• Associate Director, Submissions Content…

    Merck (Rahway, NJ)
    …Programs, FDA Regulations, IT Coordination, IT Operation, Pharmacovigilance, Policy Implementation, Regulatory Compliance, Regulatory Labeling , Regulatory ... Business Operations Lead is expected to understand the end-to-end regulatory submission process. The main focus will be on...industry experience, at least 6 of those in a regulatory and/or compliance area and experience with technical systems… more
    Merck (11/01/25)
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  • Associate Director, PV Sciences

    Taiho Oncology (Princeton, NJ)
    …Proposition: Embark on a transformative journey with Taiho Oncology as an Associate Director in PV Sciences. At the forefront of pharmacovigilance innovation, we ... on your experience in our rapidly evolving organization. Position Summary: The Associate Director, PV Sciences role will lead medical surveillance activities for… more
    Taiho Oncology (11/04/25)
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  • Associate Director, Clinical Supplies…

    Merck (Rahway, NJ)
    …portfolio of clinical trials. GCS is accountable for the planning, sourcing, labeling , packaging and delivery of clinical supplies to clinical sites globally. The ... (as a lead GCS Planning program representative) such as clinical development, regulatory , quality and other supply chain areas to negotiate timelines, strategies and… more
    Merck (11/20/25)
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  • Associate Director, US Medical…

    Bristol Myers Squibb (Princeton, NJ)
    …work and in their personal lives. Read more: careers.bms.com/working-with-us . The Associate Director, US Medical Neuropsychiatry position works in the US Medical ... points across US functional and commercialization areas to ensure alignment. The Associate Director will report to the Senior Director, US Medical Neuropsychiatry.… more
    Bristol Myers Squibb (10/30/25)
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  • Manufacturing Operator - Warehouse

    Integra LifeSciences (Plainsboro, NJ)
    …patient outcomes and set new standards of care. The **Manufacturing Operator/Warehouse Associate ** will verify and keep records of all incoming and outgoing ... inventory locations, and perform all associated transactions in ORACLE. The warehouse associate will perform all required duties in compliance with company policies,… more
    Integra LifeSciences (09/13/25)
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  • Clean Room Manufacturing Operator - Warehouse

    Integra LifeSciences (Plainsboro, NJ)
    …inventory locations, and perform all associated transactions in ORACLE. The warehouse associate will perform all required duties in compliance with company policies, ... and Drug Administration and DOT/IATA, ISO 13485, and other applicable regulatory agencies. **SUPERVISION RECEIVED** Under direct supervision of the Warehouse… more
    Integra LifeSciences (11/07/25)
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  • Cloud Infrastructure Engineer 2

    Public Consulting Group (Trenton, NJ)
    …Qualifications** + Experience with Valimail + Familiarity with DLP frameworks, sensitivity labeling , and regulatory controls (HIPAA, SOX, GDPR as applicable). + ... Cloud Practitioner (CLF-C02) + Microsoft 365 Certified: Messaging Administrator Associate (MS-203). + Microsoft Certified: Azure Administrator Associate more
    Public Consulting Group (11/20/25)
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  • Quality Inspector II - First Shift (10hr - Mon.…

    Integra LifeSciences (Plainsboro, NJ)
    …ISO 9001, ISO 13485, the medical device directive, and the other applicable regulatory agencies. Expectations are to be familiar with and able to measure critical ... * Perform line clearances and quality reviews in manufacturing, labeling , or other assigned areas during manufacturing activities. *...knowledge, skill, and/or ability required for this position. * Associate degree in science is preferred. * 2 to… more
    Integra LifeSciences (11/05/25)
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