Mineralys Therapeutics is a biotechnology company dedicated to advancing innovative therapies for various medical conditions. Founded on a mission to revolutionize the field of medicine, Mineralys Therapeutics is committed to developing cutting-edge treatments that address unmet medical needs and improve patient outcomes. With a focus on research and development, the company is at the forefront of discovering novel therapeutic approaches that have the potential to transform healthcare.

&nbsp; Mineralys Therapeutics is a publicly traded, clinical-stage biotechnology company focused on developing medicines to target diseases driven by abnormally elevated aldosterone. Our initial product candidate, lorundrostat, is a proprietary, orally administered, highly selective aldosterone synthase inhibitor that we are developing for cardiorenal conditions affected by abnormally elevated aldosterone, including hypertension and chronic kidney disease. Mineralys is a fully remote company. For more information, please visit&nbsp;https://mineralystx.com. Follow Mineralys on&nbsp;LinkedIn. The SharePoint Administrator will manage and maintain our SharePoint Online and on-premises environments and will report into the VP, IT. The ideal candidate will have strong expertise in SharePoint administration, governance, and security, with a strong focus on information architecture and content organization. This role will ensure our SharePoint platform remains secure, well-structured, and optimized for collaboration across the business. Responsibilities&nbsp; Administer and maintain SharePoint Online and SharePoint Server environments, including site collections, subsites, permissions, and governance.&nbsp; Manage and configure document libraries, records management, and metadata-driven information architecture (content types, columns, and term stores).&nbsp; Implement and enforce document tagging and taxonomy standards to improve searchability, compliance, and user adoption.&nbsp; Oversee user and group permissions, security policies, and external sharing configurations in alignment with organizational compliance standards.&nbsp; Support and monitor system performance, usage analytics, and troubleshoot issues across the tenant.&nbsp; Configure site templates and build re-usable Web Parts.&nbsp; Automate administrative tasks using PowerShell (including PnP.PowerShell) for provisioning, reporting, and configuration.&nbsp; Assist with migration projects from on-premises or legacy platforms to SharePoint Online, ensuring proper metadata mapping and retention.&nbsp; Collaborate with business stakeholders to gather requirements, provide end-user support, training, and document best practices.&nbsp; Core Competencies&nbsp; Strong expertise in SharePoint Online administration. Proven experience with document tagging, metadata management, content types, and taxonomy/term store configuration.&nbsp; Experience with SPFx. Knowledge of sensitivity labels and record retention. Proficiency in PowerShell scripting for automation and tenant reporting. Knowledge of Microsoft 365 ecosystem (Teams, OneDrive, Exchange) and its integration with SharePoint. Familiarity with Azure Active Directory (Entra ID), MFA, and security administration.&nbsp; Understanding of compliance, governance, and lifecycle management for documents and records Demonstrate Our Core Values&nbsp; Velocity – Drive Speed with Purpose Foresight &amp; Acceleration Execution Under Tight Timelines Clear Decision-Making in Ambiguity Data-Driven Decision Making – Ground Strategy in Evidence Subject Matter Intelligence &amp; Precedent-Based Reasoning Data Interpretation Metrics-Oriented Agile Mindset – Embrace Iteration and Change Adaptability to Shifting Development Plans Iterative Planning &amp; Engagement Frictionless Execution – Simplify the Path to Results Operational Clarity &amp; Precision Lean, Cross-Functional Collaboration Strategic Communication Autonomy – Lead with Ownership and Accountability Self-Directed and Proactive Trusted Decision Maker Leads from the Front Execution that Delivers Value Define success up front Follow through with discipline Deliver results that move the business Qualifications&nbsp; Minimum of 5 years of experience in a similar role. Experience with SharePoint Advanced Management features.&nbsp; Familiarity with Power Platform (Power Automate, Power Apps) for enhancing workflows.&nbsp; Knowledge of search configuration and optimization using metadata.&nbsp; Strong communication and documentation skills for end-user guidance and governance standards.&nbsp; &nbsp;Travel: Requires minimal domestic travel.&nbsp; This position is eligible for standard Company benefits including medical, dental, vision, time off and 401K, as well as participating in Mineralys incentive plans are contingent on achievement of personal and company performance. Actual compensation may vary from posted hiring range based on geographic location, work experience, education, and/or skill level. US Salary Range: $105,000 - $120,000 #LI-Remote &nbsp;

