• Supervisor, Quality Assurance

    Curia (Hopkinton, MA)
    …biotechnology or related field + Minimum 5 to 8 years' experience in Quality Assurance in the pharmaceutical /biotechnology or medical device industry experience, ... SUPERVISOR, QUALITY ASSURANCE in Hopkinton, MA Build your future...(CDMO) with over 30 years of experience partnering with pharmaceutical and biotech companies to provide life-saving treatments to… more
    Curia (05/31/25)
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  • Histology Associate - Pathobiology

    Eurofins (Boston, MA)
    …is accurate. Eurofins believes it is a global leader in food, environmental, pharmaceutical and cosmetics products testing and in agroscience CRO services. It is ... environment as well as other cross-functional project teams to provide timely, high- quality data to support the client. Key Duties & Responsibilities + Conduct… more
    Eurofins (05/28/25)
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  • Scientist, Analytical Development

    Sanofi Group (Framingham, MA)
    …seeking a highly motivated Scientist to join the Analytical Development and QC group within Mammalian Bioanalytics, located in Framingham, MA. The Analytical ... Development group has the overall responsibility to establish phase-appropriate control strategies and to develop, qualify, and validate robust analytical methods to… more
    Sanofi Group (05/25/25)
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  • Associate Director, Postmarketing PV Case…

    United Therapeutics (Boston, MA)
    …are as follows:** **Who we are** We are the first publicly-traded biotech or pharmaceutical company to take the form of a public benefit corporation. Our public ... a brighter future for patients through the development of novel pharmaceutical therapies; and technologies that expand the availability of transplantable organs.… more
    United Therapeutics (05/13/25)
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  • Senior Process Architect - Life Science…

    Burns & McDonnell (Newton, MA)
    **Description** The Senior Architect - Process will lead in the development of pharmaceutical and life science projects teams to create world-class designs for Life ... industry including but not limited to Animal Health, Biotechnology, and Pharmaceutical facilities. + Demonstrated ability to identify operational efficiency and… more
    Burns & McDonnell (03/07/25)
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  • Manager, Clinical Supply Operations

    Otsuka America Pharmaceutical Inc. (Boston, MA)
    …required. + Coordinate the release of clinical supplies with other functional groups (ie Quality Assurance and Quality Control ). + Coordinate QP release of ... in Life Sciences, Pharmacy or related scientific discipline + 3 years pharmaceutical industry experience + Some knowledge of GMPs (current Good Manufacturing… more
    Otsuka America Pharmaceutical Inc. (05/28/25)
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  • Sterility Assurance and Microbiology Global Expert

    Sanofi Group (Framingham, MA)
    …families. Your job as Sterility Assurance and Microbiology Global Expert within our Quality Control Microbiology team, will be to manage the global expertise ... is strongly preferred + Minimum of 15 years of industrial experience in Pharmaceutical /Biotech Sterile Manufacturing is required + Strong Quality mindset with… more
    Sanofi Group (05/28/25)
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  • Executive Director, Cell Therapy Global Product…

    Bristol Myers Squibb (Devens, MA)
    …of the Product Strategic Plan including, but not limited to: Global Change Control Strategies, Annual Product Quality Reviews, Product Life Cycle initiatives, ... . **Position Summary** The Executive Director, Cell Therapy Global Product Quality (CTGPQ) is responsible for development and implementation of all … more
    Bristol Myers Squibb (05/25/25)
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  • Associate Scientist I

    Charles River Laboratories (Worcester, MA)
    …analysis of samples by mass spectrometry, review/interpret bioanalytical results, and prepare/ QC data summaries under the guidance of more senior staff members. ... our client's unique challenges. Our client base includes global pharmaceutical companies, biotechnology companies, government agencies and hospitals and academic… more
    Charles River Laboratories (05/21/25)
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  • Clinical Trial Associate (CTA)

    US Tech Solutions (Cambridge, MA)
    …Ipsen e-TMF process and resolving issues related to missing documentation + Performing QC checks on TMFs to ensure completeness and readiness for audit/inspection + ... relevant Ipsen study team members. + Coordinate the TMF Quality Check (per Ipsen SOP) with the CRO/Ipsen to...+ Experience **in clinical study environment** within **CRO or Pharmaceutical company.** + Knowledge of the clinical study environment… more
    US Tech Solutions (05/06/25)
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