Cytokinetics is a biopharmaceutical company founded in 1997. Specializing in muscle biology and the potential treatment of serious diseases, Cytokinetics aims to develop innovative therapies that could transform the lives of patients. With a focus on muscle function and the biology of muscle contraction, the company is dedicated to advancing the field of muscle biology research and drug development.

Associate Director, Packaging and Serialization

Senior Director, US Field Excellence & Operations

Associate Director, Clinical Data Management - External Data Solutions

Associate Director, Commercial Learning & Development

Senior Director, Business Insights and Analytics

Director Regulatory Writing (Medical Writer)

Director, Aficamten Global Marketing and Commercial Strategy

Cytokinetics is a late-stage, specialty cardiovascular biopharmaceutical company focused on discovering, developing and commercializing first-in-class muscle activators and next-in-class muscle inhibitors as potential treatments for debilitating diseases in which cardiac muscle performance is compromised. As a leader in muscle biology and the mechanics of muscle performance, the company is developing small molecule drug candidates specifically engineered to impact myocardial muscle function and contractility.At Cytokinetics, each team member plays an integral part in advancing our mission to improve the lives of patients. We are seeking tenacious, compassionate, and collaborative individuals who are driven to make a positive impact. As the Associate Director, External Manufacturing and Supply Operations, you are responsible for operational execution of external manufacturing and related supply activities. This is a central role within Manufacturing and External Supply Operations and requires the ability to manage multiple activities simultaneously, balancing priorities, with a strong sense of urgency, ability to work with ambiguity, and attention to detail. This position will have you collaborating with other members of Supply Chain, Quality Assurance, Regulatory Affairs, and Finance to execute and deliver endorsed global supply plans for both clinical and commercial supply. You will report to the Director, External Supply Operations. Responsibilities Build and maintain productive relationships with external contract manufacturers (CMO’s), and internal global colleagues Ensure timely and effective execution of all manufacturing and supply plans at assigned CMO’s Develop and manage production processes to support operational execution, including BOM’s, specifications, CAPA’s, change controls, master data, and artwork. Familiarity with ERP/MRP systems Support logistics, transportation and import/export activities Act as the manufacturing and supply chain representative for review and approval of documentation including but not limited to batch records, BOM’s, specifications, artwork, and change control Support product qualification activities including but not limited to reviewing/approving IQ/OQ/PQs, stability, and validation protocols; review and approve change controls Play a key role in supporting selection and onboarding of new CMOs, technical transfers, operationalizing product supply and site establishment Manage and track inventory, perform inventory reconciliations, and support month end close process. Issue purchase orders, and track invoices and budgets Maintain production schedules and track batch record execution in coordination with Quality Oversee, review, and approve as necessary revisions to manufacturing cGMP and non GMP documentation Proven risk management acumen with a continuous improvement mindset Where necessary, provide input to the manufacturer and QA for evaluation of process deviations and assist in the investigation of product complaints Build and maintain strong partnerships and provide effective communication with all internal and external stakeholders and lead discussion, problem solving efforts and process improvements to ensure that performance targets are met or exceeded Responsible for scheduling and maintaining routine business operations meetings with CMO’s Support Regulatory submissions and CMC as required Qualifications BS/BA Degree in Life Science, Biology, or Engineering discipline from an accredited college or university, or equivalent desired 10+ years combined experience in manufacturing, outsourced operations, technical operations and/or supply chain in regulated healthcare industry, preferably within biotech/pharmaceutical industry cGMP career experience embedded in a pharmaceutical manufacturing plant is essential – with first-hand knowledge of plant operations, with the insight to assess performance, and diagnose issues directly at the source Technical background with knowledge of engineering and pharmaceutical manufacturing processes in small molecule is required, and experience in DS/API production is desirable Excellent problem-solving skills, with the ability to address complex challenges under time pressure Demonstrated expertise in risk management, with a history of successfully implementing risk mitigation strategies The ability to function in a fast-paced, high-growth, entrepreneurial environment Ability to travel domestically and internationally ~25% Position requires a strong working knowledge and understanding of both regional and international regulations by government agencies affecting the pharmaceutical industry (CFR's, EU GMP, ICH) Timely and effective communication across multiple audiences, both verbally and in writing &nbsp; &nbsp;Our employees come from different backgrounds, and we celebrate those differences. We are looking for the best candidates for our open roles, but do not expect applicants to meet every qualification in order to be considered. If you are excited about what you could accomplish at Cytokinetics and believe you can add value to our team, we would love to hear from you. Please review our General Data Protection Regulation (GDPR) policy PRIOR to applying.&nbsp;&nbsp; Our passion is anchored in robust scientific thinking, grounded in integrity and critical thinking. We keep the patient front and center in all we do – all actions and decisions are in service of the patient and their caregivers. We champion integrity, ethics, doing the right thing, and being our best selves. Fraud Warning: How to Identify Impersonated Cytokinetics Job Postings and Offers Recently, there have been fraudulent employment offers being sent to candidates on behalf of Cytokinetics. Please be advised that all legitimate offers from Cytokinetics will come directly from our official email domain (Cytokinetics.com) and will only be made after completing a formal interview process. Here are some ways to check for authenticity: We do not conduct job interviews through non-standard text messaging applications We will never request personal information such as banking details until after an official offer has been accepted and verified We will never request that you purchase equipment or other items when interviewing or hiring If you are unsure about the authenticity of an offer, or if you receive any suspicious communication, please contact us directly at talentacquisition@cytokinetics.com Please visit our website at: www.cytokinetics.com Cytokinetics is an Equal Opportunity Employer &nbsp;