SharePoint Administrator

Mineralys Therapeutics is a publicly traded, clinical-stage biotechnology company focused on developing medicines to target diseases driven by abnormally elevated aldosterone. Our initial product candidate, lorundrostat, is a proprietary, orally administered, highly selective aldosterone synthase inhibitor that we are developing for cardiorenal conditions affected by abnormally elevated aldosterone, including hypertension and chronic kidney disease. Mineralys is a fully remote company. For more information, please visit&nbsp;https://mineralystx.com. Follow Mineralys on&nbsp;LinkedIn. Reporting to the VP of Marketing, the Director, Consumer and Patient Marketing will be responsible for defining and implementing consumer and patient brand strategy to drive brand awareness and shape a positive patient experience. This position will play a critical role in the launch success through creative and impactful DTC/DTP initiatives. This role is perfect for someone who thrives in an entrepreneurial setting and is excited to shape a brand from day one. Principal Responsibilities Define the consumer and patient brand strategy, including patient journey, positioning, segmentation, and messaging Partner with market research to identify actionable patient insights to drive innovation and ideation in DTC and DTP strategies. Lead creative and digital agencies to develop out of the box, high-impact, multichannel consumer and patient campaigns. Oversee the development of unbranded and branded patient education materials, support programs, and engagement tools. Collaborate with Market Access to design innovative patient support programs to support patient onboarding, adherence, and retention. Work closely with internal teams (Medical, Legal, Regulatory, Compliance) to ensure compliant and aligned messaging Evaluate the effectiveness of promotional strategies through campaign measurement and metrics development to ensure positive return on investment and achievement of brand objectives. Skills and Attributes Flexibility to adapt to a fast-changing, ambiguous environment in an organization without fully established procedures Velocity – Drive Speed with Purpose Foresight &amp; Acceleration Execution Under Tight Timelines Clear Decision-Making in Ambiguity Data-Driven Decision Making – Ground Strategy in Evidence Subject Matter Intelligence &amp; Precedent-Based Reasoning Data Interpretation Metrics-Oriented Agile Mindset – Embrace Iteration and Change Adaptability to Shifting Development Plans Iterative Planning &amp; Engagement Frictionless Execution – Simplify the Path to Results Operational Clarity &amp; Precision Lean, Cross-Functional Collaboration Strategic Communication Autonomy – Lead with Ownership and Accountability Self-Directed and Proactive Trusted Decision Maker Leads from the Front Execution that Delivers Value Define success up front Follow through with discipline Deliver results that move the business Travel This position requires up to 20 % travel. &nbsp;Frequently travel is outside the local area and overnight. Some of the travel may be international. &nbsp;Education and Experience MBA or bachelor’s degree plus 8+ years of pharmaceutical or biotech industry experience with at least 5 years building and executing marketing strategies &nbsp; DTC and launch experience is strongly preferred Cardiovascular experience is preferred. Demonstrated ability to develop and execute consumer/patient brand strategy and bring new thinking to promotional campaigns Strong project management skills, with the ability to manage multiple priorities and stakeholders. Experience leading cross-functional teams and agency partners. A self-starter mindset with high personal accountability, resourcefulness, and a collaborative spirit. Excellent communication and presentation skills. These positions are eligible for standard Company benefits including medical, dental, vision, time off and 401K, as well as participating in Mineralys incentive plans are contingent on achievement of personal and company performance. Actual compensation may vary from posted hiring range based on geographic location, work experience, education, and/or skill level. US Salary Range:&nbsp; $175,000 - $195,000 #LI-Remote &nbsp; &nbsp; &nbsp;

Director, Consumer & Patient Marketing

Mineralys Therapeutics is a publicly traded, clinical-stage biotechnology company focused on developing medicines to target diseases driven by abnormally elevated aldosterone. Our initial product candidate, lorundrostat, is a proprietary, orally administered, highly selective aldosterone synthase inhibitor that we are developing for cardiorenal conditions affected by abnormally elevated aldosterone, including hypertension and chronic kidney disease. Mineralys is a fully remote company. For more information, please visit&nbsp;https://mineralystx.com. Follow Mineralys on&nbsp;LinkedIn. We are seeking a highly strategic and analytical Director of Market Access to lead the development of the value proposition, evidence generation, pricing, and contracting strategy for the launch of a novel cardiovascular therapy. This is a role focused on shaping payer strategy and cross-functional alignment to ensure optimal access and reimbursement readiness at launch. Key Responsibilities Value Proposition Development Lead the creation of a compelling, data-driven value proposition tailored to payer and policy stakeholder needs Collaborate with Medical Affairs, HEOR, and Clinical teams to align messaging with product profile and unmet need Develop payer-facing materials including AMCP dossiers, PIE and value decks Evidence Generation Strategy Identify any evidence gaps and prioritize evidence needs to support access and reimbursement goals Partner with HEOR and RWE teams to guide development of economic models, burden-of-illness studies, and comparative effectiveness research Pricing &amp; Contracting Strategy Develop pricing scenarios and recommendations based on market dynamics, competitive intelligence, and value frameworks Design innovative contracting approaches (e.g., value-based agreements, outcomes-based models) in collaboration with internal stakeholders Ensure alignment with legal, regulatory, and compliance teams on contract structures and risk mitigation Cross-Functional Leadership Serve as the internal market access lead for the cardiovascular launch team Provide strategic input to Commercial, Medical, Regulatory, and Finance teams to ensure access readiness Policy &amp; Landscape Monitoring Stay abreast of evolving reimbursement policies, HTA trends, and payer expectations in cardiovascular care Translate external insights into actionable internal strategies Qualifications&nbsp; 10+ years of experience in market access, pricing, HEOR, or strategy roles within the pharmaceutical industry Demonstrated success in developing access strategies for specialty or cardiovascular products Strong understanding of U.S. payer systems, reimbursement pathways, and value demonstration frameworks Exceptional analytical, strategic thinking, and communication skills Advanced degree preferred (MBA, MPH, PharmD, or equivalent) Demonstrated ability to operate effectively in ambiguous, fast-changing environments, with a proactive and solution-oriented mindset These positions are eligible for standard Company benefits including medical, dental, vision, time off and 401K, as well as participating in Mineralys incentive plans are contingent on achievement of personal and company performance. Actual compensation may vary from posted hiring range based on geographic location, work experience, education, and/or skill level. US Salary Range:&nbsp; $210,000 - $240,000 #LI-Remote &nbsp; &nbsp; &nbsp;

