on several factors that may include but are not limited to the type and length of experience within the job, type and length of experience within the industry, education, etc. Base pay is one part of the Total Package that is provided to compensate and recognize employees for their work, and this role may be eligible for additional discretionary bonuses/incentives, and restricted stock units. Veracyte is a multi-state employer, and this salary range may not reflect positions that work in other states.Pay range$130,000&mdash;$145,000 USD&nbsp; What We Can Offer You Veracyte is a growing company that offers significant career opportunities if you are curious, driven, patient-oriented and aspire to help us build a great company. We offer competitive compensation and benefits, and are committed to fostering an inclusive workforce, where diverse backgrounds are represented, engaged, and empowered to drive innovative ideas and decisions. We are thrilled to be recognized as a 2024 Certified™ Great Place to Work® in both the US and Israel - a testament to our dynamic, inclusive, and inspiring workplace where passion meets purpose. &nbsp; About Veracyte Veracyte&nbsp;(Nasdaq: VCYT) is a global genomic diagnostics company that improves patient care by providing answers to clinical questions, informing diagnosis and treatment decisions throughout the patient journey in cancer and other diseases. The company’s growing menu of genomic tests leverage advances in genomic science and technology, enabling patients to avoid risky, costly diagnostic procedures and quicken time to appropriate treatment. The company’s tests in lung cancer, prostate cancer, breast cancer, thyroid cancer, bladder cancer and idiopathic pulmonary fibrosis are available to patients and its lymphoma subtyping and renal cancer tests are in development. With Veracyte’s exclusive global license to a best-in-class diagnostics instrument platform, the company is positioned to deliver its tests to patients worldwide.&nbsp;Veracyte&nbsp;is based in&nbsp;South San Francisco, California. For more information, please visit&nbsp;www.veracyte.com and follow the company on X (Formerly Twitter). Veracyte, Inc. is an Equal Opportunity Employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status or disability status. Veracyte participates in E-Verify in the United States. View our&nbsp;CCPA Disclosure Notice. If you receive any suspicious alerts or communications through LinkedIn or other online job sites for any position at Veracyte, please exercise caution and promptly report any concerns to careers@veracyte.com

Biostatistician II

At Veracyte, we offer exciting career opportunities for those interested in joining a pioneering team that is committed to transforming cancer care for patients across the globe. Working at Veracyte enables our employees to not only make a meaningful impact on the lives of patients, but to also learn and grow within a purpose driven&nbsp;environment. This is what we call the Veracyte way&nbsp;– it’s about how we work together, guided by our values, to give clinicians the insights they need to help patients make life-changing decisions.&nbsp; Our Values: We Seek A Better Way: We innovate boldly, learn from our setbacks, and are resilient in our pursuit to transform cancer care We Make It Happen: We act with urgency, commit to quality, and bring fun to our hard work We Are Stronger Together:&nbsp;We collaborate openly, seek to understand, and celebrate our wins We Care Deeply: We embrace our differences, do the right thing, and encourage each other &nbsp;Location:&nbsp;This is a onsite position based in our San Diego,&nbsp;CA office.&nbsp; The schedule is Sunday - Thursday, 5am - 1:30pm. This shift is eligible for differential pay. This is a ONE- YEAR contract position.&nbsp; The Position:&nbsp; The Clinical Laboratory Scientist (CLS) is responsible for performing high complexity clinical laboratory testing on patient specimens, reviewing and reporting patient results, performing quality control and quality assurance activities, and complying with all applicable local, state and federal laboratory, quality, and safety requirements. The high complexity nature of the work requires excellent attention to detail, effective written and verbal communication skills, the ability to multitask and be flexible with tasks and&nbsp;schedules, and the ability to work independently and effectively in a team environment.&nbsp; ESSENTIAL DUTIES AND RESPONSIBILITIES:&nbsp; The main duties and responsibilities of the Clinical Laboratory Scientist include the following, but not limited to:&nbsp;• Perform molecular genetic testing on clinical specimens&nbsp;• Follow the laboratory's standard operating procedures for specimen handling, processing, test analyses, and recording of test results&nbsp;• Perform, review and document laboratory quality control procedures in accordance with the Quality Assurance Program&nbsp;• Complete assigned laboratory and non-laboratory tasks&nbsp;• Prepare reagents required for laboratory testing&nbsp;• Engage in training&nbsp;• Perform proficiency testing for the clinical tests&nbsp;• Assist in research and validation activities&nbsp;• Independently identify and troubleshoot basic issues that could potentially adversely affect test performance&nbsp;• Document all corrective actions taken when test systems deviate from the laboratory's established performance specifications&nbsp;• Follow the laboratory’s standard operating procedures for quality and environmental health and safety and report all concerns of test quality and/or safety to the Lab Supervisor or Safety Officer&nbsp;• Ensure all work is performed in accordance with local, state, and federal regulations and participate in all regulatory inspections&nbsp;• Work cooperatively in a team environment support fellow laboratory and management staff&nbsp;• Perform any other site/lab specific duties as assigned&nbsp; Who You Are:&nbsp; To perform this job successfully, an individual must be able to perform each essential duty satisfactorily.&nbsp;The requirements listed below are representative of the knowledge, skills, and/or abilities required. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions.&nbsp; EDUCATION and/or EXPERIENCE&nbsp;• Active California Department of Public Health Clinical Laboratory Scientist (CLS) license or Clinical Genetic Molecular Biology Scientist (CGMBS) license (no exceptions)&nbsp;• Must have strong analytical and problem-solving skills&nbsp;• Must be detail-oriented and comfortable with technology&nbsp;• Must have excellent verbal and written communication skills&nbsp;• Experience in high complexity clinical laboratory testing, preferably in molecular diagnostics&nbsp;• Performance of molecular testing (PCR, Microarray, Sanger/NGS sequencing) a plus&nbsp;• Strong computer skills across diverse platforms&nbsp;• Excellent interpersonal communication and team player attitude&nbsp;• Ability to adapt to change and a rapid work pace&nbsp;• Maintains continuing education units required by California Department of Health Services and New York State Department of Health.&nbsp; PHYSICAL REQUIREMENTS&nbsp;• Repetitive movement of hands, arms and leg, fingers (typing and/or writing)&nbsp;• Gripping/grasping&nbsp;• Reaching above/below shoulder level&nbsp;• Sitting, with occasional walking, standing, stooping and moving about&nbsp;• Exposure to general office environment conditions&nbsp;• Occasionally required to lift up to 25 pounds&nbsp; &nbsp; #LI-Onsite &nbsp;The final salary offered to a successful candidate will be dependent on several factors that may include but are not limited to the type and length of experience within the job, type and length of experience within the industry, education, etc. Base pay is one part of the Total Package that is provided to compensate and recognize employees for their work, and this role may be eligible for additional discretionary bonuses/incentives, and restricted stock units. Veracyte is a multi-state employer, and this salary range may not reflect positions that work in other states.Pay range$36&mdash;$50 USD&nbsp; What We Can Offer You Veracyte is a growing company that offers significant career opportunities if you are curious, driven, patient-oriented and aspire to help us build a great company. We offer competitive compensation and benefits, and are committed to fostering an inclusive workforce, where diverse backgrounds are represented, engaged, and empowered to drive innovative ideas and decisions. We are thrilled to be recognized as a 2024 Certified™ Great Place to Work® in both the US and Israel - a testament to our dynamic, inclusive, and inspiring workplace where passion meets purpose. &nbsp; About Veracyte Veracyte&nbsp;(Nasdaq: VCYT) is a global genomic diagnostics company that improves patient care by providing answers to clinical questions, informing diagnosis and treatment decisions throughout the patient journey in cancer and other diseases. The company’s growing menu of genomic tests leverage advances in genomic science and technology, enabling patients to avoid risky, costly diagnostic procedures and quicken time to appropriate treatment. The company’s tests in lung cancer, prostate cancer, breast cancer, thyroid cancer, bladder cancer and idiopathic pulmonary fibrosis are available to patients and its lymphoma subtyping and renal cancer tests are in development. With Veracyte’s exclusive global license to a best-in-class diagnostics instrument platform, the company is positioned to deliver its tests to patients worldwide.&nbsp;Veracyte&nbsp;is based in&nbsp;South San Francisco, California. For more information, please visit&nbsp;www.veracyte.com and follow the company on X (Formerly Twitter). Veracyte, Inc. is an Equal Opportunity Employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status or disability status. Veracyte participates in E-Verify in the United States. View our&nbsp;CCPA Disclosure Notice. If you receive any suspicious alerts or communications through LinkedIn or other online job sites for any position at Veracyte, please exercise caution and promptly report any concerns to careers@veracyte.com

Clinical Laboratory Scientist

At Veracyte, we offer exciting career opportunities for those interested in joining a pioneering team that is committed to transforming cancer care for patients across the globe. Working at Veracyte enables our employees to not only make a meaningful impact on the lives of patients, but to also learn and grow within a purpose driven&nbsp;environment. This is what we call the Veracyte way&nbsp;– it’s about how we work together, guided by our values, to give clinicians the insights they need to help patients make life-changing decisions.&nbsp; Our Values: We Seek A Better Way: We innovate boldly, learn from our setbacks, and are resilient in our pursuit to transform cancer care We Make It Happen: We act with urgency, commit to quality, and bring fun to our hard work We Are Stronger Together:&nbsp;We collaborate openly, seek to understand, and celebrate our wins We Care Deeply: We embrace our differences, do the right thing, and encourage each other &nbsp;The Position: The Lead Clinical Laboratory Scientist is responsible for performing high complexity clinical laboratory testing on patient specimens, reviewing and reporting patient results, performing quality control and quality assurance activities and complying with all applicable local, state and federal laboratory, quality, and safety requirements. The high complexity nature of the work requires excellent attention to detail, effective written and verbal communication skills, and the ability to multitask and be flexible with tasks and schedules and the ability to work independently and effectively in a team environment. This is an on-site position in our San Diego, CA lab. Sunday - Thursday 12:30pm - 9:00pm Essential Duties &amp; Responsibilities&nbsp; The main duties and responsibilities of the Lead Clinical Laboratory Scientist include the following, but not limited to: Perform molecular genetic testing on clinical specimens Mastery of all laboratory standard operating procedures for specimen handling, processing, test analyses, and recording of test results including efficiencies, high complexity troubleshooting procedures, and non-routine operations May supervise laboratory personnel Demonstrate ownership and timely completion of assigned or assumed tasks, including e-mails, paperwork and documentation, and nonconformances with appropriate prioritization and urgency and minimal supervision Demonstrate skill and reliability in leadership situations, including the appropriate handling of training, personnel issues, conflict resolution, and delicate subject matters. Report personnel and laboratory processing issues to management and participate/ engage in conflict resolution Contribute to and participate with activities associated with quality assurance, regulatory compliance, and continuous improvement (e.g., SOP revision/updates, monthly QA meetings, inspections, etc.) Perform, review and document laboratory quality control procedures in accordance with the Quality Assurance Program Prepare reagents required for laboratory testing Engage in training and perform competency assessment Perform proficiency testing for the clinical tests Assist in research and validation activities Independently identify and troubleshoot complex issues that could potentially adversely affect test performance Document all corrective actions taken when test systems deviate from the laboratory's established performance specifications Follow the laboratory’s standard operating procedures for quality and environmental health and safety and reporting all concerns of test quality and/or safety to the Lab’s Management or Safety Officer Ensure all work is performed in accordance with local, state, and federal regulations and participate in all regulatory inspections Work cooperatively in a team environment supporting fellow laboratory and management staff, which may include actively managing employees Perform any other site/lab specific duties as assigned Qualifications: To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skills and/or abilities required. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions. Who You Are: Active California Department of Public Health Clinical Laboratory Scientist (CLS) license or Clinical Genetic Molecular Biology Scientist (CGMBS) license (no exceptions) Experience in high complexity clinical laboratory testing, preferably in molecular diagnostics Performance of molecular testing (PCR, Microarray, Sanger/NGS sequencing) a plus Has at least 4 years of experience in molecular laboratory that demonstrate proficiency and independence in a clinical laboratory setting Must have strong analytical and problem-solving skills Must be detail-oriented and comfortable with technology Must have excellent verbal and written communication skills&nbsp; Strong computer skills across diverse platforms Excellent interpersonal communication and team player attitude Ability to adapt to change and a rapid work pace Maintains continuing education units required by California Department of Health Services and New York State Department of Health Physical Requirements: Repetitive movement of hands, arms and leg, fingers (typing and/or writing) Gripping/grasping Reaching above/below shoulder level Sitting, with occasional walking, standing, stooping and moving about Exposure to general office environment conditions Occasionally required to lift up to 25 pounds The final salary offered to a successful candidate will be dependent on several factors that may include but are not limited to the type and length of experience within the job, type and length of experience within the industry, education, etc. Base pay is one part of the Total Package that is provided to compensate and recognize employees for their work, and this role may be eligible for additional discretionary bonuses/incentives, and restricted stock units. Veracyte is a multi-state employer, and this salary range may not reflect positions that work in other states.Pay range$54&mdash;$63 USD&nbsp; What We Can Offer You Veracyte is a growing company that offers significant career opportunities if you are curious, driven, patient-oriented and aspire to help us build a great company. We offer competitive compensation and benefits, and are committed to fostering an inclusive workforce, where diverse backgrounds are represented, engaged, and empowered to drive innovative ideas and decisions. We are thrilled to be recognized as a 2024 Certified™ Great Place to Work® in both the US and Israel - a testament to our dynamic, inclusive, and inspiring workplace where passion meets purpose. &nbsp; About Veracyte Veracyte&nbsp;(Nasdaq: VCYT) is a global genomic diagnostics company that improves patient care by providing answers to clinical questions, informing diagnosis and treatment decisions throughout the patient journey in cancer and other diseases. The company’s growing menu of genomic tests leverage advances in genomic science and technology, enabling patients to avoid risky, costly diagnostic procedures and quicken time to appropriate treatment. The company’s tests in lung cancer, prostate cancer, breast cancer, thyroid cancer, bladder cancer and idiopathic pulmonary fibrosis are available to patients and its lymphoma subtyping and renal cancer tests are in development. With Veracyte’s exclusive global license to a best-in-class diagnostics instrument platform, the company is positioned to deliver its tests to patients worldwide.&nbsp;Veracyte&nbsp;is based in&nbsp;South San Francisco, California. For more information, please visit&nbsp;www.veracyte.com and follow the company on X (Formerly Twitter). Veracyte, Inc. is an Equal Opportunity Employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status or disability status. Veracyte participates in E-Verify in the United States. View our&nbsp;CCPA Disclosure Notice. If you receive any suspicious alerts or communications through LinkedIn or other online job sites for any position at Veracyte, please exercise caution and promptly report any concerns to careers@veracyte.com

