Cytokinetics is a late-stage biopharmaceutical company specializing in the discovery, development, and commercialization of muscle activators and inhibitors to treat debilitating diseases affecting muscle performance. As leaders in muscle biology, they develop small molecule drugs targeting muscle function and contractility, with a focus on treating heart failure, Amyotrophic Lateral Sclerosis, and Hypertrophic Cardiomyopathy. Recognized for their innovative approach and workplace culture, Cytokinetics has been honored as a Best Place to Work multiple times.
Open Positions
Contractor – Sr. Quality Associate
5 years of experience in a life sciences Quality environment, Bachelor's degree in a related scientific discipline, strong working knowledge of GxP requirements and regulated documentation practices
Medical Science Liaison (TMS)
Advanced degree in biomedical sciences, 3+ years of Medical Affairs experience, strong business acumen, excellent communication skills, and proficiency in Microsoft Office and web-based applications
Director, Packaging and Artwork Management
10+ years of experience in pharmaceutical packaging and artwork management, leadership and stakeholder management skills, and ability to drive execution in resource-constrained settings
Director of Quality Assurance, Alliance Management
10+ years experience in pharma/biopharma, cGMP regulations, and biopharma/start-up environment
Associate Director, External Manufacturing and Supply
BS/BA degree in Life Science, Biology, or Engineering, 10+ years combined experience in manufacturing, outsourced operations, technical operations, and/or supply chain, cGMP career experience in pharmaceutical manufacturing plant
Senior Medical Director, UK
7 years of pharmaceutical industry experience, MD/MBBS with strong Medical Affairs experience, and medical Affairs experience in the UK
Marketing Director France & Benelux
Marketing experience with leadership skills and a hands-on approach. Ability to operate in complex environments and manage multiple priorities
Director, Regulatory Affairs CMC
10-12+ years exp. Biotech/Pharmaceutical experience, 8+ yrs in Regulatory Affairs CMC; Bachelor's degree req. Advanced degree preferred. Strong understanding of GXP and international regulations
Senior Manager, Supply Chain & Technical Project Management
10-20% Travel, BA/BS in Scientific, Technical, Engineering or Business discipline (advanced degree preferred), 10+ years experience in project management
Manager, External Manufacturing and Supply
BS/BA Degree in Life Sciences, Engineering, or related discipline. 10+ years experience in pharmaceutical manufacturing, technical operations, or external supply in a regulated environment