Director, Market Access

&nbsp; Mineralys Therapeutics is a publicly traded, clinical-stage biotechnology company focused on developing medicines to target diseases driven by abnormally elevated aldosterone. Our initial product candidate, lorundrostat, is a proprietary, orally administered, highly selective aldosterone synthase inhibitor that we are developing for cardiorenal conditions affected by abnormally elevated aldosterone, including hypertension and chronic kidney disease. Mineralys is a fully remote company. For more information, please visit&nbsp;https://mineralystx.com. Follow Mineralys on&nbsp;LinkedIn. &nbsp; The Director, Medical Value &amp; Outcomes functions as a highly trained, field-based, scientific expert who engages health care professionals and external experts in the exchange of clinical, scientific, and research information on one or more of Mineralys’ products. The Director, MVO is responsible for establishing, cultivating, and maintaining professional relationships with key stakeholders, including healthcare professionals (HCPs), Medical Thought Leaders, Payors and Managed Care Organizations, Government Employees, etc. The Director, MVO works closely with the Market Access team to engage payors and Key Decision Makers. These interactions will be conducted in a compliant manner and in accordance with all local, state, and national regulations and guidelines.&nbsp; The Director, MVO functions as a part of the medical affairs team and cross-function collaborator to provide product and pipeline therapeutic area expertise to payors and other HCP stakeholders. The Director, MVO collects key insights and serves as a scientific partner and subject matter expert to internal colleagues and stakeholders. Position Responsibilities Functions as the primary subject matter expert for Mineralys Medical Affairs and Market Access Teams to provide product and pipeline therapeutic area expertise Contribute scientific and medical support for the Market Access team, in alignment with corporate objectives. Identify, establish, and develop relationships with key population health decision makers &nbsp;and work closely with the Market Access team to engage these payors and other key decision makers while developing a strong understanding of territory specific healthcare systems and payor practices. Works closely with the Market Access team to serve as a scientific resource at payor accounts and integrated delivery networks when requested Develop a tactical customer-centric medical engagement plan in alignment with management Provides timely clinical, economic, and scientific product updates proactively or in response to unsolicited requests per standard operating procedure (including Dossiers) to formulary decision makers or similar entities Knowledgeable regarding role of value evidence as used by payor decision makers to inform adoption and diffusion decisions Covers select Congresses with the expectations of attending sessions, managing the medical information booth, hosting debriefs, and providing executive summary to the appropriate members of the leadership and cross-functional team Ensure policies, procedures, and guidance are adhered to and perform all Company business in accordance with all regulations (e.g. EEO FDA, OSHA, PDMA, EPA PhRMA, etc.) &nbsp; Education, Experience &amp; Skill Requirements Advanced degree in the scientific discipline required (MD, PhD, PharmD, NP/PA, MSN with direct payor experience, MSL experience with Health Economics and Outcomes Research (HEOR) experience, or a related field) 7+ years of experience required in pharmaceutical industry in roles such as: Medical Value, Health Outcomes, Field HEOR, or similar field-based payer liaison roles (direct payer health plan experience is a plus) Knowledge of regional-specific and national healthcare systems, HEOR, and payors. Deep understanding of US healthcare industry trends, and in-depth knowledge of the US healthcare delivery system, including payors and organized providers and ability to apply this understanding in support of field-based activities Ability to translate data-driven evidence into decisions, discussions, and actions that align to customer needs Strong business acumen with proven ability to apply health outcomes programs or research findings to impact market access decisions Deep understanding of scientific, clinical, market, and product information and the ability to discuss and communicate this information with top experts in their field. Experience in a small biotechnology or pharmaceutical environment is preferred. Superior written and oral communication skills &nbsp;Travel: Must be located within driving distance of a major international airport; approx. 50% travel. Valid US driver’s license required, ability to travel without restrictions. This position is eligible for standard Company benefits including medical, dental, vision, time off and 401K, as well as participating in Mineralys incentive plans are contingent on achievement of personal and company performance. Actual compensation may vary from posted hiring range based on geographic location, work experience, education, and/or skill level. US Salary Range:&nbsp; $228,000 - $244,000 #LI-remote &nbsp;