Clinical Lab Scientist Lead

At Veracyte, we offer exciting career opportunities for those interested in joining a pioneering team that is committed to transforming cancer care for patients across the globe. Working at Veracyte enables our employees to not only make a meaningful impact on the lives of patients, but to also learn and grow within a purpose driven&nbsp;environment. This is what we call the Veracyte way&nbsp;– it’s about how we work together, guided by our values, to give clinicians the insights they need to help patients make life-changing decisions.&nbsp; Our Values: We Seek A Better Way: We innovate boldly, learn from our setbacks, and are resilient in our pursuit to transform cancer care We Make It Happen: We act with urgency, commit to quality, and bring fun to our hard work We Are Stronger Together:&nbsp;We collaborate openly, seek to understand, and celebrate our wins We Care Deeply: We embrace our differences, do the right thing, and encourage each other &nbsp;The Position: The Lead Clinical Laboratory Scientist is responsible for performing high complexity clinical laboratory testing on patient specimens, reviewing and reporting patient results, performing quality control and quality assurance activities and complying with all applicable local, state and federal laboratory, quality, and safety requirements. The high complexity nature of the work requires excellent attention to detail, effective written and verbal communication skills, and the ability to multitask and be flexible with tasks and schedules and the ability to work independently and effectively in a team environment. This is an onsite role in San Diego working Tuesday - Saturday from 5:00am - 1:30pm Essential Duties &amp; Responsibilities&nbsp; The main duties and responsibilities of the Lead Clinical Laboratory Scientist include the following, but not limited to: Perform molecular genetic testing on clinical specimens Mastery of all laboratory standard operating procedures for specimen handling, processing, test analyses, and recording of test results including efficiencies, high complexity troubleshooting procedures, and non-routine operations May supervise laboratory personnel Demonstrate ownership and timely completion of assigned or assumed tasks, including e-mails, paperwork and documentation, and nonconformances with appropriate prioritization and urgency and minimal supervision Demonstrate skill and reliability in leadership situations, including the appropriate handling of training, personnel issues, conflict resolution, and delicate subject matters. Report personnel and laboratory processing issues to management and participate/ engage in conflict resolution Contribute to and participate with activities associated with quality assurance, regulatory compliance, and continuous improvement (e.g., SOP revision/updates, monthly QA meetings, inspections, etc.) Perform, review and document laboratory quality control procedures in accordance with the Quality Assurance Program Prepare reagents required for laboratory testing Engage in training and perform competency assessment Perform proficiency testing for the clinical tests Assist in research and validation activities Independently identify and troubleshoot complex issues that could potentially adversely affect test performance Document all corrective actions taken when test systems deviate from the laboratory's established performance specifications Follow the laboratory’s standard operating procedures for quality and environmental health and safety and reporting all concerns of test quality and/or safety to the Lab’s Management or Safety Officer Ensure all work is performed in accordance with local, state, and federal regulations and participate in all regulatory inspections Work cooperatively in a team environment supporting fellow laboratory and management staff, which may include actively managing employees Perform any other site/lab specific duties as assigned Qualifications: To perform this job successfully, an individual must be able to perform each essential duty satisfactorily. The requirements listed below are representative of the knowledge, skills and/or abilities required. Reasonable accommodation may be made to enable individuals with disabilities to perform the essential functions. Who You Are: Active California Department of Public Health Clinical Laboratory Scientist (CLS) license or Clinical Genetic Molecular Biology Scientist (CGMBS) license (no exceptions) Experience in high complexity clinical laboratory testing, preferably in molecular diagnostics Performance of molecular testing (PCR, Microarray, Sanger/NGS sequencing) a plus Has at least 4 years of experience in molecular laboratory that demonstrate proficiency and independence in a clinical laboratory setting Must have strong analytical and problem-solving skills Must be detail-oriented and comfortable with technology Must have excellent verbal and written communication skills&nbsp; Strong computer skills across diverse platforms Excellent interpersonal communication and team player attitude Ability to adapt to change and a rapid work pace Maintains continuing education units required by California Department of Health Services and New York State Department of Health Physical Requirements: Repetitive movement of hands, arms and leg, fingers (typing and/or writing) Gripping/grasping Reaching above/below shoulder level Sitting, with occasional walking, standing, stooping and moving about Exposure to general office environment conditions Occasionally required to lift up to 25 pounds The final salary offered to a successful candidate will be dependent on several factors that may include but are not limited to the type and length of experience within the job, type and length of experience within the industry, education, etc. Base pay is one part of the Total Package that is provided to compensate and recognize employees for their work, and this role may be eligible for additional discretionary bonuses/incentives, and restricted stock units. Veracyte is a multi-state employer, and this salary range may not reflect positions that work in other states.Pay range$54&mdash;$63 USD&nbsp; What We Can Offer You Veracyte is a growing company that offers significant career opportunities if you are curious, driven, patient-oriented and aspire to help us build a great company. We offer competitive compensation and benefits, and are committed to fostering an inclusive workforce, where diverse backgrounds are represented, engaged, and empowered to drive innovative ideas and decisions. We are thrilled to be recognized as a 2024 Certified™ Great Place to Work® in both the US and Israel - a testament to our dynamic, inclusive, and inspiring workplace where passion meets purpose. &nbsp; About Veracyte Veracyte&nbsp;(Nasdaq: VCYT) is a global genomic diagnostics company that improves patient care by providing answers to clinical questions, informing diagnosis and treatment decisions throughout the patient journey in cancer and other diseases. The company’s growing menu of genomic tests leverage advances in genomic science and technology, enabling patients to avoid risky, costly diagnostic procedures and quicken time to appropriate treatment. The company’s tests in lung cancer, prostate cancer, breast cancer, thyroid cancer, bladder cancer and idiopathic pulmonary fibrosis are available to patients and its lymphoma subtyping and renal cancer tests are in development. With Veracyte’s exclusive global license to a best-in-class diagnostics instrument platform, the company is positioned to deliver its tests to patients worldwide.&nbsp;Veracyte&nbsp;is based in&nbsp;South San Francisco, California. For more information, please visit&nbsp;www.veracyte.com and follow the company on X (Formerly Twitter). Veracyte, Inc. is an Equal Opportunity Employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status or disability status. Veracyte participates in E-Verify in the United States. View our&nbsp;CCPA Disclosure Notice. If you receive any suspicious alerts or communications through LinkedIn or other online job sites for any position at Veracyte, please exercise caution and promptly report any concerns to careers@veracyte.com

At Veracyte, we offer exciting career opportunities for those interested in joining a pioneering team that is committed to transforming cancer care for patients across the globe. Working at Veracyte enables our employees to not only make a meaningful impact on the lives of patients, but to also learn and grow within a purpose driven&nbsp;environment. This is what we call the Veracyte way&nbsp;– it’s about how we work together, guided by our values, to give clinicians the insights they need to help patients make life-changing decisions.&nbsp; Our Values: We Seek A Better Way: We innovate boldly, learn from our setbacks, and are resilient in our pursuit to transform cancer care We Make It Happen: We act with urgency, commit to quality, and bring fun to our hard work We Are Stronger Together:&nbsp;We collaborate openly, seek to understand, and celebrate our wins We Care Deeply: We embrace our differences, do the right thing, and encourage each other &nbsp;The Position: We are looking for a highly motivated individual to join the Veracyte R&amp;D Team as a Scientist II in a contract position for one year. Being that this is a temporary contract position, this position is not eligible for a bonus or equity.&nbsp; This position requires planning and executing technical studies aimed at evaluating the performance of molecular in vitro diagnostic tests in the field of oncology.&nbsp; To be a successful candidate, we would like you to share our commitment to teamwork and collaboration and be excited by the challenges of applying your scientific expertise to develop genomic tests that improve patient diagnosis and treatment.&nbsp; Responsibilities: Participate in diagnostic test development, inclusive of development and verification testing, to ensure that IVD products conform to product specifications. Assist in writing technical reports related to experimental studies testing new or existing diagnostic products that become part of the Design History File and regulatory filings. Collaborate with technical team members to conduct laboratory experiments and document testing. Interact with multi-disciplinary teams such as the data analysis team to coordinate data transfer Who You Are: Education: PhD in chemistry, biochemistry or molecular biology (or related studies) plus extensive relevant industry experience (5+ years), or an B.S./M.S. in chemistry, biochemistry or molecular biology (or related studies) with additional relevant experience (8 + years).&nbsp; Prior experience in developing and/or verifying molecular IVD assays, genomics assays, or laboratory developed tests is required Experience with molecular platforms (e.g. next-generation sequencing, microarrays and/or qPCR) in the context of assay development and testing clinical specimens. Experience with qPCR or NGS protocols is strongly preferred Hands-on knowledge of the biochemistry underlying multi-component molecular biology methods at the sample preparation and assay level Strong organizational, communication, and interpersonal skills; including demonstrated ability to work well with others in team environment Ability to translate experimental results into technical reports and presentations Familiarity with IVD regulations (FDA 21 CFR Parts 820 and ISO 13485:2016) or CLIA regulations is desired &nbsp; #LI-Onsite &nbsp;The final salary offered to a successful candidate will be dependent on several factors that may include but are not limited to the type and length of experience within the job, type and length of experience within the industry, education, etc. Base pay is one part of the Total Package that is provided to compensate and recognize employees for their work, and this role may be eligible for additional discretionary bonuses/incentives, and restricted stock units. Veracyte is a multi-state employer, and this salary range may not reflect positions that work in other states.Pay range$145,000&mdash;$158,000 USD&nbsp; What We Can Offer You Veracyte is a growing company that offers significant career opportunities if you are curious, driven, patient-oriented and aspire to help us build a great company. We offer competitive compensation and benefits, and are committed to fostering an inclusive workforce, where diverse backgrounds are represented, engaged, and empowered to drive innovative ideas and decisions. We are thrilled to be recognized as a 2024 Certified™ Great Place to Work® in both the US and Israel - a testament to our dynamic, inclusive, and inspiring workplace where passion meets purpose. &nbsp; About Veracyte Veracyte&nbsp;(Nasdaq: VCYT) is a global genomic diagnostics company that improves patient care by providing answers to clinical questions, informing diagnosis and treatment decisions throughout the patient journey in cancer and other diseases. The company’s growing menu of genomic tests leverage advances in genomic science and technology, enabling patients to avoid risky, costly diagnostic procedures and quicken time to appropriate treatment. The company’s tests in lung cancer, prostate cancer, breast cancer, thyroid cancer, bladder cancer and idiopathic pulmonary fibrosis are available to patients and its lymphoma subtyping and renal cancer tests are in development. With Veracyte’s exclusive global license to a best-in-class diagnostics instrument platform, the company is positioned to deliver its tests to patients worldwide.&nbsp;Veracyte&nbsp;is based in&nbsp;South San Francisco, California. For more information, please visit&nbsp;www.veracyte.com and follow the company on X (Formerly Twitter). Veracyte, Inc. is an Equal Opportunity Employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status or disability status. Veracyte participates in E-Verify in the United States. View our&nbsp;CCPA Disclosure Notice. If you receive any suspicious alerts or communications through LinkedIn or other online job sites for any position at Veracyte, please exercise caution and promptly report any concerns to careers@veracyte.com

