• Associate Director, External Manufacturing…

    Merck (West Point, PA)
    …molded Device Components, Device Constituents, and Medical Devices used to deliver Pharmaceutical , Biologic, and Vaccine Products. Our team works with a "Safety ... Reliability, and Lifecycle Management). - Lead Periodic Business and Operations Review Meetings (with External Partner). . **Compliance:** Achieve compliance goals… more
    Merck (08/18/25)
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  • Director - Life Sciences Advisory - Patient…

    Guidehouse (New York, NY)
    …team provides program design, implementation, and monitoring services to pharmaceutical , biotechnology, and medical device, companies. We support our clients ... course of study. + 10 years of Life Sciences ( Pharmaceutical , Biotech, Specialty Pharma and/or Medical Technology) consulting experience...services. + Excellent attention to detail and ability to review work product of self and others and produce… more
    Guidehouse (08/18/25)
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  • Managing Consultant - Life Sciences Advisory…

    Guidehouse (New York, NY)
    …Guidehouse's Life Sciences practice is an engine of innovation, helping pharmaceutical , biotech, medical device, and diagnostic companies develop custom solutions ... or related course of study. + 5-7 years of Life Sciences ( Pharmaceutical , Biotech, Specialty Pharma and/or Medical Technology) consulting experience is required.… more
    Guidehouse (08/18/25)
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  • Associate Scientist II, Analytical Research…

    Catalent Pharma Solutions (St. Petersburg, FL)
    …with 3 plus years in an GMP analytical lab + Experience with common pharmaceutical equipment: UV/VIS, IR, AA, and Dissolution required. + Expertise in wet chemistry ... instruments such as HPLC/UHPLC and GC required. + Familiar with pharmaceutical software such as LIMS, TrackWise, Empower, preferred. + Vision requirements… more
    Catalent Pharma Solutions (08/16/25)
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  • Quality Engineer

    Teledyne (Miamisburg, OH)
    …research, deepwater oil and gas exploration and production, medical imaging and pharmaceutical research.​ We are looking for individuals who thrive on making an ... performance analysis and reporting (suppliers and customers); + Lead Material Review Board and disposition of Non-Conforming Materials. Your requirements: + Bachelor… more
    Teledyne (08/16/25)
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  • Quality Assurance Associate - Controls

    Glenmark Pharmaceuticals Inc., USA (Allentown, PA)
    …proper documentation control activities are being followed per cGMP requirements + Review and maintaining existing Quality System and ensuring compliance to Agency ... + Minimum 1 to 5 years of related experience in the pharmaceutical industry, handling controlled substance, QMS, Warehouse compliance and Inspection activity.… more
    Glenmark Pharmaceuticals Inc., USA (08/16/25)
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  • Maintenance Manager

    Nestle (Anderson, IN)
    …+ Competent design knowledge. AutoCAD knowledge. + Project Management in the pharmaceutical or food industry. + Process qualification, validation in the ... pharmaceutical or food industry IQ, OQ, PQ. + Knowledge...###. This position is not eligible for Visa Sponsorship. Review our applicant privacy notice before applying at https://www.nestlejobs.com/privacy.… more
    Nestle (08/16/25)
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  • Senior Engineer, Application Development…

    Cardinal Health (Baton Rouge, LA)
    …Engineer to support the Pricing applications under Revenue Management team in Pharmaceutical Segment. This position will work with the different business teams on ... Docker, Java, SQL, Oracle, Groovy. + Native understanding of Pharmaceutical Business Pricing Processes like Contracts, Customer Attachments, GPOs/Buying Groups,… more
    Cardinal Health (08/15/25)
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  • Outpatient Pharmacy Technician (Full time, evening…

    Penn Medicine (Lancaster, PA)
    …in compliance with department policies and procedures that provide optimal pharmaceutical care. ESSENTIAL FUNCTIONS:Qualified individuals must have the ability (with ... observed by the pharmacist. + Retrieve and interpret prescriptions; perform pharmaceutical calculations, taking into account patient and drug characteristics; enter… more
    Penn Medicine (08/15/25)
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  • Regulatory Affairs Director (R7-R8)

    Lilly (Indianapolis, IN)
    …of regulatory projects for gene therapy platforms. Draft and review regulatory applications, supplements, amendments, and variations. Communicate regulatory ... of progressively responsible experience with supporting regulatory affairs for pharmaceutical development projects and marketed products. Experience must include a… more
    Lilly (08/15/25)
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