• Director , Quality

    Sysco (Rahway, NJ)
    …building a high-performing quality culture across the organization. **POSITION PURPOSE:** The Director of Global Quality Assurance & Quality Control ... continuity across the entire supply chain-from development through delivery. ** Global Quality Strategy & Leadership** + Define...in domestic and international markets. + Stay current on global regulatory trends; assess potential impact and… more
    Sysco (09/05/25)
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  • Clinical Director

    Insight Global (Hackensack, NJ)
    …leadership for all clinical functions of the ASC. They ensure high- quality , patient-centered care; compliance with federal, state, and accreditor standards; and ... coordination among nursing, anesthesia, surgical, and support staff. The Clinical Director partners with the Administrator on budgeting, staffing, and performance… more
    Insight Global (09/25/25)
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  • Senior Director , Site Quality Head,…

    Teva Pharmaceuticals (Parsippany, NJ)
    Senior Director , Site Quality Head, Goa Date: Sep 5, 2025 Location: Parsippany, United States, New Jersey, 07054 Company: Teva Pharmaceuticals Job Id: 63901 ... for Manufacturing, Packaging and Laboratory Operations to ensure a mature culture of quality , compliance with regulatory requirements and quality of… more
    Teva Pharmaceuticals (09/06/25)
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  • Associate Director , Inspection Readiness

    Bristol Myers Squibb (New Brunswick, NJ)
    …approach. **Key Responsibilities** * Monitor and assess global regulatory inspection outcomes, enforcement actions, quality and compliance metrics, ... strategies by providing expert guidance on the interpretation and application of global regulatory requirements, as required. * Develop and maintain strong… more
    Bristol Myers Squibb (09/24/25)
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  • GRA Device Lead (Associate Director )

    Sanofi Group (Morristown, NJ)
    …families. Your skills could be critical in helping our teams accelerate progress. The Global Regulatory Affairs (GRA) Device team is a globally diverse team ... department bridges the gap between technical development, manufacturing operations, and global regulatory authorities to ensure compliance while optimizing… more
    Sanofi Group (09/23/25)
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  • GRA Device Lead (Associate Director )

    Sanofi Group (Morristown, NJ)
    …families. Your skills could be critical in helping our teams accelerate progress. The Global Regulatory Affairs (GRA) Device team is a globally diverse team ... department bridges the gap between technical development, manufacturing operations, and global regulatory authorities to ensure compliance while optimizing… more
    Sanofi Group (09/20/25)
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  • GRA Device Lead ( Director )

    Sanofi Group (Morristown, NJ)
    …diagnostic products within the Sanofi portfolio of products. The team is part of the Global Regulatory Affairs, Regulatory CMC and Device Department within ... **Job Title:** GRA Device Lead ( Director ) **Location** : Morristown, NJ, Cambridge, MA, Framingham,...Global Research and Development. Sanofi's global regulatory affairs (GRA) function is comprised… more
    Sanofi Group (07/15/25)
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  • Associate Director , Quality…

    Merck (Rahway, NJ)
    … Quality Assurance oversight for computer system validation matters within the Global Development Quality organization and for the Company's Research & ... + Act as a liaison with respect to the Quality Management System and Compliance pillars of Global...Units, including external suppliers. + As required, participate in Regulatory Agency inspection activities. + As required, participate as… more
    Merck (09/24/25)
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  • Associate Director -Principal Medical…

    Sanofi Group (Morristown, NJ)
    … Global Medical writing and Document management serves to generate timely, high quality , cost effective and regulatory compliant documents. Our mission is to ... **Job Title:** Associate Director -Principal Medical Writer **Location:** USA, Remote. Proximity to...synergize and harness evolving technologies pushing the edge of regulatory writing. We are an innovative global … more
    Sanofi Group (09/06/25)
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  • Senior Director , Clinical Leader…

    J&J Family of Companies (Titusville, NJ)
    …via matrix interactions also includes individuals from project management, TA strategy, global regulatory affairs, finance, legal, quality assurance, ... clinical study reports and for the preparation and approval of essential documents for global regulatory filings. The CL will manage direct reports who are… more
    J&J Family of Companies (09/03/25)
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