Contract Scientist II, Diagnostic Product Development

At Veracyte, we offer exciting career opportunities for those interested in joining a pioneering team that is committed to transforming cancer care for patients across the globe. Working at Veracyte enables our employees to not only make a meaningful impact on the lives of patients, but to also learn and grow within a purpose driven&nbsp;environment. This is what we call the Veracyte way&nbsp;– it’s about how we work together, guided by our values, to give clinicians the insights they need to help patients make life-changing decisions.&nbsp; Our Values: We Seek A Better Way: We innovate boldly, learn from our setbacks, and are resilient in our pursuit to transform cancer care We Make It Happen: We act with urgency, commit to quality, and bring fun to our hard work We Are Stronger Together:&nbsp;We collaborate openly, seek to understand, and celebrate our wins We Care Deeply: We embrace our differences, do the right thing, and encourage each other &nbsp;The Position: As a Customer Care Associate (CCA), you’ll be at the heart of our mission to deliver exceptional service and support to physicians, patients, pathology labs, and internal teams. In this role, you’ll manage inbound and outbound communications, triage inquiries, coordinate logistics, and support lab operations across multiple product lines. You’ll work closely with cross-functional teams to ensure timely and accurate processing of requests, contributing directly to patient care and customer satisfaction. Responsibilities may vary depending on the product line and location you support—flexibility, adaptability, and a collaborative mindset are essential. The schedule is Monday-Friday. Working hours TBD based on candidate's location.&nbsp; Essential Responsibilities: Manage inbound and outbound communications across phone, email, and fax, ensuring inquiries are addressed or routed appropriately. Coordinate and collaborate with internal teams (Customer Care, Sales, Lab, Billing, Pathology Labs) to support case resolution and ensure timely sample receipt. Document and maintain accurate records in LIS and Salesforce, including requisitions, call notes, and case updates. Support product-specific workflows, such as tissue procurement, report distribution, insurance follow-ups, and shipping coordination. Contribute to a positive customer experience by resolving issues efficiently and professionally across multiple product lines. Participate in process improvement efforts by sharing feedback and helping refine support procedures. Ensure compliance with healthcare regulations and company policies in all aspects of work. Who You Are: A Bachelor’s Degree (B.A. or B.S.) is preferred. Relevant experience may be considered in lieu of the education preference. 1–2 years of customer service experience in healthcare or life sciences (strongly preferred). #LI-Remote &nbsp;The final salary offered to a successful candidate will be dependent on several factors that may include but are not limited to the type and length of experience within the job, type and length of experience within the industry, education, etc. Base pay is one part of the Total Package that is provided to compensate and recognize employees for their work, and this role may be eligible for additional discretionary bonuses/incentives, and restricted stock units. Veracyte is a multi-state employer, and this salary range may not reflect positions that work in other states.Pay range$21&mdash;$23 USD&nbsp; What We Can Offer You Veracyte is a growing company that offers significant career opportunities if you are curious, driven, patient-oriented and aspire to help us build a great company. We offer competitive compensation and benefits, and are committed to fostering an inclusive workforce, where diverse backgrounds are represented, engaged, and empowered to drive innovative ideas and decisions. We are thrilled to be recognized as a 2024 Certified™ Great Place to Work® in both the US and Israel - a testament to our dynamic, inclusive, and inspiring workplace where passion meets purpose. &nbsp; About Veracyte Veracyte&nbsp;(Nasdaq: VCYT) is a global genomic diagnostics company that improves patient care by providing answers to clinical questions, informing diagnosis and treatment decisions throughout the patient journey in cancer and other diseases. The company’s growing menu of genomic tests leverage advances in genomic science and technology, enabling patients to avoid risky, costly diagnostic procedures and quicken time to appropriate treatment. The company’s tests in lung cancer, prostate cancer, breast cancer, thyroid cancer, bladder cancer and idiopathic pulmonary fibrosis are available to patients and its lymphoma subtyping and renal cancer tests are in development. With Veracyte’s exclusive global license to a best-in-class diagnostics instrument platform, the company is positioned to deliver its tests to patients worldwide.&nbsp;Veracyte&nbsp;is based in&nbsp;South San Francisco, California. For more information, please visit&nbsp;www.veracyte.com and follow the company on X (Formerly Twitter). Veracyte, Inc. is an Equal Opportunity Employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status or disability status. Veracyte participates in E-Verify in the United States. View our&nbsp;CCPA Disclosure Notice. If you receive any suspicious alerts or communications through LinkedIn or other online job sites for any position at Veracyte, please exercise caution and promptly report any concerns to careers@veracyte.com

Customer Care Associate

At Veracyte, we offer exciting career opportunities for those interested in joining a pioneering team that is committed to transforming cancer care for patients across the globe. Working at Veracyte enables our employees to not only make a meaningful impact on the lives of patients, but to also learn and grow within a purpose driven&nbsp;environment. This is what we call the Veracyte way&nbsp;– it’s about how we work together, guided by our values, to give clinicians the insights they need to help patients make life-changing decisions.&nbsp; Our Values: We Seek A Better Way: We innovate boldly, learn from our setbacks, and are resilient in our pursuit to transform cancer care We Make It Happen: We act with urgency, commit to quality, and bring fun to our hard work We Are Stronger Together:&nbsp;We collaborate openly, seek to understand, and celebrate our wins We Care Deeply: We embrace our differences, do the right thing, and encourage each other &nbsp;The Position: As a Cybersecurity Engineer at Veracyte, you will play a pivotal role in securing our digital infrastructure, monitoring for threats, and implementing cutting-edge cybersecurity solutions. You will work collaboratively with our IT and cybersecurity teams to protect our organization from cyber threats and ensure the confidentiality, integrity, and availability of our systems and data. Location: This is a hybrid position based in our San Diego office. Based on candidate location, we may consider (PST) remote. Responsibilities: Cybersecurity Infrastructure Management:&nbsp;- Design, implement, and maintain security infrastructure, including firewalls, intrusiondetection/prevention systems, VPNs, and other security-related technologies.&nbsp;- Conduct regular security assessments and vulnerability scans, identifying and mitigatingpotential vulnerabilities. Threat Monitoring and Incident Response:&nbsp;- Monitor network and system logs for suspicious activities and potential security incidents.&nbsp;- Develop and execute incident response plans to effectively manage and mitigatecybersecurity incidents.&nbsp;- Investigate security breaches and provide recommendations for improvements. Policy and Compliance:&nbsp;- Ensure compliance with industry-specific regulations and standards (e.g., GDPR, HIPAA, NISTCSF).&nbsp;- Assist in the development and enforcement of cybersecurity policies, standards, andprocedures.&nbsp;- Conduct security awareness training for employees to promote a culture of security. Security Tools and Technologies:&nbsp;- Evaluate and implement advanced cybersecurity tools and technologies to enhance oursecurity posture.&nbsp;- Stay updated on emerging threats and trends in the cybersecurity field and recommendproactive measures. Security Audits and Assessments:&nbsp;- Collaborate with external auditors and assessors to conduct security audits and assessments.&nbsp;- Work on remediation plans to address identified weaknesses. Collaboration and Communication:&nbsp;- Collaborate with cross-functional teams to integrate security into the development anddeployment processes.&nbsp;- Communicate cybersecurity risks and strategies to technical and non-technical stakeholders. Who You Are: Bachelor's degree in Computer Science, Information Security, or a related field. Relevant industry certifications such as CEH, Pentest+, CySA+, SSCP, OSCP, orequivalent. 5 or more years experience in cybersecurity engineering or a related cybersecurity role.Proficiency in security tools and technologies, including firewalls, SIEM, IDS/IPS, andantivirus solutions. Strong understanding of network protocols, architecture, and security bestpractices. Knowledge of regulatory requirements and industry standards. Excellent problem-solving and analytical skills. Strong communication and teamwork skills. Experience with scripting and automation (e.g., Python, PowerShell) #LI-Hybrid&nbsp; &nbsp;The final salary offered to a successful candidate will be dependent on several factors that may include but are not limited to the type and length of experience within the job, type and length of experience within the industry, education, etc. Base pay is one part of the Total Package that is provided to compensate and recognize employees for their work, and this role may be eligible for additional discretionary bonuses/incentives, and restricted stock units. Veracyte is a multi-state employer, and this salary range may not reflect positions that work in other states.Pay range$130,000&mdash;$150,000 USD&nbsp; What We Can Offer You Veracyte is a growing company that offers significant career opportunities if you are curious, driven, patient-oriented and aspire to help us build a great company. We offer competitive compensation and benefits, and are committed to fostering an inclusive workforce, where diverse backgrounds are represented, engaged, and empowered to drive innovative ideas and decisions. We are thrilled to be recognized as a 2024 Certified™ Great Place to Work® in both the US and Israel - a testament to our dynamic, inclusive, and inspiring workplace where passion meets purpose. &nbsp; About Veracyte Veracyte&nbsp;(Nasdaq: VCYT) is a global genomic diagnostics company that improves patient care by providing answers to clinical questions, informing diagnosis and treatment decisions throughout the patient journey in cancer and other diseases. The company’s growing menu of genomic tests leverage advances in genomic science and technology, enabling patients to avoid risky, costly diagnostic procedures and quicken time to appropriate treatment. The company’s tests in lung cancer, prostate cancer, breast cancer, thyroid cancer, bladder cancer and idiopathic pulmonary fibrosis are available to patients and its lymphoma subtyping and renal cancer tests are in development. With Veracyte’s exclusive global license to a best-in-class diagnostics instrument platform, the company is positioned to deliver its tests to patients worldwide.&nbsp;Veracyte&nbsp;is based in&nbsp;South San Francisco, California. For more information, please visit&nbsp;www.veracyte.com and follow the company on X (Formerly Twitter). Veracyte, Inc. is an Equal Opportunity Employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status or disability status. Veracyte participates in E-Verify in the United States. View our&nbsp;CCPA Disclosure Notice. If you receive any suspicious alerts or communications through LinkedIn or other online job sites for any position at Veracyte, please exercise caution and promptly report any concerns to careers@veracyte.com

