• Sr. Scientist Peptides API EM

    Lilly (Branchburg, NJ)
    …contract manufacturers. The position requires knowledge of cGMPs, applicable global regulatory manufacturing guidance, and the corporate/industry standards. ... to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work… more
    Lilly (08/08/25)
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  • Associate Medical Director, PVRM

    Sumitomo Pharma (Trenton, NJ)
    …of drug development in the pharmaceutical industry, including clinical research and global regulatory requirements + Experience managing safety data, expedited ... Sumitomo Pharma Co., Ltd. is a global pharmaceutical company based in Japan with key...Safety Charters + Handles Health Hazard Evaluations and Ad-Hoc Regulatory safety inquiries. + Represents PVRM on post-marketing product… more
    Sumitomo Pharma (08/02/25)
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  • The Head of EGDS Innovation and Center…

    Sanofi Group (Morristown, NJ)
    …such as patient safety/pharmocovigilance, patient focused drug development, portfolio management, global regulatory and digital partners to foster innovation and ... could be critical in helping our teams accelerate progress. We are an innovative global healthcare company with one purpose: to chase the miracles of science to… more
    Sanofi Group (06/05/25)
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  • Vice President, Global Procurement

    Integra LifeSciences (Princeton, NJ)
    …teams to both develop and execute plans. + Deep knowledge of global sourcing, contract manufacturing, and regulatory compliance in medical devices. ... new standards of care. **SUMMARY DESCRIPTION** The Vice President, Global Procurement is a key member of the ...and compliance history. + Collaborate closely with R&D, Quality, Regulatory , Legal, and Operations to ensure alignment across product… more
    Integra LifeSciences (06/19/25)
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  • Director, Supply Chain Enabling

    Western Digital (Trenton, NJ)
    …updates to senior leadership and key stakeholders. + Ensure compliance with global regulatory and sustainability standards throughout the supply chain lifecycle. ... **Company Description** At Western Digital, our vision is to power global innovation and push the boundaries of technology to make what you thought was once… more
    Western Digital (07/23/25)
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  • Vice President Safety Evidence and Sciences

    Bristol Myers Squibb (Princeton, NJ)
    …studies, risk management plans, and signal detection to ensure compliance with global regulatory requirements. **Key Responsibilities** + Oversees a team of ... this team is continually transforming to address new regulation and evolving global data and analytics challenges requiring the development of capabilities to… more
    Bristol Myers Squibb (08/08/25)
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  • Senior Manager, MS&T Mseo Manufacturing Systems…

    Bristol Myers Squibb (Summit, NJ)
    …+ Proven ability to accurately and completely understand, follow, interpret, and apply Global Regulatory and cGMP requirements. + Support health authority and ... in the production and monitoring of personalized cell therapy products for both global clinical trials and commercial supply. The Senior Manager will play a vital… more
    Bristol Myers Squibb (08/08/25)
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  • Senior Director - Clearing and Settlements…

    Broadridge Financial Solutions (Newark, NJ)
    …mechanisms, or settlement agents. + Familiarity with North American or global financial regulatory requirements. + Experience with cloud-native systems ... architecture, network systems and applications infrastructure. + Translate complex regulatory /business requirements into actionable engineering plans; oversee the software… more
    Broadridge Financial Solutions (07/11/25)
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  • Manager, Statistical Programming

    Regeneron Pharmaceuticals (Warren, NJ)
    …advice on complex programming tasks, standards, and processes + Support global regulatory authority submissions including preparing programming result for ... programming project standard to support from the single study through to regulatory approval, product launch, data monitoring boards, regulatory safety reports,… more
    Regeneron Pharmaceuticals (07/31/25)
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  • Medical Director, Clinical Research

    J&J Family of Companies (Raritan, NJ)
    …close partnership with the Compound Development Team (CDTL) and project management, global regulatory affairs, clinical pharmacology, health economics, and the ... the implementation of clinical research studies that are part of a global compound development program. Responsibilities include: + Leads execution of research… more
    J&J Family of Companies (08/01/25)
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