Associate Director, External Manufacturing and Supply Operations

Cytokinetics is a late-stage, specialty cardiovascular biopharmaceutical company focused on discovering, developing and commercializing first-in-class muscle activators and next-in-class muscle inhibitors as potential treatments for debilitating diseases in which cardiac muscle performance is compromised. As a leader in muscle biology and the mechanics of muscle performance, the company is developing small molecule drug candidates specifically engineered to impact myocardial muscle function and contractility.Reporting directly to the VP, General Manager, DACH, with a dotted line to the Head of Market Access Europe, and as a member of the DACH Leadership Team,&nbsp;the Director Market Access DACH will lead, plan and execute market access strategy, projects and initiatives in Germany, Austria and Switzerland, both on the national as well as on the regional, operative level. They will lead, coordinate and support the German Field Market Access team in their regional and local customer engagements, as well as collaboration with the commercial sales force. Ensuring alignment with the International Market Access team, the Market Access Director will be a dynamic and adaptable leader, responsible for implementing strategies and initiatives that enhance commercial success across all business areas in Germany, Austria and Switzerland. ROLE RESPONSIBILITIES Market Access and Reimbursement Strategy Support national reimbursement strategies across the DACH region, in close collaboration with the DACH leadership team, the company´s international market access functions, and the external market access consultants of the respective country. Support the development of value propositions, evidence packages and reimbursement submissions for favorable Health Technology Assessment (HTA) outcomes and pricing / reimbursement decisions with bodies such as IQWIG, Gemeinsamer Bundesausschuss (G-BA), GKV-SV (Spitzenverband der gesetzlichen Krankenkassen), on the AMNOG reimbursement process in Germany, as well as related institutions in Austria (Dachverband) and Switzerland (BAG). Pricing responsibilities will include pricing assumptions and scenarios for business review and development for the Regional &amp; Global Pricing Committee, when needed. Oversee and lead the planning and execution of pre-launch and launch market access activities. Drive successful launch readiness activities, including reimbursement and pricing negotiations with key regional stakeholders of the respective countries. Ensure pipeline products are appropriately included in country level horizon scanning processes. Develop and execute regional reimbursement strategies and innovative contracting approaches. Monitor and analyze national as well as regional healthcare developments, including cost-effectiveness, reimbursement pathways, early benefit assessments or changes in pharmaceutical funding or purchasing mechanisms. Report trends and adapt strategies, accordingly, in order to minimize price reductions or price reference range . Provide proactive insights and training to commercial team, on strategies to reduce prescription hurdles and enhance product uptake. Lead and Develop Teams The Director Market Access DACH will inspirationally lead the Field Market Access function in Germany, ensuring effective execution of regional access strategies across the 17 KV regions. This includes leading, instructing and training a team of Field Market Access Managers who engage with Commercial Key Account Managers, prescribers, regional payers, healthcare providers, and other key stakeholders to facilitate optimal reimbursement and access conditions for Cytokinetic´s products. The operative support of the Key Account Managers in the field via double visits of important prescribers will be particularly important to address any reimbursement concerns that limit the use of Cytokinetic´s products. Lead, coach, and develop a high-performing team of Field Market Access Managers across Germany. Provide ongoing training and development for the Field Market Access team and other customer-facing roles to ensure excellence in execution and stakeholder engagement. Stakeholder Engagement and Communication Establish and maintain trusted relationships with key opinion leaders (KOLs), sick funds, Regional Associations of SHI Physicians (KVen), regional payor bodies and other relevant stakeholders and decision makers across the DACH region. Understand and address stakeholder needs to support the adoption of innovative therapies. Represent the company in relevant industry associations, forums, and regional events of payers and policy makers. Ensure compliant engagement with external stakeholders, offering value-added services and addressing access barriers. Enhance the company’s reputation by positioning it as a trusted partner within the healthcare ecosystem in the DACH region. Cross-functional Collaboration Collaborate closely with