• Associate Director, MSAT, Upstream

    Otsuka America Pharmaceutical Inc. (Boston, MA)
    …review, gap analysis, and risk assessment. + Provide expert technical oversight of upstream manufacturing operations at CDMOs, including review of batch records, ... to join our organization as the Assoc. Director of Manufacturing Science and Technology (MSAT) for Upstream ...of Manufacturing Science and Technology (MSAT) for Upstream processes. This critical role will lead our efforts… more
    Otsuka America Pharmaceutical Inc. (07/18/25)
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  • Manufacturing Associate

    Sanofi Group (Framingham, MA)
    **Job Title:** Manufacturing Associate **Location:** Framingham, MA **Hours:** This is a 12-hour, Night-time (7:00 pm-7:00 am), rotating position **About the ... Operational Commissioning/Shakedown through process validation (PV) and commercial operations. The Manufacturing Associate will be responsible for performing a… more
    Sanofi Group (06/27/25)
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  • Automation Manufacturing Engineer

    Danaher Corporation (Shrewsbury, MA)
    …Alignment and Readiness: Understand and improve automation processes to ensure manufacturing readiness for upstream bioprocessing hardware. + Product Quality ... Business System (https://www.danaher.com/how-we-work/danaher-business-system) which makes everything possible. The Automation Manufacturing Engineer resolves daily operational challenges, engages in strategic… more
    Danaher Corporation (07/15/25)
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  • Associate Director, MSAT, Downstream Drug…

    Otsuka America Pharmaceutical Inc. (Boston, MA)
    **Job Summary** **​** The Associate Director, MSAT - Downstream provides specialized technical leadership and oversight for all downstream manufacturing ... and risk assessment. + Provide expert technical oversight of downstream manufacturing operations at CDMOs, including review of batch records, deviation… more
    Otsuka America Pharmaceutical Inc. (07/18/25)
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  • Engineer II, Process Development

    Takeda Pharmaceuticals (Lexington, MA)
    …individual will be a member within a group responsible for performing upstream and downstream related process development activities, including timely completion of ... bring new biopharmaceutical products to pre-clinical, clinical and process validation manufacturing phases. Under supervision, the scope of work includes cell… more
    Takeda Pharmaceuticals (07/19/25)
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