• Associate Director, Market Research…

    Organon & Co. (Jersey City, NJ)
    …is achieved through close collaboration with key stakeholders in Commercial, Legal, Compliance , Privacy, Procurement, Business Technology, Quality & Audit, and ... packages, due-diligence processes, record keeping, and reporting to Pharmacovigilance compliance ; maintenance of the Pharmaceutical Master File information… more
    Organon & Co. (11/04/25)
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  • Senior Manager, Compliance

    Glenmark Pharmaceuticals Inc., USA (Elmwood Park, NJ)
    …understanding of laws and regulations, enforcement actions and evolving practices relevant to pharmaceutical compliance and works with CCO to make updates to ... to compliance is preferred Experience + Prior pharmaceutical compliance experience required. + Mastery of...development and commercialization of generic drugs of the highest quality and value. We help to improve people-s lives… more
    Glenmark Pharmaceuticals Inc., USA (10/31/25)
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  • Associate Director, Centralized Compliance

    J&J Family of Companies (Raritan, NJ)
    …and execution of Johnson & Johnson Technology Services (JJT-TS) and Enterprise Quality (EQ) core compliance programs for Regulatory Standards Management, ... highly preferred **Required:** + 7+ years of experience in managing all aspects of Quality and Regulatory Compliance in an international, global context, in a… more
    J&J Family of Companies (11/18/25)
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  • Senior Director, Compliance & Ethics,…

    Teva Pharmaceuticals (Parsippany, NJ)
    Senior Director, Compliance & Ethics, Global R&D Date: Nov 22, 2025 Location: Parsippany, United States, New Jersey, 07054 Company: Teva Pharmaceuticals Job Id: ... opportunity** The individual will serve as a strategic business partner and compliance advisor to all global R&D functions (which includes Global Medical Affairs,… more
    Teva Pharmaceuticals (09/25/25)
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  • Senior Director, Site Quality Head, Goa

    Teva Pharmaceuticals (Parsippany, NJ)
    …you'll spend your day** + Leads the Quality organization on site including Quality Control, Microbiology, Quality Compliance , Quality Systems and ... and Laboratory Operations to ensure a mature culture of quality , compliance with regulatory requirements and ...or Pharmacy Key Requirements: + Minimum of 10 years pharmaceutical manufacturing site quality operations and leadership… more
    Teva Pharmaceuticals (09/06/25)
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  • Director, Quality Assurance PV

    Taiho Oncology (Princeton, NJ)
    …of QA, PV and PV colleagues to assure their strategy and execution ingrains quality and compliance across all aspects of product safety across clinical ... teams and independently prioritize work, manage multiple projects while maintaining quality and advocating compliance . + Strong understanding of clinical… more
    Taiho Oncology (11/14/25)
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  • Lead Associate, Quality Audits

    Dr. Reddy's Laboratories (Princeton, NJ)
    …sites, internal GMP (Good Manufacturing Practices) departments, external partners, and quality systems for ensuring compliance with regulatory requirements and ... and continuous improvement. The role will report to Lead, Quality & Compliance . **Roles & Responsibilities** +...work experience:** 8+ years of progressive experience in auditing pharmaceutical or medical device systems, including 2 years of… more
    Dr. Reddy's Laboratories (11/05/25)
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  • Compliance Specialist

    Schlesinger Group (Iselin, NJ)
    …will be provided to our selected candidate at hiring time. As a Compliance Specialist, you will support our organization's commitment to ethical standards and ... regulatory compliance in the healthcare market research industry. This role...ensure adherence to industry codes (eg, BHBIA, EphMRA, and pharmaceutical marketing codes). + Partner with cross-functional teams-including Legal,… more
    Schlesinger Group (11/26/25)
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  • Compliance Investigator

    Actalent (Allendale, NJ)
    …2-3 years of experience writing and reviewing deviations and investigations within a pharmaceutical company. + Experience working with quality assurance teams to ... responsible for writing and completing investigations and deviations from a compliance and operations perspective. This role involves conducting root cause analyses… more
    Actalent (11/19/25)
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  • Labs FSP - Laboratory Compliance

    ThermoFisher Scientific (New Brunswick, NJ)
    …5 years experience in GMP environment - either laboratory setting, manufacturing, or quality / compliance . Experience in training management is a must and writing ... digital and decentralized clinical trial services. Your determination to deliver quality and accuracy will improve health outcomes that people and communities… more
    ThermoFisher Scientific (11/28/25)
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