national marketing, medical, sales teams, as well as international market access and HEOR functions, to ensure cohesive strategy execution. Support driving a Key Account Management strategy approach to the markets by integrating market access perspectives into cross-functional customer engagement plans. Facilitate communication and alignment between field and office-based teams. Manage local market access budgets and allocate resources effectively to meet strategic priorities. Data-Driven Decision Making Analyze and present data to inform strategic decisions and track performance against KPIs. Identify and communicate market access trends, opportunities, and risks to internal stakeholders. Communication and Enablement Create and deliver needs-oriented information materials that highlight the value of products and support effective communication with prescribers. Utilize both analog and digital channels to engage with networks and stakeholders effectively. QUALIFICATIONS AND EXPERIENCE Educational Background Bachelor's degree required; advanced university degree preferred, ideally in natural science, business administration, or healthcare-related field. Industry Experience 10+ years of experience in the pharmaceutical or biopharmaceutical industry within market access-related functions. Minimum of 3 years in regional market access or related roles, with demonstrated success in execution of market access strategies in the field on customer level. Healthcare System Expertise Deep understanding of the German, and basic understanding of the Austrian and Swiss healthcare systems, including legal frameworks for pricing and reimbursement. Strong network and stakeholder engagement experience with sick funds and other payor bodies in Germany. Operative experience in Austria and Switzerland is not a must, but beneficial. Stakeholder Management and Communication Proven experience in stakeholder management, with the ability to build resilient networks and influence decision-making. Strong communication and presentation skills, capable of translating complex topics into audience-appropriate formats. High motivation, goal orientation, and a team-oriented, independent working style. Cross-functional and Digital Competence Experience in matrixed, fast-paced organizations and managing cross-functional projects. IT-savvy, with proficiency in modern digital communication channels and MS Office applications. Language and Travel Native-level fluency in German and business-fluent English, both written and verbal. Willingness to travel regularly across the DACH region. What We Offer The privilege to participate in building and shaping the in-country operations of a young, dynamic company in the DACH region, assuming personal responsibility for business-critical projects and processes within a team of highly experienced professionals. An opportunity to join a scientifically outstanding, research-based specialty care pharmaceutical company, shaping the future of innovative treatments in muscle biology. A highly collaborative and inclusive environment which supports professional growth and personal development. A very competitive salary and benefits package above industry average. &nbsp; &nbsp;Our employees come from different backgrounds, and we celebrate those differences. We are looking for the best candidates for our open roles, but do not expect applicants to meet every qualification in order to be considered. If you are excited about what you could accomplish at Cytokinetics and believe you can add value to our team, we would love to hear from you. Please review our General Data Protection Regulation (GDPR) policy PRIOR to applying.&nbsp;&nbsp; Our passion is anchored in robust scientific thinking, grounded in integrity and critical thinking. We keep the patient front and center in all we do – all actions and decisions are in service of the patient and their caregivers. We champion integrity, ethics, doing the right thing, and being our best selves. Fraud Warning: How to Identify Impersonated Cytokinetics Job Postings and Offers Recently, there have been fraudulent employment offers being sent to candidates on behalf of Cytokinetics. Please be advised that all legitimate offers from Cytokinetics will come directly from our official email domain (Cytokinetics.com) and will only be made after completing a formal interview process. Here are some ways to check for authenticity: We do not conduct job interviews through non-standard text messaging applications We will never request personal information such as banking details until after an official offer has been accepted and verified We will never request that you purchase equipment or other items when interviewing or hiring If you are unsure about the authenticity of an offer, or if you receive any suspicious communication, please contact us directly at talentacquisition@cytokinetics.com Please visit our website at: www.cytokinetics.com Cytokinetics is an Equal Opportunity Employer &nbsp;