Cybersecurity Engineer

At Veracyte, we offer exciting career opportunities for those interested in joining a pioneering team that is committed to transforming cancer care for patients across the globe. Working at Veracyte enables our employees to not only make a meaningful impact on the lives of patients, but to also learn and grow within a purpose driven&nbsp;environment. This is what we call the Veracyte way&nbsp;– it’s about how we work together, guided by our values, to give clinicians the insights they need to help patients make life-changing decisions.&nbsp; Our Values: We Seek A Better Way: We innovate boldly, learn from our setbacks, and are resilient in our pursuit to transform cancer care We Make It Happen: We act with urgency, commit to quality, and bring fun to our hard work We Are Stronger Together:&nbsp;We collaborate openly, seek to understand, and celebrate our wins We Care Deeply: We embrace our differences, do the right thing, and encourage each other &nbsp;The Position Veracyte is revolutionizing cancer diagnostics through advanced genomic technologies and data-driven innovation. Our Israel team plays a crucial role in developing scalable infrastructure to support AI-enabled insights across research and clinical applications. We’re seeking a skilled Data Engineer to develop robust, scalable data infrastructure and integrate cutting-edge AI and agent-based technologies into our genomic data processes. You'll be a core contributor in designing and implementing cloud-based data pipelines, while embedding AI models and intelligent agent frameworks into our analytic workflows. This role blends engineering excellence with innovation. You’ll collaborate closely with R&amp;D, and data science teams to deliver high-quality, cloud-native analytics platforms that accelerate research and clinical impact. This is a hybrid role based out of our Haifa, Israel office.&nbsp; Key Responsibilities Design and build cloud-native data pipelines (AWS) for large-scale genomic analytics Integrate AI/ML models, agent-based tools, and MCP protocols into data workflows Automate and optimize CI/CD processes for research and production environments Collaborate with cross-functional teams to define and implement robust data architectures Develop tools for data ingestion, transformation, and quality monitoring Ensure data integrity, reproducibility, and compliance with regulatory standards &nbsp; Who You Are: 4+ years in data engineering or backend software engineering Bachelor's degree in Software Engineering, relevant technical field, or equivalent Technologically diverse background and ability/willingness to learn new things quickly Strong Python, SQL and Bash scripting skills Hands-on experience with AWS (e.g., S3, Lambda, ECS, EKS, Sagemaker) Familiarity with containerization (Docker) and orchestration Experience with Apache Airflow for workflow orchestration and scheduling Experience building CI/CD pipelines Understanding of MCP (Model Context Protocol) and its role in AI system design Knowledge of data lake architecture, structured/unstructured data handling Familiarity with machine learning pipelines or MLOps frameworks Experience with SQL and NoSQL databases and building ELT/ETL pipelines Preferred Skills Background in biotech, healthcare, or regulated industries Experience with Apache Spark or distributed data processing Proven track record in deploying AI systems in production Why Join Us Mission-driven impact: Your work directly contributes to saving lives Forward-thinking team: Collaborate with experts in AI, genomics, and data engineering Cutting-edge stack: Work with the latest tools to bring AI into data-centric infrastructure #LI-Remote &nbsp;&nbsp; What We Can Offer You Veracyte is a growing company that offers significant career opportunities if you are curious, driven, patient-oriented and aspire to help us build a great company. We offer competitive compensation and benefits, and are committed to fostering an inclusive workforce, where diverse backgrounds are represented, engaged, and empowered to drive innovative ideas and decisions. We are thrilled to be recognized as a 2024 Certified™ Great Place to Work® in both the US and Israel - a testament to our dynamic, inclusive, and inspiring workplace where passion meets purpose. &nbsp; About Veracyte Veracyte&nbsp;(Nasdaq: VCYT) is a global genomic diagnostics company that improves patient care by providing answers to clinical questions, informing diagnosis and treatment decisions throughout the patient journey in cancer and other diseases. The company’s growing menu of genomic tests leverage advances in genomic science and technology, enabling patients to avoid risky, costly diagnostic procedures and quicken time to appropriate treatment. The company’s tests in lung cancer, prostate cancer, breast cancer, thyroid cancer, bladder cancer and idiopathic pulmonary fibrosis are available to patients and its lymphoma subtyping and renal cancer tests are in development. With Veracyte’s exclusive global license to a best-in-class diagnostics instrument platform, the company is positioned to deliver its tests to patients worldwide.&nbsp;Veracyte&nbsp;is based in&nbsp;South San Francisco, California. For more information, please visit&nbsp;www.veracyte.com and follow the company on X (Formerly Twitter). Veracyte, Inc. is an Equal Opportunity Employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status or disability status. Veracyte participates in E-Verify in the United States. View our&nbsp;CCPA Disclosure Notice. If you receive any suspicious alerts or communications through LinkedIn or other online job sites for any position at Veracyte, please exercise caution and promptly report any concerns to careers@veracyte.com

Data Engineer

At Veracyte, we offer exciting career opportunities for those interested in joining a pioneering team that is committed to transforming cancer care for patients across the globe. Working at Veracyte enables our employees to not only make a meaningful impact on the lives of patients, but to also learn and grow within a purpose driven&nbsp;environment. This is what we call the Veracyte way&nbsp;– it’s about how we work together, guided by our values, to give clinicians the insights they need to help patients make life-changing decisions.&nbsp; Our Values: We Seek A Better Way: We innovate boldly, learn from our setbacks, and are resilient in our pursuit to transform cancer care We Make It Happen: We act with urgency, commit to quality, and bring fun to our hard work We Are Stronger Together:&nbsp;We collaborate openly, seek to understand, and celebrate our wins We Care Deeply: We embrace our differences, do the right thing, and encourage each other &nbsp;The Position: The Data Scientist on the Veracyte Data Engineering team will leverage data from diverse internal and external sources to derive actionable insights, develop predictive models, and support the company’s mission of improving diagnostic accuracy. This role collaborates closely with data engineers, the Technical Program Manager (TPM), and cross-functional teams in a Scrum environment to deliver high-impact data solutions aligned with Veracyte’s global data strategy and digital transformation goals. The position is based out of our San Diego office (hybrid) and we are also open to US Remote (working PST hours). Key Responsibilities Data Analysis and Modeling: Analyze large, complex datasets from the Veracyte Lakehouse (e.g., genomic, clinical, operational data) to identify trends and patterns. Develop and deploy machine learning models using tools like Amazon SageMaker and Python for applications such as biomarker discovery and clinical decision support. Collaboration and Requirement Gathering: Work with the TPM and stakeholders to define data science requirements and user stories for inclusion in the team’s Jira backlog. Partner with data engineers to ensure data pipelines and cataloged datasets meet analytical needs. Model Development and Optimization: Build, validate, and refine AI/ML models (e.g., LLM refinement, Verachat RAG) to support AI training and operational dashboards. Optimize models for performance and scalability within cloud environments like AWS and Snowflake. Data Interpretation and Reporting: Translate data insights into actionable recommendations for business operations, R&amp;D, and healthcare providers. Create visualizations and reports to communicate findings to technical and non-technical audiences. Support Data Strategy: Contribute to the development of data-driven strategies by providing analytical expertise. Ensure models and analyses comply with data governance and security policies. Knowledge Sharing: Mentor junior team members and promote a culture of continuous learning in data science practices. Stay updated on emerging tools and techniques to enhance team capabilities. Who You Are: Education: Bachelor’s or Master’s degree in Data Science, Computer Science, Statistics, or a related field. Experience: 3+ years (BS) or 1+ years (MS) of experience in data science or a similar role. Experience with healthcare or genomic data is a plus. Technical Skills: Proficiency in Python, R, or similar languages for data analysis and modeling. Experience with AWS services (e.g., SageMaker, Redshift) and Snowflake for data processing and storage. Familiarity with machine learning frameworks (e.g., TensorFlow, PyTorch) and data visualization tools (e.g., Matplotlib, Tableau). Knowledge of SQL and data cataloging concepts is advantageous. Soft Skills: Strong analytical and problem-solving skills. Excellent communication skills to collaborate with cross-functional teams in a Scrum setting. Ability to work effectively in a fast-paced, innovative environment. &nbsp; #LI-Hybrid, or #LI-Remote &nbsp;The final salary offered to a successful candidate will be dependent on several factors that may include but are not limited to the type and length of experience within the job, type and length of experience within the industry, education, etc. Base pay is one part of the Total Package that is provided to compensate and recognize employees for their work, and this role may be eligible for additional discretionary bonuses/incentives, and restricted stock units. Veracyte is a multi-state employer, and this salary range may not reflect positions that work in other states.Pay range$130,000&mdash;$150,000 USD&nbsp; What We Can Offer You Veracyte is a growing company that offers significant career opportunities if you are curious, driven, patient-oriented and aspire to help us build a great company. We offer competitive compensation and benefits, and are committed to fostering an inclusive workforce, where diverse backgrounds are represented, engaged, and empowered to drive innovative ideas and decisions. We are thrilled to be recognized as a 2024 Certified™ Great Place to Work® in both the US and Israel - a testament to our dynamic, inclusive, and inspiring workplace where passion meets purpose. &nbsp; About Veracyte Veracyte&nbsp;(Nasdaq: VCYT) is a global genomic diagnostics company that improves patient care by providing answers to clinical questions, informing diagnosis and treatment decisions throughout the patient journey in cancer and other diseases. The company’s growing menu of genomic tests leverage advances in genomic science and technology, enabling patients to avoid risky, costly diagnostic procedures and quicken time to appropriate treatment. The company’s tests in lung cancer, prostate cancer, breast cancer, thyroid cancer, bladder cancer and idiopathic pulmonary fibrosis are available to patients and its lymphoma subtyping and renal cancer tests are in development. With Veracyte’s exclusive global license to a best-in-class diagnostics instrument platform, the company is positioned to deliver its tests to patients worldwide.&nbsp;Veracyte&nbsp;is based in&nbsp;South San Francisco, California. For more information, please visit&nbsp;www.veracyte.com and follow the company on X (Formerly Twitter). Veracyte, Inc. is an Equal Opportunity Employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status or disability status. Veracyte participates in E-Verify in the United States. View our&nbsp;CCPA Disclosure Notice. If you receive any suspicious alerts or communications through LinkedIn or other online job sites for any position at Veracyte, please exercise caution and promptly report any concerns to careers@veracyte.com

Data Scientist

At Veracyte, we offer exciting career opportunities for those interested in joining a pioneering team that is committed to transforming cancer care for patients across the globe. Working at Veracyte enables our employees to not only make a meaningful impact on the lives of patients, but to also learn and grow within a purpose driven&nbsp;environment. This is what we call the Veracyte way&nbsp;– it’s about how we work together, guided by our values, to give clinicians the insights they need to help patients make life-changing decisions.&nbsp; Our Values: We Seek A Better Way: We innovate boldly, learn from our setbacks, and are resilient in our pursuit to transform cancer care We Make It Happen: We act with urgency, commit to quality, and bring fun to our hard work We Are Stronger Together:&nbsp;We collaborate openly, seek to understand, and celebrate our wins We Care Deeply: We embrace our differences, do the right thing, and encourage each other &nbsp;&nbsp; The Position: We are looking for an experienced data scientist to empower our medical diagnostic capabilities. As an integral part of our R&amp;D, you will be called on to research and develop data-centric analytic methods. The successful candidate will be in charge of researching and developing algorithmic pipeline across various system levels, from raw genomic data processing, through features extraction up to machine learning, statistical assessment and optimization.&nbsp;&nbsp; The successful candidate will be an essential team player for significant optimization of our growing genomic data analytic platform. This entails working cross-functionally with bioinformaticians, clinical analysts, software engineers and business analysts to ensure Veracyte's data becomes powerful asset and value growth driver. Specifically, the role assumes participation in the design and prototyping of cutting-edge deep learning, machine learning and statistical algorithms for analysis of genetic data to improve clinical performance, hacking the high-throughput data processing pipelines - to replace heavy repetitive computations with trained models, and utilize DL/ML on a system level to shorten the processing times and costs.&nbsp; The ideal candidate will have the ability to see the big picture and to understand user needs and requirements and to identify the opportunities for applying solutions from the deep learning, machine learning, algorithms and data science domains.&nbsp; This is a remote position based out of our Israel office. Send your resume directly to&nbsp;adi.eyal@veracyte.com&nbsp;- Adi Eyal, Human Resources, Israel office Responsibilities&nbsp; Analyze next-generation sequencing data ranging from single research experiments to very large data sets Research and develop novel deep &amp; machine learning architectures, statistical algorithms and mathematical models for application in genomics Lead the design and development of data specification standards and data science business processes Produce correct conclusions based on rigorous mathematical analysis and principles of statistics and probability Collaborate effectively with R&amp;D, production, and clinical teams to build pipelines for high-throughput sequencing data Be the "go to" person for data and algorithms issues Ensure internal processes and metrics are aligned to create the highest product quality and competitive advantage Develop Python software infrastructure to support algorithm testing and simulation studies Produce clear, concise and correct technical documentation including research reports and algorithm specifications Collaborate across the organization to build data application pipelines for high-throughput sequencing data&nbsp; Generating ideas to improve existing technology and drive future technology Who You Are: Master’s degree / PhD in engineering, computer science, bioinformatics, statistics, or similar, with a strong foundation in probability theory and/or statistics. At least 5-year practical experience in scientific methods, processes, algorithms and systems for knowledge and insights extraction from data Extensive knowledge in the domains of machine learning, signal processing and related quantitative techniques and theory Strong foundation in probability theory and/or statistics including parameter estimation and hypothesis testing Knowledge of core concepts in data analysis and applied statistics - model testing, regression, classification, clustering, data mining Good Python, bash and scripting fundamentals, including file parsing and data visualization Experience with cloud computing technologies (AWS preferred) - a plus Proficiency in at least one major deep learning framework (PyTorch, TensorFlow, MXNet) – a plus Knowledge of bioinformatics tools, clinical diagnostics workflows or genetic processes - a plus Experience with data management in a regulated environment - a plus Desire to learn about human genetics, genomics and next-generation sequencing technologies Highly organized and detail-oriented, with the ability to create clear and concise technical documentation Excellent verbal and written communication skills and the desire to work in a dynamic and collaborative environment Ability to work independently and remotely while maintaining a strong teamwork ethics Independent self-management and organizational skills Able to manage workload and set personal and project priorities Entrepreneurial, driven to create and to be impactful team player Relies on data more than gut instinct Puts the team harmony over their own self-interest, but data above all Strong attention to detail demonstrating accuracy in tracking and reporting data Flexibility to adjust quickly and effectively to frequent change and altered priorities Disciplined in following process consistently Eagerness to acquire new skills in areas such as databases, statistics, and genetics Excellent verbal and written communication Ability to evaluate and apply new technologies in a short time Send your resume directly to&nbsp;adi.eyal@veracyte.com&nbsp;- Adi Eyal, Human Resources, Israel office #LI-Remote &nbsp;&nbsp; What We Can Offer You Veracyte is a growing company that offers significant career opportunities if you are curious, driven, patient-oriented and aspire to help us build a great company. We offer competitive compensation and benefits, and are committed to fostering an inclusive workforce, where diverse backgrounds are represented, engaged, and empowered to drive innovative ideas and decisions. We are thrilled to be recognized as a 2024 Certified™ Great Place to Work® in both the US and Israel - a testament to our dynamic, inclusive, and inspiring workplace where passion meets purpose. &nbsp; About Veracyte Veracyte&nbsp;(Nasdaq: VCYT) is a global genomic diagnostics company that improves patient care by providing answers to clinical questions, informing diagnosis and treatment decisions throughout the patient journey in cancer and other diseases. The company’s growing menu of genomic tests leverage advances in genomic science and technology, enabling patients to avoid risky, costly diagnostic procedures and quicken time to appropriate treatment. The company’s tests in lung cancer, prostate cancer, breast cancer, thyroid cancer, bladder cancer and idiopathic pulmonary fibrosis are available to patients and its lymphoma subtyping and renal cancer tests are in development. With Veracyte’s exclusive global license to a best-in-class diagnostics instrument platform, the company is positioned to deliver its tests to patients worldwide.&nbsp;Veracyte&nbsp;is based in&nbsp;South San Francisco, California. For more information, please visit&nbsp;www.veracyte.com and follow the company on X (Formerly Twitter). Veracyte, Inc. is an Equal Opportunity Employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status or disability status. Veracyte participates in E-Verify in the United States. View our&nbsp;CCPA Disclosure Notice. If you receive any suspicious alerts or communications through LinkedIn or other online job sites for any position at Veracyte, please exercise caution and promptly report any concerns to careers@veracyte.com

