• Associate Engineering Fellow, Process Engineering

    Takeda Pharmaceuticals (Cambridge, MA)
    …will be recognized as a technical resource/expert within SMPD and across Pharmaceutical Sciences and utilize their technical expertise to contribute across multiple ... plant and commercial-scale production, ensuring smooth technology transfer and process validation . + Has full accountability for all engineering aspects for complex… more
    Takeda Pharmaceuticals (07/31/25)
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  • Senior Quality Engineer I - Design & Reliability…

    Integra LifeSciences (Braintree, MA)
    …documentation such as product requirements, schematics, verification, and validation strategy/execution. + Coordinate, review and approve development documentation ... SPC programs with Manufacturing and Quality Control as a part of Process Validation and Design Transfer. + Maintains knowledge of and applies statistical analysis to… more
    Integra LifeSciences (08/08/25)
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  • Quality Engineer II - Design & Reliability…

    Integra LifeSciences (Braintree, MA)
    …documentation such as product requirements, schematics, verification, and validation strategy/execution. + Coordinate and review development documentation created ... SPC programs with Manufacturing and Quality Control as a part of Process Validation and Design Transfer. + Knowledgeable of and applies statistical analysis to… more
    Integra LifeSciences (06/07/25)
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  • Associate Director, Product Quality

    AbbVie (Waltham, MA)
    …agency regulations worldwide. Products include regulatory starting materials, Active Pharmaceutical Ingredients (API), Intermediates, and Drug Products produced by ... Operations Management, Regulatory, Operations, or Technical Support in a pharmaceutical setting. Required regulatory inspection experience with direct interaction… more
    AbbVie (07/11/25)
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  • Associate Director, MSAT, Upstream

    Otsuka America Pharmaceutical Inc. (Boston, MA)
    …compliance of upstream operations through effective technology transfer, validation support, process monitoring, troubleshooting, and lifecycle management activities ... trends, and propose process improvements. + Support process characterization and validation activities (PPQ) for upstream processes executed at CDMOs. + Evaluate… more
    Otsuka America Pharmaceutical Inc. (07/18/25)
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  • Clinical Data Manager

    Sumitomo Pharma (Boston, MA)
    Sumitomo Pharma Co., Ltd. is a global pharmaceutical company based in Japan with key operations in the US (Sumitomo Pharma America, Inc.), Canada (Sumitomo Pharma ... the electronic CRF, Data Management Plan, CRF Completion Guidelines, Data Validation Specification, Data Transfer Specifications, etc. + Assist in managingclinical… more
    Sumitomo Pharma (09/03/25)
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  • Lab Operations Specialist (PM Shift)

    Actalent (Milford, MA)
    …validated, commissioned, and closed out in time. Skills GMP, equipment validation , inventory control, vendor management, pharmaceutical industry, Lab equipment, ... Data entry Top Skills Details GMP,equipment validation ,inventory control,vendor management, pharmaceutical industry Additional Skills & Qualifications * High… more
    Actalent (09/03/25)
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  • Analytical Chemist

    Cambridge Isotope Laboratories, Inc. (Tewksbury, MA)
    …high technology markets. CIL's growing customer base spans academia, pharmaceutical , medical diagnostic and semiconductor industries enabling collaborations with ... market growth. CIL is a subsidiary of the Otsuka Pharmaceutical Group and has had consistent growth for over...data in a scientific way to support development and validation work under GMP guidelines and SOP's + Troubleshooting… more
    Cambridge Isotope Laboratories, Inc. (09/01/25)
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  • Senior Statistical Programmer FSP

    Cytel (Cambridge, MA)
    **Sponsor-dedicated:** Working fully embedded within one of our pharmaceutical clients, with the support of Cytel right behind you, you'll be at the heart of our ... you will be dedicated to one of our global pharmaceutical clients; a company that is driving the next...listings, and figures (TLFs) + Production and QC / validation programming + Generating complex ad-hoc reports utilizing raw… more
    Cytel (08/02/25)
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  • Senior Statistical Programmer FSP

    Cytel (Boston, MA)
    **Sponsor-dedicated:** Working fully embedded within one of our pharmaceutical clients, with the support of Cytel right behind you, you'll be at the heart of our ... you will be dedicated to one of our global pharmaceutical clients; a company that is driving the next...(ISS/ISE), utilizing SAS programming + Production and QC / validation programming + Generating complex ad-hoc reports utilizing raw… more
    Cytel (07/24/25)
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