Director, Medical Value & Outcomes

&nbsp; Mineralys Therapeutics is a publicly traded, clinical-stage biotechnology company focused on developing medicines to target diseases driven by abnormally elevated aldosterone. Our initial product candidate, lorundrostat, is a proprietary, orally administered, highly selective aldosterone synthase inhibitor that we are developing for cardiorenal conditions affected by abnormally elevated aldosterone, including hypertension and chronic kidney disease. Mineralys is a fully remote company. For more information, please visit&nbsp;https://mineralystx.com. Follow Mineralys on&nbsp;LinkedIn. The Director of Scientific Communications and Engagement is a key partner in the development and implementation of medical communications, congress planning, external scientific engagement, Key Opinion Leader (KOL) engagement strategies, and tactical execution in support of Mineralys Therapeutics’ portfolio. This role will shape how Medical Affairs at Mineralys engages with the medical community, including scientific leaders, professional societies, advocacy groups, and healthcare providers, by driving best-in-class medical education, publications, and omni-channel platforms.&nbsp; &nbsp;This is a unique opportunity to build and scale the function in a dynamic biotech environment, working cross-functionally across departments to ensure that our scientific story is disseminated with accuracy, impact, and credibility.&nbsp; &nbsp; Responsibilities&nbsp; &nbsp;Scientific Communications &amp; Content&nbsp; Lead the development of disease-state and product-specific materials (e.g., slide decks, digital tools, publication extenders) in collaboration with vendors and internal stakeholders.&nbsp; Ensure the Scientific Communication Platform aligns with Medical Communications objectives through cross-functional collaboration.&nbsp; Drive the omni-channel scientific communications strategy in alignment with Medical Affairs and corporate objectives.&nbsp; Develop and implement publication plans to support scientific visibility and credibility.&nbsp; Stay current on evolving medical communications trends, best practices, and channels to deliver impactful and compliant programs.&nbsp; &nbsp;Congress &amp; External Engagement&nbsp; Develop and execute the medical congress strategy, collaborating with Medical Affairs and Clinical Development to ensure an impactful presence at priority meetings.&nbsp; Build and strengthen partnerships with professional societies, advocacy groups, and physician organizations to enhance Mineralys’ scientific visibility and reputation.&nbsp; Identify and cultivate relationships with guideline committee members, KOLs, and other scientific leaders through targeted engagement strategies and relationship management.&nbsp;&nbsp; Strategic Planning &amp; Operations&nbsp; Develop and manage the annual Medical Communications &amp; Information tactical plan, including budget oversight and vendor management.&nbsp; Foster cross-functional collaboration across Medical Affairs, Clinical Development, Program Management, Corporate Communications, and Commercial teams to ensure alignment on strategy and execution.&nbsp; Proactively identify opportunities to expand scientific engagement and education initiatives.&nbsp; Medical Information&nbsp;&nbsp; Oversee the development of standard and custom responses to unsolicited requests, ensuring all content is scientifically accurate, balanced, and compliant.&nbsp; Create and maintain internal Medical Information resources (e.g., FAQs, technical response documents) to support field-based and internal colleagues.&nbsp; Core Competencies&nbsp; Strategic thinker with the ability to translate scientific insights into clear, compelling communications.&nbsp; Strong leadership and cross-functional collaboration skills, with a focus on fostering empowerment and accountability.&nbsp; Demonstrates ability to establish new departmental capabilities, processes, and procedures.&nbsp; Proven strength in project management, consistently delivering multiple workstreams on time and with quality.&nbsp; Highly effective communicator with excellent presentation, writing, and interpersonal skills.&nbsp; Results-driven, proactive problem solver with experience in conflict resolution and vendor management.&nbsp; Qualifications&nbsp; Advanced medical or scientific degree required: MD, PharmD, or PhD.&nbsp; 10+ years of pharmaceutical/biotech Medical Affairs experience, including 5+ years in Medical Communications.&nbsp; Demonstrated success in product launch planning and execution.&nbsp; Experience in publications, congress planning, medical education, and omni-channel content strategy.&nbsp; Established track record of KOL and society engagement as well as scientific collaboration.&nbsp; Strong understanding of regulatory and compliance frameworks governing medical communications (e.g., FDA, OIG, PhRMA, and international equivalents).&nbsp; Proven ability to establish and manage a Medical Information function, including vendor oversight and call center management (preferred).&nbsp; &nbsp;Travel: Up to 30% domestic travel, Valid US driver’s license required, ability to travel without restrictions. This position is eligible for standard Company benefits including medical, dental, vision, time off and 401K, as well as participating in Mineralys incentive plans are contingent on achievement of personal and company performance. Actual compensation may vary from posted hiring range based on geographic location, work experience, education, and/or skill level. US Salary Range:&nbsp; $214,776 - $230,813 #LI-Remote &nbsp;

Director, Scientific Communications & Engagement

Mineralys Therapeutics is a publicly traded, clinical-stage biotechnology company focused on developing medicines to target diseases driven by abnormally elevated aldosterone. Our initial product candidate, lorundrostat, is a proprietary, orally administered, highly selective aldosterone synthase inhibitor that we are developing for cardiorenal conditions affected by abnormally elevated aldosterone, including hypertension and chronic kidney disease. Mineralys is a fully remote company. For more information, please visit&nbsp;https://mineralystx.com. Follow Mineralys on&nbsp;LinkedIn. Reporting to the Senior Vice President Market Access, the Director/Sr. Director of Trade and Distribution will be responsible for developing and implementing strategies for trade, distribution, and channel access.&nbsp;&nbsp; &nbsp;Responsibilities Trade Strategy Development Design and execute the trade and distribution strategy for the cardiovascular antihypertensive product across retail, specialty, and institutional channels. Develop pricing, contracting, and channel access strategies in alignment with brand goals and market dynamics. Channel Strategy Own end-to-end U.S. trade and distribution launch execution for the asset. Establish and manage relationships with 3PL, wholesalers, distributors and GPOs Negotiate and manage contracts with channel partners Oversee implementation and performance of channel partners, ensuring service level agreements and KPIs are met Ensure seamless cross-functional alignment with Brand, Market Access, Supply Chain, Patient Support Services (PSS), and Medical Affairs for launch delivery. Launch Execution Lead cross-functional launch readiness activities related to trade and distribution Ensure product availability across all channels at launch and beyond, minimizing supply disruptions. Performance Monitoring Track and analyze channel performance, inventory levels, and product movement. Develop KPIs and dashboards to monitor trade effectiveness and identify optimization opportunities. Cross-Functional Collaboration Partner with Market Access, Supply Chain, Finance, Regulatory, and Commercial teams to align distribution strategy with broader business objectives. Serve as the internal subject matter expert on trade and distribution. Compliance &amp; Risk Management Ensure adherence to all federal and state regulations including DSCSA, PDMA, and other relevant laws. Implement robust controls to mitigate diversion, counterfeiting, and other supply chain risks. Requirements: Bachelor’s degree required, MBA or advanced degree in business, health sciences, or related field preferred 10+ years of pharmaceutical/biotech experience, with at least 5 years in trade, distribution, or channel strategy Proven track record in leading trade launch readiness and channel execution across both specialty and traditional product categories. Strong background in contract negotiation, vendor management, and cross-functional leadership Excellent communication, negotiation, and relationship management skills to achieve objectives Strong analytical and project management capabilities Proficiency in interpreting and leveraging trade data and performance metrics Efficient independent worker with ability to focus and drive for results Ability to work in a fast-paced environment and to handle multiple tasks Willingness to travel ~30% to meet with trade partners, vendors, attend internal meetings, and represent the company at relevant conventions and events These positions are eligible for standard Company benefits including medical, dental, vision, time off and 401K, as well as participating in Mineralys incentive plans are contingent on achievement of personal and company performance. Actual compensation may vary from posted hiring range based on geographic location, work experience, education, and/or skill level. US Salary Range: $210,000 - $260,000 #LI-Remote &nbsp; &nbsp; &nbsp;