At Veracyte, we offer exciting career opportunities for those interested in joining a pioneering team that is committed to transforming cancer care for patients across the globe. Working at Veracyte enables our employees to not only make a meaningful impact on the lives of patients, but to also learn and grow within a purpose driven&nbsp;environment. This is what we call the Veracyte way&nbsp;– it’s about how we work together, guided by our values, to give clinicians the insights they need to help patients make life-changing decisions.&nbsp; Our Values: We Seek A Better Way: We innovate boldly, learn from our setbacks, and are resilient in our pursuit to transform cancer care We Make It Happen: We act with urgency, commit to quality, and bring fun to our hard work We Are Stronger Together:&nbsp;We collaborate openly, seek to understand, and celebrate our wins We Care Deeply: We embrace our differences, do the right thing, and encourage each other &nbsp;The Position: This is a remote friendly position. On-site cube available in South San Francisco or San Diego. &nbsp; We are seeking a talented and experienced AI/ML data scientist to join our Veracyte’s Data Science team. This position offers a unique opportunity to work with experienced professionals to drive research and develop new diagnostic products employing one of the world’s largest clinical cancer databases, encompassing multi-platform digital pathology, genomic and clinical outcome data. &nbsp; The successful candidate will assist in the development of digital pathology AI models for a wide range of clinical and pathology outcomes by applying and adapting state-of-the-art vision/vision-language foundation models to whole-slide images (WSIs). As a Data Scientist II at Veracyte, the candidate will be expected to adapt and develop solutions to complex problems under company’s objective. This work will be conducted in close collaboration with other teams, including internal medical and business development teams, as well as key opinion leaders, with whom we collaborate on identifying relevant data, and developing computer vision models. The ability to explain AI/ML concepts to both experts and non-experts, including formal presentation, academic writing, and generation of publication-quality figures will be key necessary talents. The ideal candidate is passionate about data, eager to learn independently, and possesses strong analytical, problem-solving, and storytelling skills. &nbsp; KEY RESPONSIBILITIES: &nbsp; Assist in the development of digital pathology AI (DPAI) models with WSI data to predict clinical outcome and pathological/morphologic features, including adapting open-source state-of-the-art AI foundation models to Veracyte’s data. &nbsp; Assist in the evaluation and analyzing of DPAI models with respect to clinical, pathological and genomic outcomes or features, with a view to linking explainability of model features to biology.&nbsp; Participate in the design and carry experiments to compare and evaluate DPAI methods. Document and explain the results.&nbsp; Collaborate with both internal and external partners to understand the clinical and business requirements for given products and tailor algorithms accordingly. &nbsp; &nbsp;Work with bioinformatician, statistician, and medical experts to document projects, including generating analyses and visualizations for publication in peer-reviewed journals.&nbsp; Who You Are: REQUIRED EXPERIENCE: &nbsp; PhD in Statistics, Biostatistics, Data Science or equivalent field. &nbsp; 3+ years of experience of data/applied scientist role or equivalent&nbsp; Proficient in Python or equivalent in carrying out AI development. &nbsp; Strong skills with data clean-up, manipulation and visualization using tidyverse, ggplot in R or equivalent. &nbsp; Experience in statistical analysis, especially in survival modelling and hypothesis testing (i.e., multivariate regression modelling with interaction effects). &nbsp; Excellent in summarizing and communicating findings from data and attention to detail. &nbsp; Ability to work effectively in a fast-paced and collaborative environment.&nbsp; Eagerness to learn new technologies and adapt to evolving requirements. &nbsp; RELEVANT EXPERIENCE (preferred but not required): &nbsp; Knowledge of cancer biology&nbsp; Experience working with real world clinical data.&nbsp; &nbsp; #LI-Hybrid, or #LI-Remote &nbsp;The final salary offered to a successful candidate will be dependent on several factors that may include but are not limited to the type and length of experience within the job, type and length of experience within the industry, education, etc. Base pay is one part of the Total Package that is provided to compensate and recognize employees for their work, and this role may be eligible for additional discretionary bonuses/incentives, and restricted stock units. Veracyte is a multi-state employer, and this salary range may not reflect positions that work in other states.Pay range$101,000&mdash;$140,000 USD&nbsp; What We Can Offer You Veracyte is a growing company that offers significant career opportunities if you are curious, driven, patient-oriented and aspire to help us build a great company. We offer competitive compensation and benefits, and are committed to fostering an inclusive workforce, where diverse backgrounds are represented, engaged, and empowered to drive innovative ideas and decisions. We are thrilled to be recognized as a 2024 Certified™ Great Place to Work® in both the US and Israel - a testament to our dynamic, inclusive, and inspiring workplace where passion meets purpose. &nbsp; About Veracyte Veracyte&nbsp;(Nasdaq: VCYT) is a global genomic diagnostics company that improves patient care by providing answers to clinical questions, informing diagnosis and treatment decisions throughout the patient journey in cancer and other diseases. The company’s growing menu of genomic tests leverage advances in genomic science and technology, enabling patients to avoid risky, costly diagnostic procedures and quicken time to appropriate treatment. The company’s tests in lung cancer, prostate cancer, breast cancer, thyroid cancer, bladder cancer and idiopathic pulmonary fibrosis are available to patients and its lymphoma subtyping and renal cancer tests are in development. With Veracyte’s exclusive global license to a best-in-class diagnostics instrument platform, the company is positioned to deliver its tests to patients worldwide.&nbsp;Veracyte&nbsp;is based in&nbsp;South San Francisco, California. For more information, please visit&nbsp;www.veracyte.com and follow the company on X (Formerly Twitter). Veracyte, Inc. is an Equal Opportunity Employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status or disability status. Veracyte participates in E-Verify in the United States. View our&nbsp;CCPA Disclosure Notice. If you receive any suspicious alerts or communications through LinkedIn or other online job sites for any position at Veracyte, please exercise caution and promptly report any concerns to careers@veracyte.com

Data Scientist II

At Veracyte, we offer exciting career opportunities for those interested in joining a pioneering team that is committed to transforming cancer care for patients across the globe. Working at Veracyte enables our employees to not only make a meaningful impact on the lives of patients, but to also learn and grow within a purpose driven&nbsp;environment. This is what we call the Veracyte way&nbsp;– it’s about how we work together, guided by our values, to give clinicians the insights they need to help patients make life-changing decisions.&nbsp; Our Values: We Seek A Better Way: We innovate boldly, learn from our setbacks, and are resilient in our pursuit to transform cancer care We Make It Happen: We act with urgency, commit to quality, and bring fun to our hard work We Are Stronger Together:&nbsp;We collaborate openly, seek to understand, and celebrate our wins We Care Deeply: We embrace our differences, do the right thing, and encourage each other &nbsp;The Position: This is a remote friendly position. On-site cube available in South San Francisco or San Diego. &nbsp; We are seeking a talented and experienced AI/ML data scientist to join our Veracyte’s Data Science team. This position offers a unique opportunity to work with experienced professionals to drive research and develop new diagnostic products employing one of the world’s largest clinical cancer databases, encompassing multi-platform digital pathology, genomic and clinical outcome data. &nbsp; The successful candidate will develop digital pathology AI models for a wide range of clinical and pathology outcomes by applying and adapting state-of-the-art vision/vision-language foundation models to whole-slide images (WSIs). As a Data Scientist III at Veracyte, the candidate will be expected to assist in developing innovative solutions to complex problems under company’s objective. This work will be conducted in close collaboration with other teams, including internal medical and business development teams, as well as key opinion leaders, with whom we collaborate on identifying relevant data, and developing computer vision models. The ability to explain AI/ML concepts to both experts and non-experts, including formal presentation, academic writing, and generation of publication-quality figures will be key necessary talents. The ideal candidate is passionate about data, eager to learn independently, and possesses strong analytical, problem-solving, and storytelling skills. &nbsp; KEY RESPONSIBILITIES: Develop digital pathology AI (DPAI) models with WSI data to predict clinical outcome and pathological/morphologic features, including adapting open-source state-of-the-art AI foundation models to Veracyte’s data. &nbsp; Evaluate and analyze DPAI models with respect to clinical, pathological and genomic outcomes or features, with a view to linking explainability of model features to biology.&nbsp; Design and carry experiments to compare and evaluate DPAI methods. Document and explain the results.&nbsp; Collaborate with both internal and external partners to understand the clinical and business requirements for given products and tailor algorithms accordingly. &nbsp; &nbsp;Work with bioinformatician, statistician, and medical experts to document projects, including generating analyses and visualizations for publication in peer-reviewed journals. &nbsp; Who You Are: REQUIRED EXPERIENCE: &nbsp; PhD in Data Science, Machine Learning, Applied Math or equivalent field. &nbsp; 5+ years of experience of data/applied scientist role or equivalent &nbsp; Expert in Python or equivalent language for AI/ML development in the context of computer vision / DPAI (this includes data manipulation and preparation.)&nbsp; Experience in statistical analysis, especially in survival modelling and hypothesis testing (i.e., multivariate regression modelling with interaction effects).&nbsp; Experience working in cloud computing environments (AWS preferred). &nbsp; Demonstrated proficiency in summarizing and communicating findings from data, including an attention to detail when sharing findings.&nbsp; Ability to work effectively in a fast-paced and collaborative environment. &nbsp; Eagerness to learn new technologies and adapt to evolving requirements. &nbsp; RELEVANT EXPERIENCE (preferred but not required): &nbsp; Knowledge of cancer biology&nbsp; Proficiency with documentation and submission in regulated diagnostic environments (LDT or IVD).&nbsp; Experience working with real world clinical data.&nbsp; &nbsp; #LI-Hybrid, or #LI-Remote &nbsp;The final salary offered to a successful candidate will be dependent on several factors that may include but are not limited to the type and length of experience within the job, type and length of experience within the industry, education, etc. Base pay is one part of the Total Package that is provided to compensate and recognize employees for their work, and this role may be eligible for additional discretionary bonuses/incentives, and restricted stock units. Veracyte is a multi-state employer, and this salary range may not reflect positions that work in other states.Pay range$130,000&mdash;$171,000 USD&nbsp; What We Can Offer You Veracyte is a growing company that offers significant career opportunities if you are curious, driven, patient-oriented and aspire to help us build a great company. We offer competitive compensation and benefits, and are committed to fostering an inclusive workforce, where diverse backgrounds are represented, engaged, and empowered to drive innovative ideas and decisions. We are thrilled to be recognized as a 2024 Certified™ Great Place to Work® in both the US and Israel - a testament to our dynamic, inclusive, and inspiring workplace where passion meets purpose. &nbsp; About Veracyte Veracyte&nbsp;(Nasdaq: VCYT) is a global genomic diagnostics company that improves patient care by providing answers to clinical questions, informing diagnosis and treatment decisions throughout the patient journey in cancer and other diseases. The company’s growing menu of genomic tests leverage advances in genomic science and technology, enabling patients to avoid risky, costly diagnostic procedures and quicken time to appropriate treatment. The company’s tests in lung cancer, prostate cancer, breast cancer, thyroid cancer, bladder cancer and idiopathic pulmonary fibrosis are available to patients and its lymphoma subtyping and renal cancer tests are in development. With Veracyte’s exclusive global license to a best-in-class diagnostics instrument platform, the company is positioned to deliver its tests to patients worldwide.&nbsp;Veracyte&nbsp;is based in&nbsp;South San Francisco, California. For more information, please visit&nbsp;www.veracyte.com and follow the company on X (Formerly Twitter). Veracyte, Inc. is an Equal Opportunity Employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status or disability status. Veracyte participates in E-Verify in the United States. View our&nbsp;CCPA Disclosure Notice. If you receive any suspicious alerts or communications through LinkedIn or other online job sites for any position at Veracyte, please exercise caution and promptly report any concerns to careers@veracyte.com

