- Gilead Sciences, Inc. (Foster City, CA)
- …to fulfil their aspirations. Join Gilead and help create possible, together. **Job Description** ** Senior Director , Biologics Drug Product MSAT** Gilead ... are benefiting hundreds of thousands of people, a pipeline of late-stage drug candidates, and unmatched patient access programs to ensure medications are available… 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 ... distribution and logistics teams for storage, Import & Export, distribution, drug return, destruction, and Depot Management. + Accountable for ensuring successful… 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 ... to address compliance concerns identified during audits are commensurate with current biologics industry practices and benchmarks + Ensure that the audit agenda is… more
- BeiGene (Emeryville, CA)
- …strategies to mitigate risks and support development of small molecule and/or biologics drug candidates from pre-IND and first-in- human testing through ... **General Description:** The Director , Clinical Pharmacology & Pharmacometrics will be responsible...pharmacology and pharmacometric strategies for novel small molecules and biologics assets in the company portfolio. She/He will provide… 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...and cross-functional influence and acts as an advisor/liaison to senior management and project teams to plan, evaluate and… more
- BeiGene (Emeryville, CA)
- **General Description** **_:_** + The Director , Global Regulatory Lead, will be responsible for developing, implementing, and advising on global regulatory ... with global regulatory authorities as needed for all aspects pertaining to drug development including resolution of key regulatory issues and to expedite approvals… more