Director/Sr. Director, Commercial Trade and Distribution

Mineralys Therapeutics is a publicly traded, clinical-stage biotechnology company focused on developing medicines to target diseases driven by abnormally elevated aldosterone. Our initial product candidate, lorundrostat, is a proprietary, orally administered, highly selective aldosterone synthase inhibitor that we are developing for cardiorenal conditions affected by abnormally elevated aldosterone, including hypertension and chronic kidney disease. Mineralys is a fully remote company. For more information, please visit&nbsp;https://mineralystx.com. Follow Mineralys on&nbsp;LinkedIn. Reporting to the VP of Marketing, the Director/ Sr. Director, HCP Marketing will lead healthcare professional brand strategy and develop go-to-market launch initiatives to achieve launch success.&nbsp; The ideal candidate will be a self-starter with deep experience in HCP marketing, including launch planning, messaging and creative development, and cross-functional leadership. Previous launch leadership and cardiovascular experience is strongly preferred. This role is perfect for someone who thrives in an entrepreneurial setting and is excited to shape a brand from day one. Principal Responsibilities Lead the development of HCP brand strategy and activation, including positioning, messaging, and tactical plans. Oversee creation and execution of a compelling creative campaign and HCP promotional assets. Partner on HCP focused market research efforts to ensure decisions are well-informed and driven by customer insights to accelerate brand growth and engagement. Serve as the brand lead and primary point person for launch planning, ensuring cross-functional alignment and aligned launch metrics. Work closely with internal teams (Medical, Legal, Regulatory, Compliance) to ensure compliant and aligned messaging Manage relationships with external vendors and agency partners Partner with Sales, Sales Training, and Commercial Operations to develop and optimize field force initiatives to support brand messaging and engagement. Evaluate the effectiveness of promotional strategies through campaign measurement and metrics development to ensure positive return on investment and achievement of brand objectives. Skills and Attributes Flexibility to adapt to a fast-changing, ambiguous environment in an organization without fully established procedures Velocity – Drive Speed with Purpose Foresight &amp; Acceleration Execution Under Tight Timelines Clear Decision-Making in Ambiguity Data-Driven Decision Making – Ground Strategy in Evidence Subject Matter Intelligence &amp; Precedent-Based Reasoning Data Interpretation Metrics-Oriented Agile Mindset – Embrace Iteration and Change Adaptability to Shifting Development Plans Iterative Planning &amp; Engagement Frictionless Execution – Simplify the Path to Results Operational Clarity &amp; Precision Lean, Cross-Functional Collaboration Strategic Communication Autonomy – Lead with Ownership and Accountability Self-Directed and Proactive Trusted Decision Maker Leads from the Front Execution that Delivers Value Define success up front Follow through with discipline Deliver results that move the business Travel &nbsp;This position requires up to 20 % travel. &nbsp;Frequently travel is outside the local area and overnight. Some of the travel may be international. Education and Experience &nbsp;MBA or bachelor’s degree plus 8+ years of pharmaceutical or biotech industry experience with at least 5 years building and executing marketing strategies &nbsp; Launch experience and commercialization of new products preferred Cardiovascular experience is highly preferred. Demonstrated ability to develop and execute brand strategy and promotional campaigns in a fast-paced environment. Strong project management skills, with the ability to manage multiple priorities and stakeholders. Experience leading cross-functional teams and agency partners. A self-starter mindset with high personal accountability, resourcefulness, and a collaborative spirit. Excellent communication and presentation skills. These positions are eligible for standard Company benefits including medical, dental, vision, time off and 401K, as well as participating in Mineralys incentive plans are contingent on achievement of personal and company performance. Actual compensation may vary from posted hiring range based on geographic location, work experience, education, and/or skill level. US Salary Range:&nbsp; $175,000 - $250,000 #LI-Remote &nbsp; &nbsp; &nbsp;

