• Director, Engineering & Maintenance

    Curia (Albuquerque, NM)
    …where our work has the power to save lives Curia is a global contract development and manufacturing organization (CDMO) with over 30 years of experience partnering ... with pharmaceutical and biotech companies to provide life-saving treatments to...oversees all environmental, health, and safety initiatives to ensure compliance with applicable regulatory agency requirements and internal company… more
    Curia (06/11/25)
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  • Sr. Director Research - Administration - Full Time

    Guthrie (Sayre, PA)
    …and monitor program budgets, grant revenue, and research-related expenses. + Manage pharmaceutical and federally funded study contracts, billing compliance , and ... a senior administrative executive to collaboratively lead the strategic, operational, and compliance functions of DGF. This role is central to ensuring the effective… more
    Guthrie (05/14/25)
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  • Senior Site Contracting Manager

    J&J Family of Companies (Titusville, NJ)
    …to clinical trials and/or overseeing a Clinical Research Organization responsible for contract negotiations. Provide support to the clinical team in the pricing, ... sites or via oversite of a Clinical Research Organization responsible for contract negotiations. + the delivery on established targets/measurements. + analyzing … more
    J&J Family of Companies (07/31/25)
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  • Project Manager

    Catalent Pharma Solutions (San Diego, CA)
    **Project Manager** **Position Summary:** Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to develop, ... annually. Catalent Pharma Solutions in San Diego is a premier pharmaceutical chemistry development and manufacturing organization supporting the pharmaceutical more
    Catalent Pharma Solutions (08/02/25)
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  • Project Manager

    Catalent Pharma Solutions (Greenville, NC)
    …is a global, high-growth, public company, and a leading partner for the pharmaceutical industry in the development and manufacturing of new treatments for patients ... is committed to a Patient First culture through excellence in quality and compliance , and to the safety of every patient, consumer and Catalent employee. Catalent's… more
    Catalent Pharma Solutions (07/12/25)
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  • Quality Control Analyst III

    Curia (Camarillo, CA)
    …data summaries to management + Utilize a thorough understanding of regulatory and compliance guidelines for the pharmaceutical industry + Interact with other ... the power to save lives. Curia is a global contract development and manufacturing organization (CDMO) with over 30...(CDMO) with over 30 years of experience partnering with pharmaceutical and biotech companies to provide life-saving treatments to… more
    Curia (06/17/25)
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  • Government Contracts Manager

    Teledyne (Torrance, CA)
    …research, deepwater oil and gas exploration and production, medical imaging and pharmaceutical research.​ We are looking for individuals who thrive on making an ... starting from proposal development, negotiations, order entry, program execution and through contract closeout. The person in this position will have an attention to… more
    Teledyne (07/29/25)
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  • Paralegal

    Robert Half Legal (Mahwah, NJ)
    Description Our client, a research-led, innovative, global pharmaceutical company, is looking for a senior corporate paralegal to join their team in Elmwood Park, ... the direction and supervision of attorneys. * Draft, review, and prepare contract templates. * Draft, review, and revise legal presentations, training materials, and… more
    Robert Half Legal (07/08/25)
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  • Sr Manager, Commercial Contracting

    Gilead Sciences, Inc. (Foster City, CA)
    …data subject matter expert to ensure proper data validation, verification of contract compliance , rebate processing. **Job Description:** + Ability to manage ... management and processing of all Managed Care Commercial/Medicare Part D contract payments. This position has primary ownership of maintaining strong relationships… more
    Gilead Sciences, Inc. (07/16/25)
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  • Quality Specialist I

    Element Materials Technology (Santa Fe Springs, CA)
    …and work effectively as part of a team + Experience in a pharmaceutical or analytical contract laboratory setting. + Familiarity with electronic quality ... the Quality Assurance function by performing routine QA activities to ensure compliance with applicable regulatory requirements (eg, FDA 21 CFR Part 11, 210/211,… more
    Element Materials Technology (07/24/25)
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