• cGMP Associate Director

    University of Southern California (Los Angeles, CA)
    cGMP Associate Director , Process DevelopmentApply (https://usc.wd5.myworkdayjobs.com/ExternalUSCCareers/job/Los-Angeles-CA Health-Sciences-Campus/ cGMP ... and other biological products for internal/external users. The Associate Director of Process Development ( cGMP ) is responsible for all aspects of… more
    University of Southern California (09/08/25)
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  • Associate Director , Process

    Gilead Sciences, Inc. (Foster City, CA)
    …their aspirations. Join Gilead and help create possible, together. **Job Description** ** Associate Director , Process Technologies and Development** Gilead ... with life-threatening diseases. Qualified candidates will be part of the process technologies and development group, acting as an interface between formulation… more
    Gilead Sciences, Inc. (09/05/25)
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  • Associate Director , MSAT,…

    Otsuka America Pharmaceutical Inc. (Sacramento, CA)
    **Job Summary** **​** The Associate Director , MSAT - Downstream provides specialized technical leadership and oversight for all downstream manufacturing ... of downstream operations through effective technology transfer, validation support, process monitoring, troubleshooting, and lifecycle management activities conducted by… more
    Otsuka America Pharmaceutical Inc. (10/17/25)
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  • Senior Director of API Manufacturing

    Kelly Services (South San Francisco, CA)
    Kelly(R) Science & Clinical is seeking an Associate Director / Director of Drug Substance Manufacturing for a direct hire opportunity with a leading ... Senior Director , $275,000 - $320,000 **Overview** As Associate Director / Director , Drug...you will be a strategic leader in drug substance process development, technology transfer, and external partnership management across… more
    Kelly Services (09/30/25)
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  • Director of Operations, Bio Supplies…

    Grifols Shared Services North America, Inc (Vista, CA)
    …manufacturing site goals and objectives; track and evaluate the critical process data to recommend continuous improvement throughout the organization. * Propose ... Thorough knowledge of FDA and international regulatory, quality and cGMP regulations + Demonstrated leadership skills with ability to...an equivalency could include 8 years of experience, an Associate 's degree with 6 years of experience, or a… more
    Grifols Shared Services North America, Inc (10/22/25)
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