Director/ Sr. Director, HCP Marketing

Mineralys Therapeutics is a publicly traded, clinical-stage biotechnology company focused on developing medicines to target diseases driven by abnormally elevated aldosterone. Our initial product candidate, lorundrostat, is a proprietary, orally administered, highly selective aldosterone synthase inhibitor that we are developing for cardiorenal conditions affected by abnormally elevated aldosterone, including hypertension and chronic kidney disease. Mineralys is a fully remote company. For more information, please visit&nbsp;https://mineralystx.com. Follow Mineralys on&nbsp;LinkedIn. Pharmacovigilance Scientist The Pharmacovigilance Scientist (PVS) is responsible for providing operational and scientific contributions to Drug Safety, Pharmacovigilance, and Risk Management activities related to the company's product portfolio. This role involves directly conducting safety activities, ensuring compliance with regulatory requirements, and supporting the preparation of safety reports and analyses. Key Responsibilities: Support the PV team in quality control review of individual case safety reports (ICSRs) to ensure accuracy, completeness, and regulatory compliance. Support the Identification and communication of discrepancies or trends in case processing and collaborate on corrective actions. Support and contribute to departmental SOPs and work instructions. Work closely with the Quality Assurance for the finalization of SOPs. Support signal Detection and Management: Conduct regular signal detection activities using various data sources, including spontaneous reports, clinical trial data, and literature. Analyze data to identify potential safety signals and trends. Evaluate the clinical significance of identified signals and recommend appropriate actions. Prepare and present signal detection reports to safety committees and regulatory authorities. Maintain and update signal management plans and documentation. Coordinate and participate in Safety Management Team meetings and clinical study-level Safety Review Committee meetings. Contribute to the preparation of safety documentation for NDA submissions, including Integrated Summary of Safety (ISS), Summary of Clinical Safety and Risk Management Plan (RMP) Assist and contribute to safety sections of the Investigators Brochure and DSUR Assist in preparing and reviewing safety sections of clinical documents and responses to regulatory agency questions. Support audits and inspections related to pharmacovigilance activities. Maintain up-to-date knowledge of global pharmacovigilance regulations and guidelines (e.g., ICH, FDA, EMA). Qualifications Bachelor’s Degree in biologic or natural science, or health case discipline; or Advanced degree preferable (DDS, DMD, BDS, PhD, MPH, NP, PharmD, etc.) required. Minimum of 3 years of Pharmacovigilance experience, including experience in aggregate safety reports and safety signal management. Strong knowledge of global PV regulations and safety databases (Argus). Excellent analytical, communication, and organizational skills. Proficiency in Microsoft Office Suite and safety data management tools. Required Skills Expertise in safety data analysis and signal management. Ability to understand, interpret, analyze, and clearly present scientific and medical data in verbal and written format Prior experience with regulatory submissions and audits. Strong organizational skills, including the ability to prioritize independently with minimal supervision. Strong Pharmacovigilance and drug development foundation, including knowledge of applicable clinical trial safety regulations and post-marketing safety regulations. Includes knowledge of case processing, expedited reporting rules, and safety database concepts. Strong knowledge of common data processing software and database systems such as Argus Strong understanding of US and EU pharmacovigilance regulatory requirements. &nbsp; &nbsp; &nbsp;

Pharmacovigilance Scientist (PV)

Mineralys Therapeutics is a publicly traded, clinical-stage biotechnology company focused on developing medicines to target diseases driven by abnormally elevated aldosterone. Our initial product candidate, lorundrostat, is a proprietary, orally administered, highly selective aldosterone synthase inhibitor that we are developing for cardiorenal conditions affected by abnormally elevated aldosterone, including hypertension and chronic kidney disease. Mineralys is a fully remote company. For more information, please visit&nbsp;https://mineralystx.com. Follow Mineralys on&nbsp;LinkedIn. Senior Director Commercial GMP Quality The Senior Director, Commercial GMP Quality is responsible for leading the development, execution, and continuous improvement of GMP Quality strategies, programs, and systems to support late-stage and commercial manufacturing operations. This role ensures that all products manufactured for Mineralys meet the highest standards of quality and comply with all applicable regulatory requirements, industry best practices, and internal policies. Reporting to the SVP of Quality, this individual serves as a key member of the Quality leadership team and collaborates cross-functionally to drive quality excellence across the product lifecycle. Principal Responsibilities Strategic Leadership &amp; Oversight Lead the development and execution of the Commercial GMP Quality strategy aligned with corporate objectives and regulatory expectations. Serve as the primary GMP Quality leader for commercial manufacturing activities, providing direction and oversight for both internal teams and external partners. Partner with cross-functional leadership to support product launches, tech transfers, and lifecycle management initiatives. Quality Systems &amp; Compliance Oversee the design, implementation, and governance of robust GMP Quality Systems, including but not limited to deviations, CAPAs, change control, batch record review, product disposition, and quality metrics. Ensure continued inspection readiness across all GMP operations, including proactive risk management and mitigation strategies. Batch Release &amp; Product Disposition Provide final Quality review and disposition of commercial drug product and drug substance, ensuring timely release in accordance with regulatory and internal requirements. Ensure compliant and efficient review of master and executed batch records, including investigation resolution and traceability documentation. External Manufacturing Oversight Serve as the senior quality representative for GMP contract manufacturers (CMOs), testing labs, and other service providers supporting commercial operations. Oversee quality agreements, external audits, and performance monitoring to ensure adherence to Mineralys standards and applicable regulations. Regulatory Inspection &amp; Audit Readiness Lead GMP-related inspections and audits (e.g., FDA, EMA) and manage responses and follow-up actions. Direct internal and external audit programs, including risk-based audit planning, execution, and CAPA closure. Quality Culture &amp; Continuous Improvement Foster a proactive quality culture with a focus on continuous improvement, right-first-time execution, and operational excellence. Leverage data and quality metrics to drive decision-making and promote transparency with senior leadership. Skills and Attributes Flexibility to adapt to a fast-changing, ambiguous environment in an organization without fully established procedures Velocity – Drive Speed with Purpose Foresight &amp; Acceleration Execution Under Tight Timelines Clear Decision-Making in Ambiguity Data-Driven Decision Making – Ground Strategy in Evidence Subject Matter Intelligence &amp; Precedent-Based Reasoning Data Interpretation Metrics-Oriented Agile Mindset – Embrace Iteration and Change Adaptability to Shifting Development Plans Iterative Planning &amp; Engagement Frictionless Execution – Simplify the Path to Results Operational Clarity &amp; Precision Lean, Cross-Functional Collaboration Strategic Communication Autonomy – Lead with Ownership and Accountability Self-Directed and Proactive Trusted Decision Maker Leads from the Front Execution that Delivers Value Define success up front Follow through with discipline Deliver results that move the business Travel This position requires up to 25 % travel. &nbsp;Frequently travel is outside the local area and overnight. Some of the travel may be international. &nbsp;Education and Experience Bachelor’s degree in life sciences, chemistry, or related discipline required; Ph.D. or advanced degree preferred Minimum 15 years of experience in GMP Quality Assurance roles within the pharmaceutical or biotech industry, including at least 5 years in a senior leadership capacity Extensive experience in commercial manufacturing, product release, regulatory inspections, and third-party quality oversight Strong knowledge of global GMP regulations and industry best practices These positions are eligible for standard Company benefits including medical, dental, vision, time off and 401K, as well as participating in Mineralys incentive plans are contingent on achievement of personal and company performance. Actual compensation may vary from posted hiring range based on geographic location, work experience, education, and/or skill level. US Salary Range:&nbsp; $To Be Posted #LI-Remote &nbsp; &nbsp; &nbsp;

