• cGMP Associate Director , Process…

    University of Southern California (Los Angeles, CA)
    …for product testing. + Lead technology transfer to cGMP manufacturing and quality control , ensuring efficient scaling and implementation. Develop and review ... cGMP Associate Director , Process DevelopmentApply (https://usc.wd5.myworkdayjobs.com/ExternalUSCCareers/job/Los-Angeles-CA Health-Sciences-Campus/cGMP-Associate- Director --Process-Development\_REQ20159691-1/apply) Keck… more
    University of Southern California (06/09/25)
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  • Director , Product Development

    Catalent Pharma Solutions (San Diego, CA)
    …of preclinical and clinical oral and parenteral formulations, and phase appropriate quality control activities. + Understanding of cGMP regulations. The ... **Title: Director Product Development** **About Catalent San Diego:** Catalent,...annually. The Catalent San Diego site is a premier pharmaceutical chemistry development and manufacturing organization supporting the … more
    Catalent Pharma Solutions (06/13/25)
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  • RayzeBio Associate Director

    Bristol Myers Squibb (San Diego, CA)
    …be assigned. + Oversee vendors' activities, and review vendors' deliverables to ensure quality + Create/ QC SDTM/ADaM data specifications, create/ QC CDISC ... in their personal lives. Read more: careers.bms.com/working-with-us . The Associate Director of Biostatistical Programming at RayzeBio will be accountable for… more
    Bristol Myers Squibb (08/30/25)
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  • Director , Global Clinical Compliance (GMP)

    BeOne Medicines (Emeryville, CA)
    …countries/jurisdictions . + Must demonstrate knowledge of the end-to-end manufacturing, labeling, quality control , and release process for clinical supplies and ... **General Description:** The Director Global Clinical Compliance builds, collaborates and manages...drive the compliance activities within Global Clinical Operations. Provides quality guidance, direction and expertise to Clinical Supply GCO… more
    BeOne Medicines (06/07/25)
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  • Associate Director , Regulatory CMC (Small…

    BeOne Medicines (San Mateo, CA)
    …in scientific disciplines and expertise in at least one area in pharmaceutical development (chemical process, formulation, manufacturing, QC , QA, etc.). + ... CMC sections for the assigned project to ensure on-time and high- quality global submissions for investigational, market, and post-approval applications. + Develop… more
    BeOne Medicines (06/25/25)
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  • Associate Director Quality Assurance

    Takeda Pharmaceuticals (Los Angeles, CA)
    …of prevention-based Quality Systems. These systems include exception management, CAPA, Change Control , and Quality on the Shop Floor, all of which are ... **About the role** This position holds ultimate responsibility for the overall Quality Assurance of Site Teardown and Fractionation Operations at Takeda's Los… more
    Takeda Pharmaceuticals (08/23/25)
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  • Director , Submission Operations Management

    BeOne Medicines (Emeryville, CA)
    …as APAC lead and SME for developing global electronic/paper submission processes and quality control procedures. + Align with RIM resources on data remediation, ... supporting functional areas such as CMC, Reg Strategy, Clinical/Non-Clinical, Quality /Manufacturing, GTS, Pharmacovigilance and Regulatory Compliance. This position will… more
    BeOne Medicines (08/01/25)
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  • Principal Biostatistician FSP - Clinical…

    Cytel (Sacramento, CA)
    …with a focus on Neurology therapeutic area. This position reports to the Director of Biostatistics in FSP Services business unit in Cytel. **You will contribute ... PhD strongly desired. + 5+ years supporting clinical trials in the Pharmaceutical or Biotechnology industry. Experience working for a CRO strongly desired. +… more
    Cytel (08/23/25)
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