Director, Market Access DACH

Cytokinetics is a late-stage, specialty cardiovascular biopharmaceutical company focused on discovering, developing and commercializing first-in-class muscle activators and next-in-class muscle inhibitors as potential treatments for debilitating diseases in which cardiac muscle performance is compromised. As a leader in muscle biology and the mechanics of muscle performance, the company is developing small molecule drug candidates specifically engineered to impact myocardial muscle function and contractility.Reporting to the Executive Director, Regulatory Affairs - CMC, the Director of Regulatory Affairs-CMC is responsible for leading regulatory support for assigned programs to ensure sound regulatory planning and tactical implementation of US and international regulatory submission strategies. Responsibilities Formulate CMC regulatory strategies, without supervisor oversight, based on current regulatory intelligence. Collaborates with cross-functional project teams and external business partners to develop CMC regulatory strategies and identify regulatory risks; represents the department in cross-functional project teams. Identifies the required documentation and any content, quality and timeline issues for global submissions and manages the delivery of approved technical documents in accordance with project timelines. Manages the preparation, authoring and maintenance of regulatory submission documents pertaining to CMC data for global clinical trial and marketing applications, as well as post-marketing variations. May require technical regulatory authoring of submission package components. Supports the evaluation of manufacturing changes for the potential impact on products. Provides expert review of CMC documentation supporting regulatory submissions and communications. Coordinates preparation of responses to queries from regulatory authorities, particularly focused on CMC. May require technical regulatory authoring to support responses to queries. Maintains knowledge and expertise with FDA/EMA regulations, ICH guidelines and other international regulatory regulations and guidelines, as needed to support global programs. Ensures conformance to commitments made with various regulatory agencies (e.g., IND/CTA commitments) for assigned programs. Provides regulatory advice to other functional areas. May participate in regulatory due diligence activities. Relationships Build and maintain collaborative relationships with internal/external business partners to achieve project regulatory goals. Develops and maintains collaborative relationships with other departments to ensure effective communication regarding project regulatory goals, issues and timelines. Develop and manage relationships with external vendors and regulatory health authorities. Coordinates activities for meetings and conferences with FDA, EMA, and other regulatory authorities Collaborate with regulatory colleagues to provide CMC expertise as needed. Management This is an Individual Contributor position; however, there is the possibility for supervising consultants/contractors and/or interns. Develops and implements regulatory operating guidelines and common work practices/strategies within the team. Qualifications 10 - 12+ years of related work experience (Director candidates will typically bring 12+ years; Associate level candidates may be considered with 10+ years and strong potential), including 8+ years in Regulatory Affairs CMC in the Biotech/Pharmaceutical industry; experience in small molecule drug development required; experience in the cardiovascular therapeutic area is a plus Proven experience serving as a primary RA-CMC contact to Health Authorities, with full strategic responsibility. Bachelor’s degree is required, preferably in chemistry or a closely related field; advanced degree is a plus. Advanced degree is preferred. Excellent working knowledge of international regulatory requirements and environment, including an understanding of GXP Solid working knowledge of core processes associated with discovery, development, and manufacturing of small molecules. Experience with eCTD requirements and electronic submissions Experience with international regulatory submissions and processes is a strong plus. Ability to work effectively across teams, functions and with outside partners. Excellent oral and written communication skills Excellent organizational skills and attention to detail Our employees come from different backgrounds, and we celebrate those differences. We are looking for the best candidates for our open roles, but do not expect applicants to meet every qualification in order to be considered. If you are excited about what you could accomplish at Cytokinetics and believe you can add value to our team, we would love to hear from you. Please review our General Data Protection Regulation (GDPR) policy PRIOR to applying.&nbsp;&nbsp; Our passion is anchored in robust scientific thinking, grounded in integrity and critical thinking. We keep the patient front and center in all we do – all actions and decisions are in service of the patient and their caregivers. We champion integrity, ethics, doing the right thing, and being our best selves. Fraud Warning: How to Identify Impersonated Cytokinetics Job Postings and Offers Recently, there have been fraudulent employment offers being sent to candidates on behalf of Cytokinetics. Please be advised that all legitimate offers from Cytokinetics will come directly from our official email domain (Cytokinetics.com) and will only be made after completing a formal interview process. Here are some ways to check for authenticity: We do not conduct job interviews through non-standard text messaging applications We will never request personal information such as banking details until after an official offer has been accepted and verified We will never request that you purchase equipment or other items when interviewing or hiring If you are unsure about the authenticity of an offer, or if you receive any suspicious communication, please contact us directly at talentacquisition@cytokinetics.com Please visit our website at: www.cytokinetics.com Cytokinetics is an Equal Opportunity Employer &nbsp;