Data Scientist III

At Veracyte, we offer exciting career opportunities for those interested in joining a pioneering team that is committed to transforming cancer care for patients across the globe. Working at Veracyte enables our employees to not only make a meaningful impact on the lives of patients, but to also learn and grow within a purpose driven&nbsp;environment. This is what we call the Veracyte way&nbsp;– it’s about how we work together, guided by our values, to give clinicians the insights they need to help patients make life-changing decisions.&nbsp; Our Values: We Seek A Better Way: We innovate boldly, learn from our setbacks, and are resilient in our pursuit to transform cancer care We Make It Happen: We act with urgency, commit to quality, and bring fun to our hard work We Are Stronger Together:&nbsp;We collaborate openly, seek to understand, and celebrate our wins We Care Deeply: We embrace our differences, do the right thing, and encourage each other &nbsp;The Position: This is a remote friendly position. On-site cube available in South San Francisco or San Diego. &nbsp; We are seeking a talented and experienced data scientist to join our Data Analysis Team (DAT), as part of the R&amp;D group for Veracyte Inc. This position offers a unique opportunity to work with experienced professionals to carry out AI/ML modelling and analysis of the world’s largest database of cancer patients, encompassing multi-platform digital pathology, genomic and clinical outcome data. &nbsp; The primary objective of this role is to analysis millions of records of real-world insurance claims and EHR data to define clinical treatments and outcomes. The successful candidate needs to be proficient in state-of-art data extraction, transformation and loading (ETL), and statistical analysis to convert data into meaningful insights and stories. The candidate will also need to communicate and understand business needs, identify relevant data, process and analyze data accordingly. Experience of academic writing and prepare data/figures for manuscript are necessary for success in this position. The candidate should also be able to design graphics to explain AI models with known clinical or genomic features. Strong track record of publishing in both clinical and technical peer-review journals or conferences is highly desired. The ideal candidate is passionate about data, eager to learn independently, and possesses strong analytical, problem-solving, and storytelling skills. &nbsp; KEY RESPONSIBILITIES: &nbsp; Assist in analyzing real-world data to identify patterns for various clinical and business cases, including treatment patterns and management costs.&nbsp;&nbsp; Participate in Identifying key clinical events, such as cancer progression and treatments, using CPT, NDC, ICD codes, and structured database free text.&nbsp;&nbsp; Assist in conducting statistical analysis and survival modelling for the clinical events defined from real-world data.&nbsp;&nbsp;&nbsp; Ability to visualize finding from the data and summarize them in a coherent story. &nbsp; Support data scientists in developing digital pathology AI models&nbsp; Work with bioinformatician, statistician, and medical experts in manuscripts.&nbsp; Who You Are: REQUIRED EXPERIENCE: &nbsp; PhD in Statistics, Data Science, or equivalent field. &nbsp; 3+ years of experience of data/applied scientist role or equivalent.&nbsp; Experience in working with real-world data of insurance claims and EHR records&nbsp; Proficient in SQL and R. &nbsp; Strong skills with data clean-up, manipulation and visualization using tidyverse, ggplot in R or equivalent. &nbsp; Proficient in statistical analysis, especially in survival modelling and hypothesis testing (i.e., multivariate regression modelling with interaction effects).&nbsp; Experience working in cloud computing environments (AWS preferred). &nbsp; Demonstrated proficiency in summarizing and communicating findings from data, including an attention to detail when sharing findings.&nbsp; Ability to work effectively in a fast-paced and collaborative environment. &nbsp; Eagerness to learn new technologies and adapt to evolving requirements. &nbsp; RELEVANT EXPERIENCE (preferred but not required): &nbsp; Experience with cloud platforms (e.g., AWS, Azure, Google Cloud Platform) is desirable. &nbsp; Knowledge of basic bioinformatics, genomics, and cancer biology &nbsp; Past research experience in urological oncology, bioinformatics, digital pathology, or relevant fields &nbsp; Research experience with developing AI models such as LLM, vision/time series foundation models.&nbsp; &nbsp; #LI-Hybrid, or #LI-Remote &nbsp;The final salary offered to a successful candidate will be dependent on several factors that may include but are not limited to the type and length of experience within the job, type and length of experience within the industry, education, etc. Base pay is one part of the Total Package that is provided to compensate and recognize employees for their work, and this role may be eligible for additional discretionary bonuses/incentives, and restricted stock units. Veracyte is a multi-state employer, and this salary range may not reflect positions that work in other states.Pay range$101,000&mdash;$140,000 USD&nbsp; What We Can Offer You Veracyte is a growing company that offers significant career opportunities if you are curious, driven, patient-oriented and aspire to help us build a great company. We offer competitive compensation and benefits, and are committed to fostering an inclusive workforce, where diverse backgrounds are represented, engaged, and empowered to drive innovative ideas and decisions. We are thrilled to be recognized as a 2024 Certified™ Great Place to Work® in both the US and Israel - a testament to our dynamic, inclusive, and inspiring workplace where passion meets purpose. &nbsp; About Veracyte Veracyte&nbsp;(Nasdaq: VCYT) is a global genomic diagnostics company that improves patient care by providing answers to clinical questions, informing diagnosis and treatment decisions throughout the patient journey in cancer and other diseases. The company’s growing menu of genomic tests leverage advances in genomic science and technology, enabling patients to avoid risky, costly diagnostic procedures and quicken time to appropriate treatment. The company’s tests in lung cancer, prostate cancer, breast cancer, thyroid cancer, bladder cancer and idiopathic pulmonary fibrosis are available to patients and its lymphoma subtyping and renal cancer tests are in development. With Veracyte’s exclusive global license to a best-in-class diagnostics instrument platform, the company is positioned to deliver its tests to patients worldwide.&nbsp;Veracyte&nbsp;is based in&nbsp;South San Francisco, California. For more information, please visit&nbsp;www.veracyte.com and follow the company on X (Formerly Twitter). Veracyte, Inc. is an Equal Opportunity Employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status or disability status. Veracyte participates in E-Verify in the United States. View our&nbsp;CCPA Disclosure Notice. If you receive any suspicious alerts or communications through LinkedIn or other online job sites for any position at Veracyte, please exercise caution and promptly report any concerns to careers@veracyte.com

Data Scientist II (RWD)

At Veracyte, we offer exciting career opportunities for those interested in joining a pioneering team that is committed to transforming cancer care for patients across the globe. Working at Veracyte enables our employees to not only make a meaningful impact on the lives of patients, but to also learn and grow within a purpose driven&nbsp;environment. This is what we call the Veracyte way&nbsp;– it’s about how we work together, guided by our values, to give clinicians the insights they need to help patients make life-changing decisions.&nbsp; Our Values: We Seek A Better Way: We innovate boldly, learn from our setbacks, and are resilient in our pursuit to transform cancer care We Make It Happen: We act with urgency, commit to quality, and bring fun to our hard work We Are Stronger Together:&nbsp;We collaborate openly, seek to understand, and celebrate our wins We Care Deeply: We embrace our differences, do the right thing, and encourage each other &nbsp;&nbsp; Position Summary Veracyte is seeking an experienced and strategically driven Director of Corporate Communications to lead all external communications efforts for the company. Reporting to the SVP of Corporate Marketing and Communications, this role will shape and deliver our public voice—managing media relations, corporate messaging, executive visibility, and external content strategy. The ideal candidate is both a storyteller and a strategist, capable of crafting compelling narratives, building strong media relationships, and aligning communications with business goals and brand positioning. Key Responsibilities Media Relations &amp; Visibility · Lead proactive media outreach, including development of pitch angles, pitch preparation, delivery, and media relationship development. · Respond to inbound media inquiries, evaluate visibility opportunities, and provide timely, thoughtful responses. · Draft and distribute press releases; ensure alignment with company messaging. · Prepare spokespeople with talking points, briefing materials, and media training as needed. · Monitor media coverage and deliver weekly wrap-up summaries and quarterly editorial recaps with actionable insights. Messaging &amp; Narrative Development · Develop and maintain consistent external messaging frameworks that support corporate narrative, positioning and brand strategy. · Manage and update corporate-level messaging documents, media Q&amp;A libraries, and positioning statements. · Lead development of company-level narratives, storylines, and assets, including copy blocks, FAQs, videos, and web content. · Develop and publish engaging long- and short-form content for corporate social media platforms that align with broader external messaging themes and milestones · Develop content that supports brand visibility and executive voice for social and web. · Work with product teams to ensure product narrative success with media. Strategic Communications Planning · Create and execute corporate public relations strategies, campaigns and themes each year in support of priority business initiatives. · Maintain and drive the corporate external calendar, aligning announcements, events and campaigns with product, commercial, and investor timelines. · Track and amplify major milestones such as scientific publications, conference presentations, and data announcements. · Monitor market messages and communications trends to make recommendations. · Collaborate with product and commercial teams to ensure consistency of message across functions and channels. Reputation &amp; Thought Leadership · Identify and manage corporate award submissions and executive speaking opportunities to elevate visibility and credibility. · Partner with internal stakeholders to define topics, prepare submissions, and coordinate participation in high-impact events. · Partner with HR on recruitment brand · Identify influencers in key areas to cultivate external spokespeople, partners and programs. Governance &amp; Approvals · Route all external-facing materials through appropriate internal review cycles; ensure timely approvals and message integrity. · Manage versions, content routing processes, and documentation of final approved materials. · Maintain the crisis communications framework in partnership with legal and leadership teams. Who You Are · Bachelor’s degree in Communications, Public Relations, Journalism, or a related field; advanced degree a plus. · 10+ years of experience in corporate communications, public relations, or external affairs, preferably in healthcare, diagnostics, biotech, or a regulated industry. · Proven track record in media relations, messaging development, and managing high-impact communications programs. · Exceptional writing, editing, and storytelling skills. · Strong project management and organizational abilities with experience managing multiple initiatives in a matrixed environment. · Comfort working cross-functionally and at all levels of an organization, including with senior leadership. Preferred Experience · Familiarity with press release issuing tools, social media publishing tools, media monitoring platforms (e.g., Cision, Meltwater). · Experience translating scientific or technical content into accessible, high-impact stories. · Background supporting product and brand communications in a fast-paced, innovation-driven environment. &nbsp; To Apply: Please submit your resume, cover letter, and portfolio or writing samples to careers@veracyte.com &nbsp;The final salary offered to a successful candidate will be dependent on several factors that may include but are not limited to the type and length of experience within the job, type and length of experience within the industry, education, etc. Base pay is one part of the Total Package that is provided to compensate and recognize employees for their work, and this role may be eligible for additional discretionary bonuses/incentives, and restricted stock units. Veracyte is a multi-state employer, and this salary range may not reflect positions that work in other states.Pay range$177,000&mdash;$204,000 USD&nbsp; What We Can Offer You Veracyte is a growing company that offers significant career opportunities if you are curious, driven, patient-oriented and aspire to help us build a great company. We offer competitive compensation and benefits, and are committed to fostering an inclusive workforce, where diverse backgrounds are represented, engaged, and empowered to drive innovative ideas and decisions. We are thrilled to be recognized as a 2024 Certified™ Great Place to Work® in both the US and Israel - a testament to our dynamic, inclusive, and inspiring workplace where passion meets purpose. &nbsp; About Veracyte Veracyte&nbsp;(Nasdaq: VCYT) is a global genomic diagnostics company that improves patient care by providing answers to clinical questions, informing diagnosis and treatment decisions throughout the patient journey in cancer and other diseases. The company’s growing menu of genomic tests leverage advances in genomic science and technology, enabling patients to avoid risky, costly diagnostic procedures and quicken time to appropriate treatment. The company’s tests in lung cancer, prostate cancer, breast cancer, thyroid cancer, bladder cancer and idiopathic pulmonary fibrosis are available to patients and its lymphoma subtyping and renal cancer tests are in development. With Veracyte’s exclusive global license to a best-in-class diagnostics instrument platform, the company is positioned to deliver its tests to patients worldwide.&nbsp;Veracyte&nbsp;is based in&nbsp;South San Francisco, California. For more information, please visit&nbsp;www.veracyte.com and follow the company on X (Formerly Twitter). Veracyte, Inc. is an Equal Opportunity Employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status or disability status. Veracyte participates in E-Verify in the United States. View our&nbsp;CCPA Disclosure Notice. If you receive any suspicious alerts or communications through LinkedIn or other online job sites for any position at Veracyte, please exercise caution and promptly report any concerns to careers@veracyte.com

