• Quality Engineer 2, Device Quality Operations

    GRAIL (Durham, NC)
    …United Kingdom. It is supported by leading global investors and pharmaceutical , technology, and healthcare companies. For more information, please visit grail.com ... existing processes. + Support qualifications & validation activities (IQ/OQ/PQ/TMV) + Support DHR review process + Support NCR, DAR & CAPA process + Support change… more
    GRAIL (09/19/25)
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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, ... NJ. * Draft, review , and revise non-disclosure, vendor, service, and commercial agreements...knowledge of contracting and legal procedures, particularly related to pharmaceutical contracts and nondisclosure agreements. Robert Half is the… more
    Robert Half Legal (09/18/25)
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  • Area Business Specialist, Neuroscience (IA/NE/KS)…

    J&J Family of Companies (Omaha, NE)
    …health for humanity. Learn more at https://www.jnj.com **Job Function:** Pharmaceutical Sales **Job Sub** **Function:** Sales - Neuroscience (Commission) **Job ... from various locations to apply and encourage you to review the following states where this opportunity is available:...+ A minimum of three (3) years of successful pharmaceutical , biologic / biotech or medical device sales experience… more
    J&J Family of Companies (09/17/25)
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  • Group Medical Director

    AbbVie (North Chicago, IL)
    …assets with similar MOA + Leads and guide the safety physicians on data review (clinical and beyond) and interpretations across assets with similar MOA + Proactively ... to effectively conduct safety surveillance + Responsible for safety surveillance for pharmaceutical / biological / drug -device combined products + Lead and set… more
    AbbVie (09/17/25)
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  • Quality Assurance Specialist

    Catalent Pharma Solutions (Greenville, NC)
    …QA Management, supporting and providing guidance to laboratory staff as assigned. + Review Quality documentation including but not limited to review of ... degree with 4 years of professional experience in the pharmaceutical industry, preferably with 2 years in a Quality...role. + At least 1 year of batch record review and on the floor quality assurance manufacturing support.… more
    Catalent Pharma Solutions (09/16/25)
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  • Quality Operations Drug Product: Associate

    Pfizer (Groton, CT)
    …This role will offer the opportunity to collaborate with partner lines across Pharmaceutical Sciences Small Molecule (PSSM), as well as with other groups within PSSM ... quality touchpoints in cleaning validation, master batch records, working batch records, review of executed batch records and final bulk material disposition. + Help… more
    Pfizer (09/14/25)
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  • Sr. Specialist, Supplier Quality Management

    Cardinal Health (San Juan, PR)
    …Qualification Program and Lifecycle Management of Suppliers for Cardinal Health Pharmaceutical Private Label, consisting of the following: (1) Risk Assessment ... sources to determine Supplier risk profiles. + Audit Program: Prepares and/or review audit reports, ensure adequacy of supplier responses to audit observations, and… more
    Cardinal Health (09/10/25)
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  • Associate Director, Contract Development

    Sanofi Group (Cambridge, MA)
    …that align with company objectives and present them to the Pricing Committee for review and approval. + Manage the timely and accurate preparation, review , ... + Maintain tracking database of contract terms and proposals. + Peer review colleagues' strategic recommendations. + Ad-hoc analyses and special projects as… more
    Sanofi Group (09/10/25)
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  • Program Manager, Global Technology Transfers

    West Pharmaceutical Services (Jersey Shore, PA)
    …resources on managing required PNR and deviation investigation + Compiling, review and approval of Technology Transfer Equivalence Protocol (document defining ... documentation, references, test procedures and acceptance criteria + Compiling, review and approval Technology Transfer Equivalence Protocol Summary Report and… more
    West Pharmaceutical Services (09/10/25)
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  • Sr Quality Specialist, Systems

    Endo International (Rochester, MI)
    …for the corporate Quality Index. Reviews or approves the Site Quality Review for complaint investigations and monitors complaints to ensure that potential field ... works with cross functional teams and recommends improvements Management Review + Coordinates and prepares metrics and materials for...plus a minimum of 6+ years' experience in the pharmaceutical industry OR + MS +4 years' relevant experience… more
    Endo International (09/09/25)
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