- Amgen (Thousand Oaks, CA)
- …and/or oligonucleotide development and commercial lifecycle maintenance, product stability programs, CMC regulatory filings, risk assessment, and Amgen Quality ... us and transform the lives of patients while transforming your career. **Product Quality Director - Synthetics** **What you will do** Let's do this. Let's change the… more
- Gilead Sciences, Inc. (Foster City, CA)
- …PDM functions including Product and Portfolio Strategy, Global Manufacturing,Supply Chain, Regulatory CMC , and the wider Quality organization to achieve ... Join Gilead and help create possible, together. **Job Description** **Senior Director ,** **External Q** **uality Testing** **Operations** This role can be based… more
- Gilead Sciences, Inc. (Foster City, CA)
- …worldwide, with headquarters in Foster City, California. **Senior Director ,** **Product Management** **Team** **Lead** **(Early Phase)** **_Location: Foster ... City_** **KEY RESPONSIBILITIES** Reporting to the Executive Director of Product & Project Management and operating within the broader Pharmaceutical Development and… more
- Gilead Sciences, Inc. (Foster City, CA)
- …countries worldwide, with headquarters in Foster City, California. **Executive Director , Global Clinical Supply Chain (GCSC)** **KEY RESPONSIBILITIES:** Executive ... Director , Global Clinical Supply Chain is responsible for leading...clinical labeling, distribution including cold chain, import/export, reverse logistics, CMC and GXP regulations. + Prior experience in complex… more
- Takeda Pharmaceuticals (Thousand Oaks, CA)
- …effectively with local Technical Services, site leadership, Pharmaceutical Sciences, Global Quality, Regulatory CMC , and other key functions to align on ... the best of my knowledge. **Job Description** **About the role** As Associate Director , Drug Product Manufacturing Science & Technology, you will be Takeda's global… more
- Genentech (South San Francisco, CA)
- …with the people we love. That's what makes us Roche. **The Opportunity** The Director of Cell Engineering in Cell Therapy within gRED (Genentech Research and Early ... development. + Collaborate within Cell Therapy and across the Company (Research, CMC , Genentech, and Roche Subsidiaries) to ensure collective leadership and seamless… more
- University of Southern California (Los Angeles, CA)
- …gene therapies and other biological products for internal/external users. The Associate Director of Process Development (cGMP) is responsible for all aspects of ... interactions and activity prioritization. Regularly ensures compliance with all relevant regulatory requirements. + Oversees the implementation of project plans (eg,… more
- AbbVie (Irvine, CA)
- …required by program needs, in partnership with Discovery, Translational, and CMC colleagues contribute to design and implement translational strategies. May ... strong medical and scientific principles, knowledge of compliance and regulatory requirements, AbbVie's customers, markets, business operations and emerging issues.… more
- Kelly Services (Tarzana, CA)
- …science or engineering discipline. * Understanding of cGMP process and knowledge of CMC regulatory framework for biologics. * Knowledge of aseptic techniques for ... Monica, CA as needed. The contractor will report to the Associate Director of Manufacturing, NGF70. The Specialist, Manufacturing role will ensure successful… more