• Technical Area Specialist - AP - EPR Form / w&s…

    Novo Nordisk (Clayton, NC)
    …for millions of people around the world. In NC, we operate three pharmaceutical manufacturing facilities that are responsible for fulfilling different steps in our ... 6 weeks paid family medical leave + Free access to Novo Nordisk-marketed pharmaceutical products + Tuition Assistance + Life & Disability Insurance + Employee… more
    Novo Nordisk (08/01/25)
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  • Senior Principal Scientist, Translational…

    Merck (South San Francisco, CA)
    …seeking a highly qualified physician-scientist with a proven track record in the pharmaceutical industry as well as independent academic research for a position in ... The preferred candidate will have at least 5-year experience in the pharmaceutical industry and Immunology R&D and clinical and academic expertise in… more
    Merck (07/31/25)
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  • Manufacturing Specialist (MES)

    Grifols Shared Services North America, Inc (Los Angeles, CA)
    …The successful candidate will have at least five years' experience in a pharmaceutical or biotech industry and will have demonstrated competency in a team ... (Supervisors, Operators, Technical/QA/Support staff). + Responsible for the development, review , and update of MES Standard Operating Procedures. + Responsible… more
    Grifols Shared Services North America, Inc (07/29/25)
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  • Data Integrity Compliance Coordinator

    ThermoFisher Scientific (Greenville, NC)
    …Coordinator ensures compliance with data integrity standards at the pharmaceutical manufacturing site by providing administrative and operational support within ... and approval of DI-related deviations, CAPAs, and change controls for QA review . Track status and timelines using the electronic quality system (eg, TrackWise).… more
    ThermoFisher Scientific (07/26/25)
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  • Analytical Chemist II

    Catalent Pharma Solutions (Greenville, NC)
    …performing routine and non-routine analytical testing in support of pharmaceutical products following all applicable safety, quality, and regulation requirements. ... science degree with 4 years of professional experience in pharmaceutical analytical chemistry or; + BS or BA degree...that is independent and proficient in chromatography and data review as well as troubleshooting and technical understanding may… more
    Catalent Pharma Solutions (07/24/25)
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  • Pharmacy Trade Relations Strategy Director…

    Prime Therapeutics (Boston, MA)
    …Trade Relations Strategy Director - remote **Job Description** The Pharmaceutical Trade Relations Strategy Director facilitates formulary strategy development and ... strategy related to the development and implementation of strategic initiatives concerning pharmaceutical manufacturers + Direct or manage a team of analysts to… more
    Prime Therapeutics (07/22/25)
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  • Associate Director, Medical Affairs Omnichannel

    Otsuka America Pharmaceutical Inc. (St. Paul, MN)
    …with deep experience in the ever-developing Omnichannel effort in the pharmaceutical industry with a focus on Medical Affairs initiatives. **Key Responsibilities:** ... standards. + Collaborate with Compliance and Legal to maintain robust review processes and documentation. + **Leadership & Innovation:** + Provide strategic… more
    Otsuka America Pharmaceutical Inc. (07/15/25)
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  • Quality Deviation Investigator III

    Curia (Albuquerque, NM)
    …organization (CDMO) with over 30 years of experience partnering with pharmaceutical and biotech companies to provide life-saving treatments to patients. At ... and manufacture. Education and Experience: + Bachelor's Degree in Engineering, Pharmaceutical Technology, Chemistry, Pharmacy, or related field of study + Minimum… more
    Curia (06/26/25)
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  • Infusion Pharmacy Technician Lead

    Sutter Health (Mountain View, CA)
    …and proper allocation of pharmacy resources. Provides timely and accurate pharmaceutical care. Prepares, compounds, packages, labels, and dispenses medication, IV ... person (DP) of the compounding facility per USP compounding chapters, review and improve standard operating procedure/policies related to sterile compounding and/or… more
    Sutter Health (06/26/25)
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  • R&D Senior Quality Specialist (Validation)

    AbbVie (Irvine, CA)
    …of validation activities, and preparation of validation documentation within Pharmaceutical Development, with established guidelines for pharmaceutical products ... GMP environment. + Utilize knowledge of GMP concepts relating to Pharmaceutical manufacturing environment to plan, develop, organize, and execute validation… more
    AbbVie (06/21/25)
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