• Aequor (Pearl River, LA)
    …School degree with at least 2 years of work experience, or training within a cGMP manufacturing environment General knowledge of cGMP , GDP, SOP's Good ... Substance in the media, buffer and solution preparation areas of the cGMP commercial manufacturing facility. Requires good documentation skills and attention… more
    HireLifeScience (12/30/25)
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  • cGMP Vector Manufacturing

    University of Southern California (Los Angeles, CA)
    …Medicine, current Good Manufacturing Practices ( cGMP ) facility is seeking a qualified cGMP Vector Manufacturing Associate to join the USC/CHLA ... documentation of all reagents in accordance with established protocols. In addition, the cGMP Vector Manufacturing Associate will be responsible for the… more
    University of Southern California (12/23/25)
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  • cGMP Quality Control Associate

    University of Southern California (Los Angeles, CA)
    …Minimum Skills: Proficiency in operating and maintaining laboratory equipment used in cGMP manufacturing and quality control testing. Strong attention to detail ... it is. USC's Keck School of Medicine, current Good Manufacturing Practices ( cGMP ) facility is seeking a...Practices ( cGMP ) facility is seeking a qualified cGMP Quality Control Associate to join the… more
    University of Southern California (12/23/25)
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  • Manufacturing Associate II - 2nd…

    ThermoFisher Scientific (Plainville, MA)
    …rare, and untreatable diseases. **How will you make an impact?** As a second shift Manufacturing Associate II, you will play a crucial role in our ... Able to lift 40 lbs. without assistance, Adherence to all Good Manufacturing Practices (GMP) Safety Standards, Laboratory Setting, Some degree of PPE (Personal… more
    ThermoFisher Scientific (12/25/25)
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  • Associate Director, Genomic Medicine…

    Sanofi Group (Waltham, MA)
    …Strong technical background in AAV purification process + Experience with AAV cGMP Manufacturing , especially in purification operations + Experience of engaging ... **Job Title:** Associate Director, Genomic Medicine Purification Process Development **Location:**...scientists and engineers responsible for the development of viral vector purification processes, technology transfer to manufacturing more
    Sanofi Group (11/05/25)
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