- Gilead Sciences, Inc. (Foster City, CA)
- …will assume a full-time employment role in the capacity of Senior Associate in Gilead's Regulatory Affairs CMC department. **Job Description:** + ... countries worldwide, with headquarters in Foster City, California. **Sr. Associate , CMC Regulatory Affairs -...detail. Work is performed under limited direction of a senior Regulatory Affairs professional. **Minimum Qualifications:** +… more
- Frontier Medicines (South San Francisco, CA)
- Join Frontier Medicines on an exciting journey as our newest Senior Manager/ Associate Director in CMC Development, located at either our Boston or South San ... of our team, reporting directly to the Head of CMC , you'll play an integral role in advancing our...thorough understanding of ICH guidelines, GLP/GMP manufacturing, and related regulatory requirements is required + Ability to travel domestically… more
- Ascendis Pharma (Palo Alto, CA)
- …and those of direct reports. + Work is performed under direction of a Senior Regulatory Affairs professional. + Contribute to internal regulatory policies ... a dynamic workplace for employees to grow and develop their skills. The Associate Director, Regulatory Affairs will be responsible for developing and… more
- BeiGene (Emeryville, CA)
- …Will work cross functionally and collaboratively in BeiGene with eg Manufacturing, Supply Chain, Regulatory CMC and other Quality teams like QPs in EU. + Provide ... **General Description:** The Associate Director, DP Commercial Small Molecule in External...and GxP guidelines + Work with Clinical Product Quality, regulatory and CMC to establish Process Performance… more
- Gilead Sciences, Inc. (Foster City, CA)
- …and help create possible, together. **Job Description** **Key Responsibilities** Associate II, Global External Manufacturing, Small Molecule Drug Substance (DS) ... external contract manufacturing network, while ensuring compliance with cGMP, regulatory requirements, and environmental, health, and safety legislations. This… more