• cGMP Process Development

    University of Southern California (Los Angeles, CA)
    cGMP Process Development ( PD ) Specialized Laboratory TechnicianApply (https://usc.wd5.myworkdayjobs.com/ExternalUSCCareers/job/Los-Angeles-CA ... cell and gene therapies and other biological products for internal/external users. The cGMP Process Development ( PD ) Specialized Lab Technician at the… more
    University of Southern California (06/11/25)
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  • cGMP Process Development

    University of Southern California (Los Angeles, CA)
    cGMP Process Development ( PD ) SpecialistApply (https://usc.wd5.myworkdayjobs.com/ExternalUSCCareers/job/Los-Angeles-CA Health-Sciences-Campus/ cGMP - ... cell and gene therapies and other biological products for internal/external users. The Process Development ( PD ) Specialist is responsible for developing… more
    University of Southern California (06/09/25)
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  • Scientist I, Product Development

    Catalent Pharma Solutions (St. Petersburg, FL)
    …processing in a pharmaceutical, cGMP environment. + Strong knowledge of cGMP Regulatory requirements for process development , technical transfer, and ... Product Development ** contributes significantly to the successful timely development of new pharmaceutical products utilizing Softgel Formulation/ Process more
    Catalent Pharma Solutions (05/16/25)
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  • Manager, Quality Systems and Compliance

    Bristol Myers Squibb (Madison, NJ)
    …system. Supports and coordinates document periodic revisions as required within Product Development Quality. + Supports the Document Management program by ... process through the collection, documentation, and reporting of PD metrics. + Provides support for the PD... PD metrics. + Provides support for the PD Self-Inspection program by functioning as a… more
    Bristol Myers Squibb (06/11/25)
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  • Senior Manager, Upstream Process

    Catalent Pharma Solutions (Baltimore, MD)
    …different departments to make sure the process is successfully transferred from PD to cGMP manufacturing + Plan, develop, organize, and implement policies, ... **Job Title:** Sr. Manager Upstream Process Development **City:** Baltimore **State** :...: + Lead the client projects starting from the development and optimization toward cGMP manufacturing for… more
    Catalent Pharma Solutions (05/11/25)
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  • Senior Scientist, Downstream Processing

    Danaher Corporation (Westborough, MA)
    …for Cytiva is responsible for providing technical leadership to the Fast Trak Process Development Services (PDS) group by providing technical and scientific ... support for the execution of downstream PD and scale-up process for various biologics...modalities. This position is part of the Fast Trak Process Development Services located in Westborough, MA… more
    Danaher Corporation (06/05/25)
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  • Director , Product Development

    Catalent Pharma Solutions (San Diego, CA)
    …leader to join us as Director , Product Development . The Director , Product Development ( PD ) is responsible for providing operational, scientific ... **Title: Director Product Development ** **About Catalent San...problem statements for small molecule and peptide therapeutics. The Director will lead the PD team and… more
    Catalent Pharma Solutions (06/13/25)
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  • Specialist II, Form/Fill (Weekend AM Shift)

    Novo Nordisk (Bloomington, IN)
    …is a state-of-the-art facility where we have an integrated model from process and formulation to clinical and commercial biomanufacturing and drug product ... in accordance with regulatory, site, and client requirements. Manufacturing cGMP production activities include manual, semi-automated and automated inspection,… more
    Novo Nordisk (05/10/25)
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  • Engineering - Process Engineer II

    Fujifilm (College Station, TX)
    …The Process Engineer II, under the supervision of the Director of Engineering, will be responsible for performing engineering activities, new equipment/systems ... introduction support, infrastructure assessments, troubleshooting support and technical expertise for process equipment and site utilities on behalf of the different… more
    Fujifilm (05/30/25)
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  • Sr. Associate, Manufacturing 12 hour Shift…

    Amgen (New Albany, OH)
    …and Validation. + Collaborate with Quality, Mfg Managers, Plant Engineering, Process Development and Regulatory Compliance staff in cross-functional teams. ... **Basic Qualifications:** High school/GED + 4 years biotech or pharmaceutical manufacturing, process development or quality experience Or Associate's + 2 years… more
    Amgen (06/13/25)
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  • Manufacturing Manager (Device Assembly…

    Amgen (New Albany, OH)
    …and Packaging facility. Responsibility includes maintaining production in full cGMP compliance. Supervises, hires, and develops staff and ensures production ... + Evaluate and approve reports and protocols. + Ensure cGMP and CFR compliance of manufacturing areas. + Revise,...+ Revise, update, and review procedures + Coordinate the development and revision of SOPs. + Evaluate current manufacturing… more
    Amgen (06/13/25)
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  • Downstream/Upstream Manufacturing Technician

    Kelly Services (Houston, TX)
    …CAPA resolution with SME and quality teams. * Provide input and support to MSAT/ PD during development and scale up activities as necessary. * Support facilities ... calibration and preventative maintenance as part of the equipment control program . * Maintain company and client confidentiality * Communicate safety policies… more
    Kelly Services (05/22/25)
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