- Gilead Sciences, Inc. (Foster City, CA)
- …their aspirations. Join Gilead and help create possible, together. **Job Description** **Senior Director , Biologics Drug Product MSAT** Gilead Sciences, ... across a global production network. We are accountable for direct technical support of drug substance and drug product operations, with responsibility for… more
- Gilead Sciences, Inc. (Foster City, CA)
- …cancer and inflammation, and serious respiratory and cardiovascular conditions. ** Director , CMC Regulatory Affairs - Biologics ** **Key Responsibilities:** ... unmet medical need. With each new discovery and investigational drug candidate, we seek to improve the care of...The Director , CMC Regulatory Affairs for Biologics is responsible for defining regulatory strategy for one… more
- Gilead Sciences, Inc. (Foster City, CA)
- …together. **Job Description** We are currently seeking an industry leader for a Director , Quality Assurance role, who will report to Executive Director , Supplier ... + Support and/or conduct audits of providers of raw materials, product contact consumables, contract manufacturing or testing, software, warehouse / distribution… more
- BeiGene (Emeryville, CA)
- …more major geographic areas, and prior experience with both small molecules and biologics . + Thorough understanding of drug development process and the ... The Executive Director , Global Regulatory Portfolio Lead will be responsible...development programs to secure and maintain market access for product (s) in line with business objectives, and in coordination… more
- BeiGene (Emeryville, CA)
- **General Description** **_:_** + The Director , Global Regulatory Lead, will be responsible for developing, implementing, and advising on global regulatory ... strategies for development programs to secure and maintain market access for product (s) in line with business objectives, and in coordination with key internal… more
- BeiGene (Emeryville, CA)
- **General** **Description:** The Senior Director of CMO and Distribution Logistics, Clinical Supply Chain is responsible for overseeing the Clinical Supply Chain ... establishing QA and MSA agreements with all CMO's and assuring that Product Specific Requirements (PSR's) are established before projects are initiated. +… more