• cGMP Associate Director…

    University of Southern California (Los Angeles, CA)
    …gene therapies and other biological products for internal/external users. The Associate Director of Process Development ( cGMP ) is responsible for all ... aspects of operations related to the current Good Manufacturing Practices ( cGMP ) laboratory, including manufacturing and process development activities, in order… more
    University of Southern California (11/19/25)
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  • Associate Director , API…

    Takeda Pharmaceuticals (Thousand Oaks, CA)
    …is true to the best of my knowledge. **Job Description** **About the role** As Associate Director , API Process Engineering, you will be Takeda's global ... the "Apply" button, I understand that my employment application process with Takeda will commence and that the information...+ At least 5 years of experience in a cGMP manufacturing environment and at least 5 years of… more
    Takeda Pharmaceuticals (11/25/25)
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  • Associate Director , Global Product…

    Otsuka America Pharmaceutical Inc. (Sacramento, CA)
    **Job Summary** The Associate Director , Global Product Quality - Biologics is responsible for directing quality oversight of clinical and commercial products at ... way that is in accordance with regulatory expectations and applicable cGMP /GDP quality standards. This role will direct Biologics Quality Assurance support,… more
    Otsuka America Pharmaceutical Inc. (12/02/25)
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  • Associate Director , Technical…

    Charles River Laboratories (Northridge, CA)
    …at HemaCare, you will make a difference every day. **Job Summary** The Associate Director , Technical Excellence is responsible for oversight of Technical ... current Good Laboratory Practice (cGLP) and current Good Manufacturing Practice ( cGMP ) compliant Cell & Gene Therapy (C>) products.. Essential Responsibilities +… more
    Charles River Laboratories (11/19/25)
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  • Associate Director , IT Regulatory,…

    Bristol Myers Squibb (San Diego, CA)
    …aims to be the global leader in radiopharmaceuticals. **Job Description** The Assoc. Director , IT Regulatory, Clinical and Enterprise Systems is an integral part of ... this role, you will report directly to the Exec. Director , IT and be primarily responsible for implementing RayzeBio's...infrastructure. + Deliver on service level management scope and process with IT groups and/or vendor managed services, ie,… more
    Bristol Myers Squibb (11/08/25)
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  • Associate Director , Document…

    Gilead Sciences, Inc. (Santa Monica, CA)
    …implement the strategy for Document Control to drive sustained compliance of CGMP /GDP activities. + Develop and implement a comprehensive global document control ... trends and best practices in document control. + Identify opportunities for process improvement and innovation. + Implement changes to enhance the efficiency and… more
    Gilead Sciences, Inc. (11/04/25)
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  • Director , External Quality Strategy…

    Gilead Sciences, Inc. (Foster City, CA)
    …Description** Gilead Sciences PDM External Quality is currently seeking a leader at the Associate Director / Director level to lead a team of Quality ... must possess expertise in leading cross-functional business and quality process mapping, identifying improvements to existing business and quality processes… more
    Gilead Sciences, Inc. (11/22/25)
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