Director, Regulatory Affairs CMC

Cytokinetics is a late-stage, specialty cardiovascular biopharmaceutical company focused on discovering, developing and commercializing first-in-class muscle activators and next-in-class muscle inhibitors as potential treatments for debilitating diseases in which cardiac muscle performance is compromised. As a leader in muscle biology and the mechanics of muscle performance, the company is developing small molecule drug candidates specifically engineered to impact myocardial muscle function and contractility.At Cytokinetics, each team member plays an integral part in advancing our mission to improve the lives of patients. We are seeking tenacious, compassionate, and collaborative individuals who are driven to make a positive impact. The Regional Sales Manager&nbsp;leads a high-performing team to drive growth across the region, with a strong focus on strategic execution, customer engagement, and cross-functional collaboration. This role is responsible for developing and executing business plans, cultivating relationships with key healthcare professionals, ensuring regulatory compliance, and fostering a results-oriented, patient-centric culture. This is a senior-level commercial leadership position within the pharmaceutical (biotech) industry, ideally suited for someone who thrives on high-level scientific exchange and finds purpose in bringing first-in-class treatments to patients—positively impacting their lives and those of their families. The Regional Sales Manager will lead a team of dedicated Key Account Managers within the assigned region. The role offers a high degree of autonomy and visibility, along with a unique opportunity to shape how Cytokinetics is positioned in the DACH region. ROLE RESPONSIBILITIES Leadership &amp; Team Development Recruit, lead, coach, and mentor a high-performing team of Key Account Managers. Conduct regular field visits and coaching sessions to ensure effective sales execution. Set and monitor individual and team goals, including incentive plans and development objectives. Foster a collaborative, patient-centric, and results-driven culture. Ensure appropriate training, learning, and personal development opportunities for all team members. Establish and maintain a positive and motivating working environment. Role model Cytokinetics´ company values. Sales &amp; Market Strategy Execution Develop and execute a strategic regional business plan aligned with national objectives, in close collaboration with the DACH Leadership Team. Define and implement segmentation and targeting strategies for key local prescriber groups. Co-establish sales objectives with country leadership by forecasting and setting annual quotas, projecting sales volumes and market shares for existing and new products. Monitor regional performance against targets, analyze gaps, and adjust strategies proactively. Implement and oversee the rollout of CRM systems and tools to support sales effectiveness. Market &amp; Customer Engagement Build and maintain strong relationships with Key Opinion Leaders (KOLs), healthcare professionals (HCPs), and key accounts. Educate providers on the clinical benefits and appropriate use of the company’s therapies. Collaborate cross-functionally with medical, market access, and marketing teams to ensure aligned customer engagement and product support. Develop and implement account action plans to drive in-label usage of approved products within the appropriate patient populations. Compliance &amp; Operational Excellence Ensure full adherence to regulatory, legal, and compliance standards. Promote ethical sales practices and maintain accurate documentation. Monitor competitive trends and market dynamics, adjusting strategies as needed. Complete operational requirements by