Director, Corporate Communications

At Veracyte, we offer exciting career opportunities for those interested in joining a pioneering team that is committed to transforming cancer care for patients across the globe. Working at Veracyte enables our employees to not only make a meaningful impact on the lives of patients, but to also learn and grow within a purpose driven&nbsp;environment. This is what we call the Veracyte way&nbsp;– it’s about how we work together, guided by our values, to give clinicians the insights they need to help patients make life-changing decisions.&nbsp; Our Values: We Seek A Better Way: We innovate boldly, learn from our setbacks, and are resilient in our pursuit to transform cancer care We Make It Happen: We act with urgency, commit to quality, and bring fun to our hard work We Are Stronger Together:&nbsp;We collaborate openly, seek to understand, and celebrate our wins We Care Deeply: We embrace our differences, do the right thing, and encourage each other &nbsp;The Position: This is a can be a remote or hybrid position. We have office in San Diego and South San Francisco, CA.&nbsp; Based on candidate location, we may consider (PST) remote. We are seeking a highly experienced and collaborative Director Software Quality to lead the testing process for all regulated applications at Veracyte that directly help our company expand and develop new diagnostic solutions to improve patient outcomes and lower healthcare costs. This is a critical role for a technically adept professional who brings deep expertise in enterprise computerized systems, laboratory operations, and scientific data management, particularly in genomics, life sciences, and/or regulated lab environments. As a Director Software Quality, you will serve as a primary owner of testing strategies for software and computerized systems releases, translating complex technical requirements into robust, risk-based scalable testing strategies. You’ll work cross-functionally with software developers, IT teams, and business stakeholders to optimize testing efficiency, data integrity, and compliance. Your contributions will have direct, strategic impact on lab productivity and broader scientific outcomes. Key Responsibilities Act as key point of contact for testing and QA aspects of releases, providing testing services and coordinating with internal resources. Review and approve test cases, scripts, plans and reports (manual and automated) Mentor software quality testers with current CSV methodology. Demonstrated strong analytical skills coupled with the ability to find and solve the root cause of problems. Excellent critical thinking and troubleshooting skills. Serve as a liaison between internal technical teams, and third-party software vendors where applicable Manage and prioritize testing related projects, ensuring timely delivery within scope and with a focus on quality and long-term sustainability. Identify opportunities for continuous improvement and potential automation of testing strategies and processes. Ensure adherence to regulatory and data integrity standards across computerized systems environment. Who You Are: Required: 10+ years of experience in software and/or computerized system LIMS testing, preferably Labbit LIMS or equivalent, with increasing levels of responsibility. Bachelor’s or Master’s degree in Life Sciences, Bioinformatics, Computer Science, or a related field. In-depth understanding of laboratory science workflows, particularly in genomics, molecular biology, or clinical research environments. Proven experience translating technical requirements into risk-based testing strategies. Strong communication and interpersonal skills, with the ability to lead cross-functional discussions. Demonstrated ability to manage complex projects involving multiple stakeholders, with clear timelines and outcomes. Solid understanding of GAMP5 risk based computerized systems validation methodology Solid understanding of regulatory requirements, including GxP, GLP, GCP, CLIA, and data integrity frameworks. Preferred: Familiarity with Agile development methodologies and tools such as Jira and Confluence. &nbsp; #LI-Hybrid,&nbsp; #LI-Remote &nbsp;The final salary offered to a successful candidate will be dependent on several factors that may include but are not limited to the type and length of experience within the job, type and length of experience within the industry, education, etc. Base pay is one part of the Total Package that is provided to compensate and recognize employees for their work, and this role may be eligible for additional discretionary bonuses/incentives, and restricted stock units. Veracyte is a multi-state employer, and this salary range may not reflect positions that work in other states.Pay range$215,000&mdash;$225,000 USD&nbsp; What We Can Offer You Veracyte is a growing company that offers significant career opportunities if you are curious, driven, patient-oriented and aspire to help us build a great company. We offer competitive compensation and benefits, and are committed to fostering an inclusive workforce, where diverse backgrounds are represented, engaged, and empowered to drive innovative ideas and decisions. We are thrilled to be recognized as a 2024 Certified™ Great Place to Work® in both the US and Israel - a testament to our dynamic, inclusive, and inspiring workplace where passion meets purpose. &nbsp; About Veracyte Veracyte&nbsp;(Nasdaq: VCYT) is a global genomic diagnostics company that improves patient care by providing answers to clinical questions, informing diagnosis and treatment decisions throughout the patient journey in cancer and other diseases. The company’s growing menu of genomic tests leverage advances in genomic science and technology, enabling patients to avoid risky, costly diagnostic procedures and quicken time to appropriate treatment. The company’s tests in lung cancer, prostate cancer, breast cancer, thyroid cancer, bladder cancer and idiopathic pulmonary fibrosis are available to patients and its lymphoma subtyping and renal cancer tests are in development. With Veracyte’s exclusive global license to a best-in-class diagnostics instrument platform, the company is positioned to deliver its tests to patients worldwide.&nbsp;Veracyte&nbsp;is based in&nbsp;South San Francisco, California. For more information, please visit&nbsp;www.veracyte.com and follow the company on X (Formerly Twitter). Veracyte, Inc. is an Equal Opportunity Employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status or disability status. Veracyte participates in E-Verify in the United States. View our&nbsp;CCPA Disclosure Notice. If you receive any suspicious alerts or communications through LinkedIn or other online job sites for any position at Veracyte, please exercise caution and promptly report any concerns to careers@veracyte.com

Director Software Quality

At Veracyte, we offer exciting career opportunities for those interested in joining a pioneering team that is committed to transforming cancer care for patients across the globe. Working at Veracyte enables our employees to not only make a meaningful impact on the lives of patients, but to also learn and grow within a purpose driven&nbsp;environment. This is what we call the Veracyte way&nbsp;– it’s about how we work together, guided by our values, to give clinicians the insights they need to help patients make life-changing decisions.&nbsp; Our Values: We Seek A Better Way: We innovate boldly, learn from our setbacks, and are resilient in our pursuit to transform cancer care We Make It Happen: We act with urgency, commit to quality, and bring fun to our hard work We Are Stronger Together:&nbsp;We collaborate openly, seek to understand, and celebrate our wins We Care Deeply: We embrace our differences, do the right thing, and encourage each other &nbsp;The Position: Job Summary and Description: Veracyte is seeking a highly motivated and detail-oriented Equipment Operations Engineer to join our Equipment Engineering and Operations team at our South San Francisco headquarters. The Equipment Operations Engineer is responsible for ensuring reliability, compliance, and operational availability of laboratory equipment across clinical and research environments in adherence to Veracyte’s equipment lifecycle management program. The scope of equipment includes a diverse range of assets such as liquid handlers, spectrophotometers, analyzers, and more.&nbsp; The ideal candidate will bring a collaborative spirit and work cross-functionally with teams in Automation, Product Development, Quality, and Clinical Operations. Depending on level, this role ranges from executing technical tasks under guidance, to driving cross-functional initiatives, to leading complex investigations and mentoring members within the Equipment Engineering and Operations team. This is an on-site, 6-month contract role located in South San Francisco, CA. Responsibilities: Support optimization and adherence to the equipment lifecycle program and processes from procurement, installation, qualification (IQ/OQ/PQ), calibration, and preventive maintenance to decommissioning. Independently manage equipment systems, including internal investigations and service coordination, documentation, and continuous improvement related to equipment performance. Troubleshoot and support root cause investigations for equipment failures and implement correct actions. Support cross-functional efforts related to new equipment onboarding, equipment relocations, obsolescence planning, and lab expansions. Coordinate maintenance, calibration, verification, and qualification activities across internal stakeholders (R&amp;D and CLIA) and external service vendors to minimize impact on lab workflows while ensuring regulatory compliance. Maintain accurate and compliant documentation for all equipment-related activities, support audits, inspections, and internal reviews. Support development of equipment maintenance strategies to minimize downtime and increase overall equipment reliability. Support investigations as SME in NCR’s and CAPA’s as needed. Support development and authoring equipment specifications, user requirements, and IQ/OQ protocols. Support equipment qualification activities. Ensure all equipment and processes meet quality and regulatory standards (CLIA, CAP, IVD, and/or FDA regulations). Adhere to procedures and policies outlined within Veracyte’s quality management system. Who You Are: 2-4 years of related experience with a BS/BA or higher degree in an Engineering field or equivalent work experience. 2-4 years of hands-on experience in equipment engineering or reliability engineering within a highly regulated environment. 2-4 years of experience developing/writing equipment qualification plans, calibration strategies, and maintenance &amp; operation procedures. Familiarity with lab instrumentation, preventive maintenance, and calibration standards. Effective analytical and problem-solving skills with the ability to diagnose complex equipment issues and drive resolution independently or collaboratively. Proficient with common software tools (e.g. Microsoft Office, Google Suite). Strong organizational skills with a keen attention to detail and documentation accuracy. Effective communication and interpersonal skills; ability to work cross-functionally. Excellent time management skills to support a fast-paced working environment. Preferred Qualifications Experience with sequencing assays and automation platforms. Familiarity with CMMS (BMRAM, Limble, EAM, SAP) and LIMS integration. Working knowledge of root cause analysis tools (e.g. 5 whys, fishbone, FMEA) and reliability principles. Experience with Six Sigma principals, SSGB or other reliability certification a significant plus. &nbsp; &nbsp; #LI-Onsite &nbsp;The final salary offered to a successful candidate will be dependent on several factors that may include but are not limited to the type and length of experience within the job, type and length of experience within the industry, education, etc. Base pay is one part of the Total Package that is provided to compensate and recognize employees for their work, and this role may be eligible for additional discretionary bonuses/incentives, and restricted stock units. Veracyte is a multi-state employer, and this salary range may not reflect positions that work in other states.Pay range$46&mdash;$51 USD&nbsp; What We Can Offer You Veracyte is a growing company that offers significant career opportunities if you are curious, driven, patient-oriented and aspire to help us build a great company. We offer competitive compensation and benefits, and are committed to fostering an inclusive workforce, where diverse backgrounds are represented, engaged, and empowered to drive innovative ideas and decisions. We are thrilled to be recognized as a 2024 Certified™ Great Place to Work® in both the US and Israel - a testament to our dynamic, inclusive, and inspiring workplace where passion meets purpose. &nbsp; About Veracyte Veracyte&nbsp;(Nasdaq: VCYT) is a global genomic diagnostics company that improves patient care by providing answers to clinical questions, informing diagnosis and treatment decisions throughout the patient journey in cancer and other diseases. The company’s growing menu of genomic tests leverage advances in genomic science and technology, enabling patients to avoid risky, costly diagnostic procedures and quicken time to appropriate treatment. The company’s tests in lung cancer, prostate cancer, breast cancer, thyroid cancer, bladder cancer and idiopathic pulmonary fibrosis are available to patients and its lymphoma subtyping and renal cancer tests are in development. With Veracyte’s exclusive global license to a best-in-class diagnostics instrument platform, the company is positioned to deliver its tests to patients worldwide.&nbsp;Veracyte&nbsp;is based in&nbsp;South San Francisco, California. For more information, please visit&nbsp;www.veracyte.com and follow the company on X (Formerly Twitter). Veracyte, Inc. is an Equal Opportunity Employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status or disability status. Veracyte participates in E-Verify in the United States. View our&nbsp;CCPA Disclosure Notice. If you receive any suspicious alerts or communications through LinkedIn or other online job sites for any position at Veracyte, please exercise caution and promptly report any concerns to careers@veracyte.com

