• Novo Nordisk Inc. (Plainsboro, NJ)
    …of Clinical, medical, Regulatory (CMR) Business Operations, the Associate Director (AD) is responsible for structuring facilitating and monitoring external-facing ... budgeting guidance. Collaborating with cross-functional teams to ensure contractual compliance and driving continuous improvement. Works closely with suppliers to… more
    HireLifeScience (01/11/25)
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  • Genmab (Plainsboro, NJ)
    …development.Oversee resource allocation and ensure effective team planning.Regulatory and Audit ComplianceEnsure compliance with country-specific clinical supply ... is essential to fulfilling our purpose.The RoleGenmab is searching for an experienced Director , Global Clinical Drug Supply to be part of Global Clinical Drug Supply… more
    HireLifeScience (01/07/25)
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  • Director , Compliance

    Hackensack Meridian Health (Belle Mead, NJ)
    …to transform healthcare and serve as a leader of positive change. The ** Director , Compliance and Risk Audit ** assists the Compliance Officer in the ... **Responsibilities** A day in the life of a ** Director , Compliance and Risk Audit ** at **Hackensack Meridian** **_Health_** includes: + Corporate … more
    Hackensack Meridian Health (01/23/25)
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  • Director IT Audit

    Highmark Health (Trenton, NJ)
    …for the technology component of the comprehensive, risk -based information systems audit , advisory, and compliance plan for the Highmark Health enterprise ... with senior operational and technology business leaders, ensures that the respective risk management and compliance programs address applicable laws, rules,… more
    Highmark Health (01/16/25)
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  • Senior Director , Clinical Quality…

    Bristol Myers Squibb (Princeton, NJ)
    …and external vendors to promote a culture of quality, risk management and compliance excellence. The Senior Director will also play a crucial role in ... with RGO and cross functional business partners to identify areas of greatest compliance risk and obtain information and feedback relevant to process improvement… more
    Bristol Myers Squibb (01/25/25)
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  • Associate Director , GCP Compliance

    Takeda Pharmaceuticals (Trenton, NJ)
    …company to inspire you and empower you to shine? Join us as an Associate Director , GCP Compliance based remotely reporting to the Director , GCP ... development of applicable processes and tools + Establish and lead proactive risk -based compliance assessments for clinical trial delivery functions and ensure… more
    Takeda Pharmaceuticals (11/14/24)
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  • Director , Compliance and Ethics…

    Bristol Myers Squibb (Princeton, NJ)
    …be recognized internally and externally as an expert in mitigating healthcare compliance risk through providing advice, drafting policy, providing education and ... Reporting to the Head of US and Above Market Compliance and Ethics Organization, this role partners with senior...Legal, Commercial, Medical, R&D, Global Drug Development, Regulatory, IT, Audit , Finance and HR to build and integrate one… more
    Bristol Myers Squibb (01/23/25)
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  • Associate Director , Therapeutic Area…

    Bristol Myers Squibb (Princeton, NJ)
    …personal lives. Read more: careers.bms.com/working-with-us . **Position Summary** The Associate Director , Therapeutic Area Audit Strategy Lead will be mainly ... of the Quality Narrative, specifically developing and contribution the audit /inspection portion . + Apply a risk -based...the central QMS team + Lead the Quality and Compliance R&D Escalation Process + Ensure GLP systems are… more
    Bristol Myers Squibb (01/25/25)
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  • Associate Director , Specialty Laboratory…

    Bristol Myers Squibb (Princeton, NJ)
    …vendor quality oversight: + Provide direction and oversight to the vendor qualification and audit program to ensure regulatory compliance + Develop the audit ... laboratory vendor audits, including audit scope to assess the vendors risk , quality systems, capabilities and performance + Supports the development of clinical… more
    Bristol Myers Squibb (01/25/25)
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  • Associate Director , Specialty Lab QA

    Bristol Myers Squibb (Princeton, NJ)
    …Quality is responsible for effective management of the GLP/GCLP/GCP specialty laboratory audit program, with an emphasis on risk -based management, regulatory ... and identify solutions. + Assist in managing the LQA audit program, including development of audit strategy...compliance : + Compile documentation in preparation for the audit . + Maintain NCQ audit database, perform… more
    Bristol Myers Squibb (01/25/25)
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  • ESG Accounting & Internal Controls Director

    Amneal Pharmaceuticals (Bridgewater, NJ)
    Description: The Director , ESG Accounting and Internal Controls will lead the development, implementation, and oversight of our Environmental, Social, and Governance ... data, manage the ESG internal control environment, and drive regulatory compliance across ESG disclosures. This position will partner closely with cross-functional… more
    Amneal Pharmaceuticals (12/26/24)
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  • Associate Director , Postmarketing PV Case…

    United Therapeutics (Trenton, NJ)
    …other orphan diseases. **How you'll contribute** The Associate Global PV Case Management Director plays a key role in management and oversight of end-to-end case ... commercial product portfolio. This position strategizes and implements plans to ensure compliance with global regulations and guidelines with regards to safety data… more
    United Therapeutics (12/14/24)
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  • Associate Director , Global Labeling Lead…

    Takeda Pharmaceuticals (Trenton, NJ)
    …to bring life-changing therapies to patients worldwide. Join Takeda as Associate Director , Global Labeling Lead where you will be responsible for the development ... CCDS, USPI and EU SmPC enabling the most up-to-date information and in compliance with labeling requirements to be provided to patients and Health Care Providers… more
    Takeda Pharmaceuticals (01/15/25)
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  • HSE Director

    Hovione (East Windsor, NJ)
    …is why we are In it for life. You will be responsible to: Independent compliance function within HSE focused on the development and implementation of an internal ... audit methodology to monitor and report on management system...applications. - To develop and implement a Chemical Hazard Risk Control program. - To drive the development and… more
    Hovione (11/19/24)
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  • Supply Chain Solutions Director

    Intermountain Health (Trenton, NJ)
    …procedures, guidelines, contracts and standards for assigned service line(s). Collaborates with Audit to ensure compliance . Manages requests for product standard ... business to establish and manage strategic supplier goals. Monitor supply risk contracted suppliers in portfolio. Drives continuous improvement plans with suppliers.… more
    Intermountain Health (01/21/25)
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  • Sr. Microbiologist, CMC

    Integra LifeSciences (Plainsboro, NJ)
    …to help improve outcomes. **SUMMARY** Under the direct supervision of the Director , Quality Reliability Microbiology, this individual will have a dotted line ... environments is required. The qualified candidate must understand the concepts of risk management as it relates to microbial monitoring and sterility assurance in… more
    Integra LifeSciences (12/30/24)
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  • Dir, Analytical R&D

    Merck (West Point, PA)
    …development and manufacturing and ensure safety and quality of our products. As Director of the Vaccines Analytical Research and Development (V-AR&D) GxP team, you ... The successful candidate will be accountable for proactive resourcing planning, risk assessment strategies and will focus on talent development and partnering… more
    Merck (01/17/25)
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