Cytokinetics Inc jobs

Director, Global Data Strategy & Operations Radnor, Pennsylvania posted: Posted 30+ Days Ago

Associate Director, Drug Product MS&T Ireland posted: Posted 17 Days Ago

Associate Director, External Manufacturing & Supply Operations Ireland posted: Posted 2 Days Ago

Director, Patient Support Services Strategy and Operations 2 Locations posted: Posted Yesterday

Director, Regulatory Affairs CMC Europe Zug, Switzerland 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. 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

Associate Director, Field Deployment & Incentive Compensation 2 Locations posted: Posted 30+ Days Ago

Associate Director, Sourcing & Supplier Relationship Management Dublin, Dublin, Ireland 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. As Associate Director, Sourcing & Supplier Relationship Management, you will play a critical role in ensuring the suppliers and partners we work with meet our high standards for quality, innovation, and patient impact. This role plays a critical part in the comprehensive lifecycle of Cytokinetics relations with partners and suppliers supporting Global Supply Chain & Technical Operations. This role requires strong strategic thinking, broad industry experience and excellent relationship development and management skills. This role will support our Sourcing and Network Strategy pillar, a key component of our Global Supply Chain & Technical Operations strategy. This role will support our Manufacturing and Lab Services Supplier Strategy, marketplace assessments of supplier capabilities from early development thru post approval Commercialization, supplier due diligence through Request for Information (RFI) and Requests for Proposals (RPF). These due diligence activities will lead to collaborative supplier selection, contract negotiations, operationalization of the relationship and ultimately management of supplier performance against the contract. This role will be a key partner to CMC and Technical Operations, External Manufacturing and Supply Operations, Enterprise Risk Management, Supply

Principal Scientist, Computational Chemistry South San Francisco, California posted: Posted 22 Days Ago

Senior Director, CMC Lead Product Development South San Francisco, California posted: Posted 15 Days Ago

Marketing Lead France & Benelux France 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. As part of the Commercial organization, this role plays a key role in driving the marketing strategy and execution for innovative cardiovascular therapies across France & Benelux. Reporting to the Head of Commercial France & Benelux, the position combines strategic contribution with strong operational leadership to support successful product launches and sustainable brand growth. The role works in close partnership with cross-functional teams including Medical Affairs, Regulatory, Market Access, and Sales, as well as with Global and Regional Marketing counterparts. The incumbent contributes to the adaptation and evolution of brand strategy, ensures effective omnichannel execution, and supports business performance while maintaining full compliance with internal and external requirements. Key Responsibilities Lead the development, adaptation, and delivery of local marketing strategies and plans in alignment with global and regional brand frameworks. Contribute to the evolution of brand positioning, value propositions, and lifecycle priorities by integrating local market insights, competitive intelligence, and customer needs. Build and steer comprehensive pre-launch, launch and post-launch plans, ensuring cross-functional alignment, planning and execution readiness. Translate scientific and clinical data into clear, compelling, and differentiated customer narratives. Drive

Medical Affairs Operations Specialist South San Francisco, California posted: Posted 4 Days Ago

Associate Director, Medical Science Liaison (MSL) 3 Locations posted: Posted 30+ Days Ago

Senior Director, Regulatory Affairs REMS Program South San Francisco, California posted: Posted 2 Days Ago

Cardiovascular Account Specialist - U.S. Sales, New Haven, CT Remote posted: Posted 11 Days Ago

Senior Director, FP&A, Global Supply Chain and Technical Operations South San Francisco, California posted: Posted 9 Days Ago

Associate Director, Medical Science Liaison (MSL) - Central & Southern Florida, Puerto Rico 3 Locations posted: Posted 15 Days Ago

Contractor – Sr. Quality Associate Dublin, Dublin, Ireland 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. Job purpose The role will provide structured assistance across document management, complaints handling, reporting, and general administrative activities. Securing this support will improve operational efficiency, strengthen compliance, and enable QA professionals to focus on high-value quality and oversight responsibilities. The Quality Department operates in a highly regulated environment with increasing demands related to documentation, customer assurance, and quality reporting. QA administrative workload has grown significantly, particularly in areas such as complaints management, CMO scorecard development, and compliance checks. Responsibilities The Quality Associate support will initially provide approximately 20 hours per week of support across the following key areas Document Creation and Execution Support Preparation, formatting, and maintenance of QA documentation within Veeva Coordination of document lifecycle activities including review and version control Ensuring adherence to internal documentation standards Complaints Management Support Initiating and tracking of customer complaints Supporting data entry, documentation, and follow-up activities Assisting in maintaining audit-ready complaint records CMO Scorecard Development Supporting data collection and consolidation for CMO performance metrics Assisting in the preparation and formatting of scorecards and reports Maintaining consistency and accuracy in reporting outputs

Associate Director, External Manufacturing & Supply Operations Ireland posted: Posted Today

Senior HCP Marketing Manager Radnor, Pennsylvania posted: Posted 14 Days Ago

Director of Quality Assurance, Alliance Management 2 Locations posted: Posted 22 Days Ago

Associate Director, Clinical Quality Assurance Auditor Remote posted: Posted 30+ Days Ago

Associate Director, QA Computer System Validation Radnor, Pennsylvania posted: Posted 15 Days Ago

Associate Director, External Manufacturing and Supply Dublin, Dublin, Ireland 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. Job purpose 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

Manager, External Manufacturing and Supply Dublin, Dublin, Ireland 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. Job purpose As a Manager, External Manufacturing and Supply Operations, you are responsible for the end-to-end technical and operational oversight of external manufacturing and supply activities across a network of Contract Manufacturing Organizations (CMOs). This role sits at the core of Manufacturing and External Supply Operations and requires a strong technical foundation, the ability to manage multiple concurrent priorities, and to operate effectively in a fast-paced, ambiguous environment. This position places particular emphasis on batch record review and approval, process oversight, and technical decision-making, ensuring that manufacturing activities are executed in full compliance with cGMP standards and aligned with global supply requirements. You will collaborate cross-functionally with Quality Assurance, Technical Operations, Regulatory Affairs, and Supply Chain to ensure robust, compliant, and reliable supply for both clinical and commercial products. You will report to the Director, External Supply Operations. Responsibilities Build and maintain strong, technically credible relationships with external CMOs and internal cross-functional stakeholders Provide hands-on technical oversight of manufacturing operations at CMOs, ensuring adherence to validated processes, regulatory expectations, and internal standards Own and lead the review and approval