• Director of Pharmacy Benefit Manager Oversight

    State of Massachusetts (Boston, MA)
    …of individual Pharmacy Benefit Manager practices. * Monitor market trends in pharmaceutical benefits in collaboration with staff from the Health Care Access Bureau ... ad hoc data calls and research reports in response to emerging pharmaceutical benefit issues. Prepare periodic and annual reports, including those specified by… more
    State of Massachusetts (12/04/25)
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  • Validation Engineer III

    ThermoFisher Scientific (Frederick, MD)
    …ear plugs etc.) **Job Description** **Division Specific Information** CTD partners with pharmaceutical and biotech customers around the world to ensure the right ... or equivalent validation experience including five years of food or pharmaceutical packaging or cGMP experience **Minimum Qualifications:** + Knowledge of Computer… more
    ThermoFisher Scientific (12/04/25)
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  • Regulatory Affairs Associate Director, IVD

    GRAIL (Albany, NY)
    …United Kingdom. It is supported by leading global investors and pharmaceutical , technology, and healthcare companies. For more information, please visit grail.com ... affairs, quality, or program management within the IVD, medical device, or pharmaceutical industries is required. + Regulatory affairs and IVD device experience… more
    GRAIL (12/03/25)
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  • Senior Client Partner / Sales Representative…

    Oracle (Lansing, MI)
    …Evidence (RWE), Clinical, Regulatory, and Safety research services** within pharmaceutical and biotechnology organizations. This role is responsible for identifying, ... account-specific business plans and sales strategies for a defined portfolio of pharmaceutical and biotech clients. + Own the full sales cycle including pipeline… more
    Oracle (12/03/25)
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  • Senior Manager, Global Product Quality - Biologics

    Otsuka America Pharmaceutical Inc. (Baton Rouge, LA)
    …Biology, Engineering or related Science. + Four years of combined experience in pharmaceutical /medical device industry as a manager in Manufacturing, QA or QC role ... Center at: https://www.ic3.gov , or your local authorities. Otsuka America Pharmaceutical Inc., Otsuka Pharmaceutical Development & Commercialization, Inc., and… more
    Otsuka America Pharmaceutical Inc. (12/03/25)
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  • Process Operator

    Catalent Pharma Solutions (Malvern, PA)
    …Process Operator micronize\mills client provided material including both active pharmaceutical ingredients and excipients as per Catalent Micron Technologies ... **The Role** + Micronization and milling of both hazardous and non-hazardous pharmaceutical actives and excipients. + Set up, operate equipment, and monitor… more
    Catalent Pharma Solutions (12/03/25)
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  • Senior Mechanic, Maintenance - DPF

    United Therapeutics (Stewartville, MN)
    …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 (12/03/25)
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  • Manager / Associate Principal, Insights…

    Blue Matter (San Francisco, CA)
    …insights CoE, uniquely combining sophisticated quantitative analytics with strategic pharmaceutical consulting. BMI consultants work side-by-side with strategy team ... 6-10 years of quantitative analytical experience in life sciences consulting, pharmaceutical industry, or healthcare analytics + Deep expertise in pharmaceutical more
    Blue Matter (12/03/25)
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  • Associate Director, R&D Strategic Sourcing,…

    Otsuka America Pharmaceutical Inc. (Princeton, NJ)
    …in R&D sourcing or formal supplier management roles within the pharmaceutical industry, supporting R&D functions. Apply supplier management principles, practices, ... Center at: https://www.ic3.gov , or your local authorities. Otsuka America Pharmaceutical Inc., Otsuka Pharmaceutical Development & Commercialization, Inc., and… more
    Otsuka America Pharmaceutical Inc. (12/03/25)
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  • Technical Documentation Specialist

    Kelly Services (St. Louis, MO)
    …manufacturing of critical infection prevention cleaning chemistries in a dynamic pharmaceutical environment. **What You'll Do:** + Develop, edit, and maintain ... **What You'll Bring:** + Proven experience in a GMP-regulated pharmaceutical manufacturing environment. + Expertise in navigating, updating, and developing… more
    Kelly Services (12/03/25)
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