Senior Director Commercial GMP Quality

Mineralys Therapeutics is a publicly traded, clinical-stage biotechnology company focused on developing medicines to target diseases driven by abnormally elevated aldosterone. Our initial product candidate, lorundrostat, is a proprietary, orally administered, highly selective aldosterone synthase inhibitor that we are developing for cardiorenal conditions affected by abnormally elevated aldosterone, including hypertension and chronic kidney disease. Mineralys is a fully remote company. For more information, please visit&nbsp;https://mineralystx.com. Follow Mineralys on&nbsp;LinkedIn. &nbsp;Our Medical Affairs team is growing and hiring Senior Medical Science Liaison's and Medical Science Liaison's across the US!&nbsp; These field-based medical experts will support the US Medical Affairs team and will focus on establishing, developing, and maintaining strong collaborative relationships through scientific engagement with Key Opinion Leaders and Healthcare Practitioners within the assigned territory. &nbsp;This field position requires a strong background in the pharmaceutical industry, understanding the complexities of healthcare systems, and requires experience in an MSL or MSL like role in cardiovascular disease. Build and maintain relationships with key opinion leaders (KOLs) and healthcare professionals within assigned region Primary point of contact for field medical and scientific inquiries Serve as subject matter expert at key medical and scientific conferences, advisory boards, roundtables, clinical investigator meetings, speaker training, and internal meetings Lead and/or participate in project teams that support MSL strategies and tactics as delegated by MSL leadership Identify and engage with healthcare stakeholders to educate and communicate clinical and scientific data, outcomes, and economic data to providers Deliver scientific presentations and training to diverse HCP audiences with the ability to summarize and communicate complex scientific information in an effective manner Serve as a strategic partner with internal cross-functional teams Support clinical trial site activities as needed and identify/ advocate for opportunities in investigator sponsored trial research Support continuing medical education (CME) requests and activities through unsolicited grants process Support field medical congress activities, and attend national, regional, and local meetings and medical congresses where appropriate to gather competitive intelligence, develop productive medical collaborations, and attend and report on educational sessions Gather, analyze, and communicate actionable insights from the field to inform company strategy, clinical challenges, and patient management trends Participate and contribute in cross-functional meetings, ensuring insights from the field are shared and discussed with Medical Affairs, R&amp;D, Commercial, and other key internal stakeholders Ensure policies, procedures, and guidance are adhered to and Perform all Company business in accordance with all regulations (e.g. EEO FDA, OSHA, PDMA, EPA PhRMA, etc.) Contribute to medical affairs metrics, qualitative and quantitative MSL reports and SOPs for the MSL function. Document all field activities in accordance with company policies and regulatory requirements, ensuring compliance with industry standards Requirements: Pharm.D., Ph.D., M.D. or D.O. (other doctoral degrees considered) &nbsp;For a Senior MSL level we require 5+ years of current MSL experience, and 3 to 5 years of current MSL experience for a Medical Science Liaison in Scientific/Medical Affairs at a biotech or pharmaceutical company Cardiology/Renal/Metabolic experience preferred. 5+ years focused on clinical practice, clinical research, or medical research a plus Experience in a medically related field can include post-doctoral training (i.e., residences and/or fellowships) Experience with all phases of KOL development and HCP engagement with experience with drug launches Skilled in driving cross-functional collaboration, delivering high-quality scientific insights, and consistently achieving measurable outcomes aligned with corporate goals. Strong interpersonal skills including excellent verbal and written communication and peer-to-peer professional collaborations Must be located within driving distance of a major international airport; approx. 50 - 70% travel. Valid US driver’s license required, ability to travel without restrictions. These positions are eligible for standard Company benefits including medical, dental, vision, time off and 401K, as well as participating in Mineralys incentive plans are contingent on achievement of personal and company performance. Actual compensation may vary from posted hiring range based on geographic location, work experience, education, and/or skill level. US Salary Range:&nbsp; $190,000 - $225,000 &nbsp; #LI-Remote &nbsp; &nbsp; &nbsp;

