• Associate , QC Analytical

    Bristol Myers Squibb (Devens, MA)
    …place than here at BMS with our Cell Therapy team. Bristol Myers Squibb is seeking an ** Associate , QC Analytical , Cell Therapy** to join our QC ... Cell Therapy Facility (CTF) in Devens, MA. The QC Associate is responsible for supporting ...QC Associate is responsible for supporting Quality Control bioanalytical testing for in-process, release,… more
    Bristol Myers Squibb (09/09/25)
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  • Senior Specialist, QC Materials Management,…

    Bristol Myers Squibb (Devens, MA)
    …new hope to patients, there's no better place than here at BMS with our Cell Therapy team. The **Senior Specialist, QC Materials Management** is responsible for ... the management of materials used in the analytical and microbiology QC laboratories in the...onboarding of new materials through document creation and change control , collaborating with QC network functions and… more
    Bristol Myers Squibb (09/09/25)
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  • Specialist, Quality Assurance Shop Floor,…

    Bristol Myers Squibb (Devens, MA)
    …and oversight of site operations, including but not limited to Manufacturing, Quality Control laboratories, and Warehouse Operations. The **Specialist, QA Shop ... no better place than here at BMS with our Cell Therapy team. The Quality Assurance Shop...procedures, and practices. + Review manufacturing batch records or QC testing records to ensure compliance with approved procedures.… more
    Bristol Myers Squibb (09/10/25)
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  • VBU Product Operations, Associate

    Takeda Pharmaceuticals (Boston, MA)
    …assays, assay automation highly desirable. + Familiarity with working within fast paced, Quality Control laboratories highly desirable. + Be well organized and ... Takeda Vaccines is looking for a VBU Product Operations, Associate to join our Cambridge, MA office. + Perform...our Cambridge, MA office. + Perform routine assays involving cell culture, immunoassays, RNA/DNA isolation, and PCR independently in… more
    Takeda Pharmaceuticals (08/27/25)
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  • Associate

    US Tech Solutions (Cambridge, MA)
    …and CE method qualification studies to support transfer of methods to pivotal Quality Control teams. + Perform forced degradation studies to support product ... within the Process Development (PD) organization defines the favorable quality characteristics of the therapies it produces, and optimizes state-of-the-art… more
    US Tech Solutions (09/06/25)
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