scheduling and assigning responsibilities and following up on execution and results. QUALIFICATIONS AND EXPERIENCE Educational Background Bachelor’s degree required; advanced degree in Life Sciences or an MBA is preferred. Industry Experience Minimum of 10 years of experience in the pharmaceutical or biotechnology industry in field-based sales roles. At least 2 years of proven success in sales leadership, ideally in regional management within smaller, agile team environments. Demonstrated experience in product launches and driving regional sales growth. Experience in specialized cardiology indications would be beneficial, but not a requirement. Skills &amp; Attributes Strong leadership, coaching, and team-building capabilities. Strategic thinker with solid business acumen and the ability to develop and execute regional sales strategies. Excellent communication, negotiation, and analytical skills. Creative, curious, and solutions-oriented with a hands-on, can-do attitude. Comfortable advocating for the value and pricing of innovative pharmaceutical products. Proficiency in Microsoft Office Suite and CRM tools. Language &amp; Communication Business fluency in German and a high level of proficiency in English are required. Travel &amp; Location Willingness and ability to travel extensively (up to 65%) across large territories; this is a 100% field-based role. What We Offer The privilege to participate in building and shaping the in-country operations of an exciting, dynamic company in the DACH region, assuming personal responsibility for business-critical projects and processes within a team of highly experienced professionals. An opportunity to join a scientifically outstanding, research-based specialty care pharmaceutical company, shaping the future of innovative treatments in muscle biology. A highly collaborative and inclusive environment which supports professional growth and personal development. A very competitive salary and benefits package above industry average. &nbsp; &nbsp; &nbsp;Our employees come from different backgrounds, and we celebrate those differences. We are looking for the best candidates for our open roles, but do not expect applicants to meet every qualification in order to be considered. If you are excited about what you could accomplish at Cytokinetics and believe you can add value to our team, we would love to hear from you. Please review our General Data Protection Regulation (GDPR) policy PRIOR to applying.&nbsp;&nbsp; Our passion is anchored in robust scientific thinking, grounded in integrity and critical thinking. We keep the patient front and center in all we do – all actions and decisions are in service of the patient and their caregivers. We champion integrity, ethics, doing the right thing, and being our best selves. Fraud Warning: How to Identify Impersonated Cytokinetics Job Postings and Offers Recently, there have been fraudulent employment offers being sent to candidates on behalf of Cytokinetics. Please be advised that all legitimate offers from Cytokinetics will come directly from our official email domain (Cytokinetics.com) and will only be made after completing a formal interview process. Here are some ways to check for authenticity: We do not conduct job interviews through non-standard text messaging applications We will never request personal information such as banking details until after an official offer has been accepted and verified We will never request that you purchase equipment or other items when interviewing or hiring If you are unsure about the authenticity of an offer, or if you receive any suspicious communication, please contact us directly at talentacquisition@cytokinetics.com Please visit our website at: www.cytokinetics.com Cytokinetics is an Equal Opportunity Employer &nbsp;

