• Supply Chain Operator, Cell Therapy in

    Bristol Myers Squibb (Devens, MA)
    …maintaining material inventory accuracy using required systems and equipment. + Support process investigations & CAPAs. + Provide support and suggestions on special ... projects such as validation of Material Operations areas. Document & Work Review...logbooks & worksheets. + Review work throughout the work process and at completion, in order to ensure that… more
    Bristol Myers Squibb (01/21/26)
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  • Equipment Maintenance Technician

    Catalent Pharma Solutions (Chelsea, MA)
    …consumer, and Catalent employee.** **The Role:** + Provide support for validation , calibration, and preventative maintenance of all Good Manufacturing Practices ... set-up/change-over + Assist in design and implementation of engineering controls. Assist process engineers as needed + All other duties as assigned **The… more
    Catalent Pharma Solutions (01/07/26)
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  • Vice President, Corporate Quality

    Bristol Myers Squibb (Devens, MA)
    …Leadership Team. **Key Responsibilities** + Establishes and oversees a unified, process -centric Quality Management System (QMS) that spans the entire product ... performance and sustain improvement. + Builds and develops a cross-divisional Global Process Owner Network that will develop and sustain the QMS working… more
    Bristol Myers Squibb (12/18/25)
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  • Senior Manufacturing Extrusion Engineer

    Medtronic (Danvers, MA)
    …regulated industries + Knowledge of failure analysis techniques, material characterization, and process validation + Familiarity with FDA, ISO, and GMP ... + Devise and implement cost savings proposals related to extrusion process andwork flowimprovements. + Execute onprocess and equipment validations through… more
    Medtronic (01/08/26)
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  • Senior Director, Analytical Excellence

    Bristol Myers Squibb (Devens, MA)
    …+ Benchmark industry best practices and implement innovative approaches to process efficiency, regulatory compliance, and quality improvement + Monitor performance ... science, QC operations, or method lifecycle management within the pharmaceutical /biologics industry; leadership at a multi-site/global level preferred + Demonstrated… more
    Bristol Myers Squibb (01/08/26)
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  • Product Development Science & Technology Cell Line…

    AbbVie (Worcester, MA)
    …gaining world-class experience in one of the most dynamic organizations in the pharmaceutical industry. This is a reality for AbbVie AbbVie Co-Ops. The Science & ... Technology (S&T) organization within AbbVie Operations leads the optimization, validation , implementation, continuous improvement, and global technical support for… more
    AbbVie (11/06/25)
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  • QC Manager, Bioanalytical

    ThermoFisher Scientific (Plainville, MA)
    …, a division of Thermo Fisher Scientific. At VVS, we deliver from process development through commercial supply, offering the expertise and resources vital to help ... QC and analytical method transfer activities. Responsibilities include qualification, validation , and transfer of molecular and bioanalytical assays (including qPCR… more
    ThermoFisher Scientific (01/10/26)
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  • Senior Data Scientist - Computer Vision…

    Merck (Cambridge, MA)
    …function is an AI/ML-first approach to improving target and biomarker discovery, validation and selection and elucidating complex disease mechanisms. As Senior Data ... Bioinformatics, Computational Biology, Genetics & Genomics, Mathematics, Statistics, Physics, Pharmaceutical Science, or related STEM field with 0+ years… more
    Merck (01/09/26)
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  • Global Senior Manager Early Access Programs

    Sanofi Group (Cambridge, MA)
    …and optimize resource allocation + Provide continuous improvement and process simplification for organizational efficiency and effectiveness and excellence in ... global medical teams in eligibility determination, country selection and blueprint validation . set up stakeholders meeting per program from start until… more
    Sanofi Group (01/07/26)
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  • Senior Engineer - I&C Systems Design (Remote…

    GE Vernova (Boston, MA)
    …conceptual through preliminary and detailed design, fabrication, assembly, production test, validation test as well as site installation, start-up test, and ... system, and component requirements; interfaces, function, performance, design assurance process , qualification, standards, regulatory guidance, certification or licensing commitments,… more
    GE Vernova (01/03/26)
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