• 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 (06/09/25)
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  • Associate Director , Viral Vector…

    Gilead Sciences, Inc. (Oceanside, CA)
    …Kite Pharma a Gilead Sciences Company has an opportunity for an experienced Associate Director of Downstream Manufacturing Operations at our Oceanside biologics ... the purification and the fill finish and packaging manufacturing teams. The Associate Director of Downstream Manufacturing will be responsible for coordination,… more
    Gilead Sciences, Inc. (07/31/25)
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  • Associate Director , QA Complaints

    Grifols Shared Services North America, Inc (San Diego, CA)
    …in more than 110 countries and regions. Grifols Diagnostic Solutions is seeking an Associate Director , QA Complaints to be part of our Quality Assurance team ... in San Diego, CA. The Associate Director , QA Complaints manages the Complaints...manages the Complaints Handling, Post Market Surveillance, and Vigilance process for Grifols Diagnostic Solutions for one or more… more
    Grifols Shared Services North America, Inc (05/13/25)
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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. (07/18/25)
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  • Associate Director Quality Assurance

    Takeda Pharmaceuticals (Thousand Oaks, CA)
    By clicking the "Apply" button, I understand that my employment application process with Takeda will commence and that the information I provide in my application ... deviation management, and annual product reviews, while driving compliance with cGMP and regulatory requirements. You will contribute in global and site-level… more
    Takeda Pharmaceuticals (06/11/25)
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  • Associate Director , MSAT, Upstream

    Otsuka America Pharmaceutical Inc. (Sacramento, CA)
    …skilled and experienced professional to join our organization as the Assoc. Director of Manufacturing Science and Technology (MSAT) for Upstream processes. This ... of upstream operations through effective technology transfer, validation support, process monitoring, troubleshooting, and lifecycle management activities conducted by… more
    Otsuka America Pharmaceutical Inc. (07/18/25)
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  • Associate Director , Data,…

    Gilead Sciences, Inc. (Foster City, CA)
    …OR + PhD and Two Years' Experience + Experience in pharmaceutical operations/ cGMP environment highly desirable. + Excellent knowledge of logistics operations within ... track record of driving supplier performance by partnering with suppliers and managing the process from the ideation of projects to the measuring of benefits. + Can… more
    Gilead Sciences, Inc. (05/17/25)
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