Regional Sales Manager

Cytokinetics is a late-stage, specialty cardiovascular biopharmaceutical company focused on discovering, developing and commercializing first-in-class muscle activators and next-in-class muscle inhibitors as potential treatments for debilitating diseases in which cardiac muscle performance is compromised. As a leader in muscle biology and the mechanics of muscle performance, the company is developing small molecule drug candidates specifically engineered to impact myocardial muscle function and contractility.Cytokinetics is seeking a highly experienced Senior Director, Commercial Regulatory Affairs and Business Operations, to join the Regulatory Affairs team in Europe. They will play a key role in ensuring that all promotional materials and activities comply with regional and local regulatory requirements, aligning with the company's commercial objectives. This role is also pivotal in ensuring the efficient and compliant operation of our regulatory affairs department, with a focus on collaborating with the general managers and regulatory local vendors across our affiliates in Europe. They will help develop the infrastructure of the Regulatory Affairs Department in Europe, including implementation of process improvements to enhance the efficiency of operations as well as oversight of regulatory policy changes in Europe and their impact on business operations.The ideal candidate will possess a strong experience and understanding of regulatory requirements and processes related to promotion and commercialization, excellent organizational skills, and the ability to work effectively with cross-functional teams to streamline operations and support business objectives.Responsibilities Advertising and promotional activities: Lead and manage the European MLR process, ensuring timely and compliant regulatory review of promotional and non-promotional materials in Europe. Training and Guidance: Provide training and guidance to internal teams on regulatory requirements and best practices for promotional activities and other activities as required. Oversight of local regulatory activities: Develop and oversee the local regulatory activities through vendor selection, management and serve as the primary liaison between the central regulatory affairs team and local regulatory vendors, ensuring alignment of regulatory strategies and objectives. Cross-Functional Collaboration: Work closely with internal departments, including Pharmacovigilance, Quality Assurance, Commercial and Medical teams, to ensure regulatory activities are conducted timely and compliantly. Regulatory Compliance: Ensure all regulatory activities are conducted in compliance with applicable regulations and guidelines, maintaining up-to-date knowledge of regulatory requirements in each country’s jurisdiction. Standard Operations Procedures development: work cross functionally to ensure all relevant regulatory SOPs at regional and local levels are in place. Budget management: Help manage and coordinate budget of the regulatory department in Europe and provides input into budgeting and resource requirements. Process Improvement: Identify opportunities for process enhancements within the regulatory affairs function to increase efficiency and compliance. Regulatory Intelligence: Oversee the regulatory policy requirements changes in Europe and ensure timely communication of impacts to relevant stakeholders. Qualifications Seasoned professional with a minimum of 12 years of relevant experience with solid expertise and knowledge of the applicable European regulatory regulations, directives and guidelines Strong experience understanding of European regulatory requirements, particularly concerning promotional activities. Prior experience in advertising and promotion regulatory roles is a must. Must have experience dealing with regulatory representatives in the EU countries. Must have solid understanding of quality and GxP standards. Excellent communication and leadership skills. Ability to work effectively in a cross-functional, matrixed environment. Must be a strong team player, a fully engaged, hands-on professional capable of working collaboratively and independently, with excellent verbal and written communication skills. Excellent planning, organization and time management skills including the ability to support and prioritize multiple projects. Strong interpersonal capabilities and ability to build and maintain networks. Possesses sense of urgency; identifies challenges and problems and takes the initiative to identify solutions. Our employees come from different backgrounds, and we celebrate those differences. We are looking for the best candidates for our open roles, but do not expect applicants to meet every qualification in order to be considered. If you are excited about what you could accomplish at Cytokinetics and believe you can add value to our team, we would love to hear from you. Please review our General Data Protection Regulation (GDPR) policy PRIOR to applying.&nbsp;&nbsp; Our passion is anchored in robust scientific thinking, grounded in integrity and critical thinking. We keep the patient front and center in all we do – all actions and decisions are in service of the patient and their caregivers. We champion integrity, ethics, doing the right thing, and being our best selves. Fraud Warning: How to Identify Impersonated Cytokinetics Job Postings and Offers Recently, there have been fraudulent employment offers being sent to candidates on behalf of Cytokinetics. Please be advised that all legitimate offers from Cytokinetics will come directly from our official email domain (Cytokinetics.com) and will only be made after completing a formal interview process. Here are some ways to check for authenticity: We do not conduct job interviews through non-standard text messaging applications We will never request personal information such as banking details until after an official offer has been accepted and verified We will never request that you purchase equipment or other items when interviewing or hiring If you are unsure about the authenticity of an offer, or if you receive any suspicious communication, please contact us directly at talentacquisition@cytokinetics.com Please visit our website at: www.cytokinetics.com Cytokinetics is an Equal Opportunity Employer &nbsp;