Equipment Engineering and Operations II

At Veracyte, we offer exciting career opportunities for those interested in joining a pioneering team that is committed to transforming cancer care for patients across the globe. Working at Veracyte enables our employees to not only make a meaningful impact on the lives of patients, but to also learn and grow within a purpose driven&nbsp;environment. This is what we call the Veracyte way&nbsp;– it’s about how we work together, guided by our values, to give clinicians the insights they need to help patients make life-changing decisions.&nbsp; Our Values: We Seek A Better Way: We innovate boldly, learn from our setbacks, and are resilient in our pursuit to transform cancer care We Make It Happen: We act with urgency, commit to quality, and bring fun to our hard work We Are Stronger Together:&nbsp;We collaborate openly, seek to understand, and celebrate our wins We Care Deeply: We embrace our differences, do the right thing, and encourage each other &nbsp;The Position: Job Summary and Description: Veracyte is seeking a highly motivated and detail-oriented Equipment Operations Engineer to join our Equipment Engineering and Operations team at our South San Francisco headquarters. The Equipment Operations Engineer is responsible for ensuring reliability, compliance, and operational availability of laboratory equipment across clinical and research environments in adherence to Veracyte’s equipment lifecycle management program. The scope of equipment includes a diverse range of assets such as liquid handlers, spectrophotometers, analyzers, and more.&nbsp; The ideal candidate will bring a collaborative spirit and work cross-functionally with teams in Automation, Product Development, Quality, and Clinical Operations. Depending on level, this role ranges from executing technical tasks under guidance, to driving cross-functional initiatives, to leading complex investigations and mentoring members within the Equipment Engineering and Operations team. This is an full-time, on-site role located in South San Francisco, CA. Responsibilities: Support optimization and adherence to the equipment lifecycle program and processes from procurement, installation, qualification (IQ/OQ/PQ), calibration, and preventive maintenance to decommissioning. Independently manage equipment systems, including internal investigations and service coordination, documentation, and continuous improvement related to equipment performance. Troubleshoot and support root cause investigations for equipment failures and implement correct actions. Support cross-functional efforts related to new equipment onboarding, equipment relocations, obsolescence planning, and lab expansions. Coordinate maintenance, calibration, verification, and qualification activities across internal stakeholders (R&amp;D and CLIA) and external service vendors to minimize impact on lab workflows while ensuring regulatory compliance. Maintain accurate and compliant documentation for all equipment-related activities, support audits, inspections, and internal reviews. Support development of equipment maintenance strategies to minimize downtime and increase overall equipment reliability. Support investigations as SME in NCR’s and CAPA’s as needed. Support development and authoring equipment specifications, user requirements, and IQ/OQ protocols. Support equipment qualification activities. Ensure all equipment and processes meet quality and regulatory standards (CLIA, CAP, IVD, and/or FDA regulations). Adhere to procedures and policies outlined within Veracyte’s quality management system. Who You Are: 4-6 years of related experience with a BS/BA or higher degree (2-4 yrs with a Masters Degree) in an Engineering field or equivalent work experience. 4-6 years of hands-on experience in equipment engineering or reliability engineering within a highly regulated environment. 4-6 years of experience developing/writing equipment qualification plans, calibration strategies, and maintenance &amp; operation procedures. Familiarity with lab instrumentation, preventive maintenance, and calibration standards. Effective analytical and problem-solving skills with the ability to diagnose complex equipment issues and drive resolution independently or collaboratively. Proficient with common software tools (e.g. Microsoft Office, Google Suite). Strong organizational skills with a keen attention to detail and documentation accuracy. Effective communication and interpersonal skills; ability to work cross-functionally. Excellent time management skills to support a fast-paced working environment. Preferred Qualifications Experience with sequencing assays and automation platforms. Familiarity with CMMS (BMRAM, Limble, EAM, SAP) and LIMS integration. Working knowledge of root cause analysis tools (e.g. 5 whys, fishbone, FMEA) and reliability principles. Experience with Six Sigma principals, SSGB or other reliability certification a significant plus. &nbsp; &nbsp; #LI-Onsite &nbsp;The final salary offered to a successful candidate will be dependent on several factors that may include but are not limited to the type and length of experience within the job, type and length of experience within the industry, education, etc. Base pay is one part of the Total Package that is provided to compensate and recognize employees for their work, and this role may be eligible for additional discretionary bonuses/incentives, and restricted stock units. Veracyte is a multi-state employer, and this salary range may not reflect positions that work in other states.Pay range$46&mdash;$51 USD&nbsp; What We Can Offer You Veracyte is a growing company that offers significant career opportunities if you are curious, driven, patient-oriented and aspire to help us build a great company. We offer competitive compensation and benefits, and are committed to fostering an inclusive workforce, where diverse backgrounds are represented, engaged, and empowered to drive innovative ideas and decisions. We are thrilled to be recognized as a 2024 Certified™ Great Place to Work® in both the US and Israel - a testament to our dynamic, inclusive, and inspiring workplace where passion meets purpose. &nbsp; About Veracyte Veracyte&nbsp;(Nasdaq: VCYT) is a global genomic diagnostics company that improves patient care by providing answers to clinical questions, informing diagnosis and treatment decisions throughout the patient journey in cancer and other diseases. The company’s growing menu of genomic tests leverage advances in genomic science and technology, enabling patients to avoid risky, costly diagnostic procedures and quicken time to appropriate treatment. The company’s tests in lung cancer, prostate cancer, breast cancer, thyroid cancer, bladder cancer and idiopathic pulmonary fibrosis are available to patients and its lymphoma subtyping and renal cancer tests are in development. With Veracyte’s exclusive global license to a best-in-class diagnostics instrument platform, the company is positioned to deliver its tests to patients worldwide.&nbsp;Veracyte&nbsp;is based in&nbsp;South San Francisco, California. For more information, please visit&nbsp;www.veracyte.com and follow the company on X (Formerly Twitter). Veracyte, Inc. is an Equal Opportunity Employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status or disability status. Veracyte participates in E-Verify in the United States. View our&nbsp;CCPA Disclosure Notice. If you receive any suspicious alerts or communications through LinkedIn or other online job sites for any position at Veracyte, please exercise caution and promptly report any concerns to careers@veracyte.com

Equipment Engineering and Operations III

At Veracyte, we offer exciting career opportunities for those interested in joining a pioneering team that is committed to transforming cancer care for patients across the globe. Working at Veracyte enables our employees to not only make a meaningful impact on the lives of patients, but to also learn and grow within a purpose driven&nbsp;environment. This is what we call the Veracyte way&nbsp;– it’s about how we work together, guided by our values, to give clinicians the insights they need to help patients make life-changing decisions.&nbsp; Our Values: We Seek A Better Way: We innovate boldly, learn from our setbacks, and are resilient in our pursuit to transform cancer care We Make It Happen: We act with urgency, commit to quality, and bring fun to our hard work We Are Stronger Together:&nbsp;We collaborate openly, seek to understand, and celebrate our wins We Care Deeply: We embrace our differences, do the right thing, and encourage each other &nbsp;&nbsp; Job Description: Veracyte is seeking a highly motivated Equipment Operations Associate to join our Equipment Engineering and Operations team at our South San Francisco headquarters.&nbsp;The Equipment Operations Associate’s primary responsibility is to provide support in the equipment lifecycle and maintenance/metrology program. Working under supervision, this entry-level position is responsible for assisting in the coordination, execution, and documentation of equipment-related activities.&nbsp;The ideal candidate will be detail-oriented, collaborative, and eager to learn foundational skills needed to grow within the Equipment Engineering discipline. Location: This is an onsite position based out of our South San Francisco location Responsibilities: Assist in the coordination, scheduling and/or execution of equipment preventive maintenance, calibrations, verifications, and qualifications to ensure minimal disruption to lab operations and ensure compliance with manufacturer specifications and regulatory standards. Participate in the installation, relocation, and decommissioning of lab instruments under the guidance of senior engineers. Support tracking and documentation of equipment service events, calibration records, and qualifications in compliance with regulatory standards (CLIA, CAP, IVD, and/or RDA regulations). Collaborate with internal stakeholders (including R&amp;D and Clinical teams) and external vendors to facilitate timely and efficient service activities. Support troubleshooting and root cause investigations of equipment failures while escalating equipment issues or deviations as needed. Adhere to procedures and policies outlined within Veracyte’s quality management system. Who You Are: High school diploma required. Associate’s or BS/BA in Engineering field preferred. 0-2 years of relevant experience in a laboratory or regulated environment (internship experience accepted). Basic understanding of laboratory instrumentation and preventive maintenance concepts. Strong organizational skills with a keen attention to detail and documentation accuracy. Effective communication and interpersonal skills; ability to work cross-functionally. Proficient with common software tools (e.g. Microsoft Office, Google Suite). Preferred Qualifications: Experience with CMMS, LIMS, or equipment tracking tools. Working knowledge of root cause analysis tools (e.g. 5 whys, fishbone, FMEA). &nbsp; #LI-Onsite &nbsp;The final salary offered to a successful candidate will be dependent on several factors that may include but are not limited to the type and length of experience within the job, type and length of experience within the industry, education, etc. Base pay is one part of the Total Package that is provided to compensate and recognize employees for their work, and this role may be eligible for additional discretionary bonuses/incentives, and restricted stock units. Veracyte is a multi-state employer, and this salary range may not reflect positions that work in other states.Pay range$20&mdash;$23 USD&nbsp; What We Can Offer You Veracyte is a growing company that offers significant career opportunities if you are curious, driven, patient-oriented and aspire to help us build a great company. We offer competitive compensation and benefits, and are committed to fostering an inclusive workforce, where diverse backgrounds are represented, engaged, and empowered to drive innovative ideas and decisions. We are thrilled to be recognized as a 2024 Certified™ Great Place to Work® in both the US and Israel - a testament to our dynamic, inclusive, and inspiring workplace where passion meets purpose. &nbsp; About Veracyte Veracyte&nbsp;(Nasdaq: VCYT) is a global genomic diagnostics company that improves patient care by providing answers to clinical questions, informing diagnosis and treatment decisions throughout the patient journey in cancer and other diseases. The company’s growing menu of genomic tests leverage advances in genomic science and technology, enabling patients to avoid risky, costly diagnostic procedures and quicken time to appropriate treatment. The company’s tests in lung cancer, prostate cancer, breast cancer, thyroid cancer, bladder cancer and idiopathic pulmonary fibrosis are available to patients and its lymphoma subtyping and renal cancer tests are in development. With Veracyte’s exclusive global license to a best-in-class diagnostics instrument platform, the company is positioned to deliver its tests to patients worldwide.&nbsp;Veracyte&nbsp;is based in&nbsp;South San Francisco, California. For more information, please visit&nbsp;www.veracyte.com and follow the company on X (Formerly Twitter). Veracyte, Inc. is an Equal Opportunity Employer and will consider all qualified applicants for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status or disability status. Veracyte participates in E-Verify in the United States. View our&nbsp;CCPA Disclosure Notice. If you receive any suspicious alerts or communications through LinkedIn or other online job sites for any position at Veracyte, please exercise caution and promptly report any concerns to careers@veracyte.com

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