• Director /Sr. Director , R&D…

    Bausch + Lomb (Trenton, NJ)
    …to continue leading the advancement of eye health in the future. **Objectives** The Director /Sr. Director is a member of the R&D Global Portfolio and Project ... (eg Vision Care), as well as leadership/facilitation/ management of the new product development (NPD) governance board. The role ensures effective and consistent… more
    Bausch + Lomb (06/06/25)
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  • Senior Medical/Scientific Director

    AbbVie (Florham Park, NJ)
    …process for Phase I-IV or extensive knowledge of Pharmaceutical Development including compliance and regulatory requirements. Must possess excellent oral and ... title will be based on qualifications listed below. Purpose: The Senior Director provides specialist medical and scientific strategic and operational input into core… more
    AbbVie (05/09/25)
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  • Sr. Director , Cloud Enablement

    ADP (Roseland, NJ)
    …implementation of comprehensive cloud governance frameworks, including enforceable policies, regulatory compliance controls, and standards for consistency across ... **ADP is hiring a Sr. Director , Cloud Enablement** ADP is seeking a strategic...ISO 27001), with proven expertise in data protection and regulatory compliance . + Strong Design experience OOPS… more
    ADP (05/22/25)
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  • Senior Director , R&D Project Management

    BD (Becton, Dickinson and Company) (Franklin Lakes, NJ)
    …: Support lifecycle management of existing products, ensuring quality, regulatory compliance , and cost improvement. + **New Product Development** : Lead the ... **Job Description Summary** The Senior Director , Program Management Office (PMO), R&D for MDS...multifaceted organization comprising project and program managers from various product platforms and significantly influence the direction of virtually… more
    BD (Becton, Dickinson and Company) (03/15/25)
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  • Associate Director , External Manufacturing…

    Merck (Rahway, NJ)
    …Knowledge of lean principles, equipment design, and preventative maintenance. . ** Regulatory ** - Global regulations and compliance requirements governing ... Operations, Drug Delivery Systems and Devices within our Manufacturing Division (Associate Director ). This role serves as a Virtual Plant Manager - responsible for… more
    Merck (05/19/25)
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  • Senior Medical Director for Molecular…

    Bayer (Whippany, NJ)
    …minds to make a real difference, there's only one choice.** **Senior Medical Director for Molecular Imaging and Theranostics** The Senior Medical Director for ... with cross-functional stakeholders across Medical Affairs, R&D, Marketing and Regulatory Affairs to ensure scientific excellence, drive innovation, and support… more
    Bayer (06/05/25)
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  • Executive Director , Biologics Analytical…

    Merck (Rahway, NJ)
    …retaining diverse talent. + Extensive knowledge of and hands-on work in applying regulatory guidance and quality standards related to product release and safety. ... Scientists to deliver analytical solutions that enable and accelerate process and product development and manufacturing and ensure safety and quality of our… more
    Merck (05/02/25)
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  • Director , MSAT Validation & Digital

    J&J Family of Companies (Raritan, NJ)
    …stakeholders at all levels to convey validation strategies, progress, and outcomes. ** Regulatory Compliance :** + Stay abreast of industry regulations and ... design and implementation of advanced validation strategies and frameworks to ensure compliance with regulatory standards. + Identify opportunities for process… more
    J&J Family of Companies (06/06/25)
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  • Medical Director or Scientific…

    AbbVie (Florham Park, NJ)
    …*Position title will be based on qualifications listed below. Purpose: The Director provides specialist medical and scientific strategic and operational input into ... commercial teams to provide strategic medical input into core brand ( product ) strategies, and to support medical affairs, marketing activities (promotional material… more
    AbbVie (05/10/25)
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  • Associate Medical Director

    Sumitomo Pharma (Trenton, NJ)
    …Ad-Hoc Regulatory safety inquiries. + Represents PVRM on post-marketing product specific and/or clinical study team meetings and governance committees. + ... encounters is considered confidential. ** Compliance ** : Achieve and maintain Compliance with all applicable regulatory , legal and operational rules and… more
    Sumitomo Pharma (05/16/25)
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