Senior Director, Commercial Regulatory Affairs and Business Operations - Europe

Cytokinetics is a late-stage, specialty cardiovascular biopharmaceutical company focused on discovering, developing and commercializing first-in-class muscle activators and next-in-class muscle inhibitors as potential treatments for debilitating diseases in which cardiac muscle performance is compromised. As a leader in muscle biology and the mechanics of muscle performance, the company is developing small molecule drug candidates specifically engineered to impact myocardial muscle function and contractility.At Cytokinetics, each team member plays an integral part in advancing our mission to improve the lives of patients. We are seeking tenacious, compassionate, and collaborative individuals who are driven to make a positive impact. The Inventory and Operations Manager is responsible for overseeing the execution of processes that support the manufacturing and movement of pharmaceutical products throughout the value chain. This role ensures accurate inventory management across the supply network and plays a crucial role in facilitating timely transactional activities, including goods receipts, issues, and product movements. As a key Subject Matter Expert (SME) in Planning &amp; Inventory Operations, the manager leads the design and development of processes, creating process maps, process design documentation, and training materials. Additionally, they serve as stewards of master data, actively managing and promoting Master Data Management practices to ensure data integrity across the supply chain. Key Responsibilities Process Execution and Data Stewardship Work with suppliers, manufacturers, and third-party logistics providers to ensure timely and efficient execution of supply chain transactions across the value chain Perform goods receipts, goods issues, transfers, and other goods movements in support of Supply Execution at external suppliers, warehouses and distribution centers Works closely with the Quality team to ensure accurate product status for all inventory at third-party sites and assists in resolving any related issues Conducts regular inventory audits and reconciles discrepancies between physical stock and records Works closely with the Finance team to ensure accurate and correct inventory valuation throughout the value chain Collaborates closely with Procurement and Logistics on status on inbound and outbound material and product inventory Partners with the Planning team on product demand and scenario planning to manage inventory Serves as the steward for Master Data Management supporting the flawless execution of Supply Chain process execution for inventory management Process Subject Matter Expert (SME) Oversee the end-to-end pharmaceutical supply chain process design as a key Subject Matter Expert (SME), across the Value Chain for inventory management Develop Process Maps, Process Documentation, and Training materials supporting execution across Value Chain inventory processes Create and own user training and development documentation supporting end user execution and ensure all users are trained and knowledgeable of all value chain inventory processes Regulatory Compliance &amp; Documentation: Ensure adherence to pharmaceutical industry regulations, including Good Manufacturing Practices (GMP), Good Distribution Practices (GDP), and other relevant compliance standards Maintain accurate and up-to-date records for all inventory transactions, including receipts, shipments, and goods movements Performance Reporting and Analysis: Develop and maintain key performance indicators (KPIs) to assess inventory accuracy and management, and process performance across the value chain Identify and implement process improvements to streamline inventory and supply chain operation to help ensure inventory availability, reduce costs and enhance customer satisfaction Continuous Improvement: Evaluate current processes and identify opportunities for improvement in supply chain and inventory management practices Stay current with industry trends, technologies, and best practices to continually enhance supply chain efficiency and inventory control Qualifications Bachelor’s degree in Supply Chain Management, Industrial Engineering, Business Administration, or a related field Master’s degree or MBA preferred, with additional certifications in supply chain (e.g., APICS, Six Sigma, PMP) Minimum 5+ years of experience in supply chain, inventory management, or supply operations within the pharmaceutical or healthcare industry Experience working with supply chain management software and ERP systems (e.g., Oracle, SAP, or similar) Familiarity with pharmaceutical supply chain regulations and industry best practices Ability to work under pressure, manage competing priorities, and meet deadlines Strong attention to detail and commitment to maintaining high-quality standards Ability to travel as required to support inventory management processes and audits Our employees come from different backgrounds, and we celebrate those differences. We are looking for the best candidates for our open roles, but do not expect applicants to meet every qualification in order to be considered. If you are excited about what you could accomplish at Cytokinetics and believe you can add value to our team, we would love to hear from you. Please review our General Data Protection Regulation (GDPR) policy PRIOR to applying.&nbsp;&nbsp; Our passion is anchored in robust scientific thinking, grounded in integrity and critical thinking. We keep the patient front and center in all we do – all actions and decisions are in service of the patient and their caregivers. We champion integrity, ethics, doing the right thing, and being our best selves. Fraud Warning: How to Identify Impersonated Cytokinetics Job Postings and Offers Recently, there have been fraudulent employment offers being sent to candidates on behalf of Cytokinetics. Please be advised that all legitimate offers from Cytokinetics will come directly from our official email domain (Cytokinetics.com) and will only be made after completing a formal interview process. Here are some ways to check for authenticity: We do not conduct job interviews through non-standard text messaging applications We will never request personal information such as banking details until after an official offer has been accepted and verified We will never request that you purchase equipment or other items when interviewing or hiring If you are unsure about the authenticity of an offer, or if you receive any suspicious communication, please contact us directly at talentacquisition@cytokinetics.com Please visit our website at: www.cytokinetics.com Cytokinetics is an Equal Opportunity Employer &nbsp;

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