Senior Medical Science Liaisons/ Medical Science Liaisons (MSL) - Cardiovascular

Mineralys Therapeutics is a publicly traded, clinical-stage biotechnology company focused on developing medicines to target diseases driven by abnormally elevated aldosterone. Our initial product candidate, lorundrostat, is a proprietary, orally administered, highly selective aldosterone synthase inhibitor that we are developing for cardiorenal conditions affected by abnormally elevated aldosterone, including hypertension and chronic kidney disease. Mineralys is a fully remote company. For more information, please visit&nbsp;https://mineralystx.com. Follow Mineralys on&nbsp;LinkedIn. The Senior Vice President, Regulatory Affairs reports to the Chief Medical Officer and is responsible for leading Mineralys’ global regulatory function. This individual will play a critical role in shaping and driving successful regulatory outcomes, with particular focus on New Drug Application (NDA) submissions, interactions with regulatory authorities, development-stage and post-approval strategy. Prior experience working at the U.S. Food and Drug Administration (FDA) is strongly preferred and will provide valuable insight into agency expectations and communications. Principal Responsibilities Develop and own the global regulatory strategy through NDA submission and approval. Lead the preparation, submission, and lifecycle management of major regulatory filings. Serve as the primary regulatory voice in cross-functional teams, aligning clinical, CMC, commercial and nonclinical strategies with regulatory expectations. Serve as primary regulatory contact for FDA and other health authorities; lead the planning and execution of regulatory interactions (e.g., Type B and Type C meetings, pre-NDA meetings). Provide expert regulatory input into protocols, study reports, and other key submission documents. Support strategic risk assessments and scenario planning related to regulatory pathways and clinical development. Build and maintain productive relationships with regulatory agencies and external advisors. Provide strategic and operational input, guidance, and oversight to project teams to assure that regulatory submissions and all aspects of regulatory compliance support corporate objectives. &nbsp;Skills and Attributes Velocity – Drive Speed with Purpose Regulatory Foresight &amp; Accelerationwith urgency Execution Under Tight TimelinesManage complex regulatory submissions on compressed schedules without compromising quality.Mobilize teams quickly around high-priority milestones and deadlines. Clear Decision-Making in AmbiguityMove forward with confidence, offering informed paths that balance risk and speed. Data-Driven Decision Making – Ground Strategy in Evidence Regulatory Intelligence &amp; Precedent-Based ReasoningLeverage regulatory precedents, precedent filings, and agency decisions to craft compelling, data-backed strategies. Clinical &amp; CMC Data InterpretationPartner closely with cross functional teams to frame data in a way that is scientifically rigorous Metrics-OrientedDefine and track regulatory success indicators (e.g., meeting outcomes, submission timelines, response quality). &nbsp;Agile Mindset – Embrace Iteration and Change Adaptability to Shifting Development PlansQuickly pivot strategy in response to new clinical data, CMC changes, or regulatory feedback. Iterative Planning &amp; EngagementDesign flexible submission plans and health authority engagement strategies that evolve with program needs. Frictionless Execution – Simplify the Path to Results Operational Clarity &amp; PrecisionStreamline regulatory workflows and documentation processes to minimize rework and improve speed of delivery. Lean, Cross-Functional CollaborationCoordinate seamlessly with other functions to reduce bottlenecks, clarify responsibilities, and keep execution smooth. Strategic CommunicationCommunicate clearly, with minimal noise, from executive summaries to health authority meeting packages. Autonomy – Lead with Ownership and Accountability Self-Directed and ProactiveIdentify risks and opportunities independently and bring forward solutions without waiting for instruction. Trusted Decision MakerServe as the regulatory authority internally by confidently guiding teams and executives on critical go/no-go and submission decisions. Leads from the FrontModel high standards, integrity, quality and accountability acting as a trusted external company representative with regulators and internally at the leadership table. &nbsp;Education and Experience Advanced degree preferred: PharmD, PhD, MD, or equivalent in a scientific or healthcare discipline. 12+ years of progressively responsible experience in Regulatory Affairs within the biopharmaceutical industry, including significant experience leading regulatory strategy. Proven track record of successful NDA submissions and interactions with the FDA and other health authorities. Preferred: Prior experience working at the FDA (e.g., CDER, CBER), offering direct insight into agency expectations and internal processes. Experience spanning the full product lifecycle—from early development through approval and post-marketing regulatory activities. Strong cross-functional leadership experience, particularly with Clinical Development, CMC, Quality, and Commercial teams. Demonstrated ability to manage complex projects, develop regulatory strategies, and lead regulatory interactions globally. Experience in commercial-stage biotech or pharmaceutical environments, with knowledge of regulatory requirements for product labeling, promotional review, and post-marketing commitments. These positions are eligible for standard Company benefits including medical, dental, vision, time off and 401K, as well as participating in Mineralys incentive plans are contingent on achievement of personal and company performance. Actual compensation may vary from posted hiring range based on geographic location, work experience, education, and/or skill level. US Salary Range: $320,000 - $375,000 #LI-Remote &nbsp; &nbsp; &nbsp;

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