• Vice President, Head US Supply Chain

    Teva Pharmaceuticals (Parsippany, NJ)
    …+ High customer service levels (CSL) and strong internal stakeholder alignment + Compliance with all regulatory and quality standards + Effective risk management ... Company: Teva Pharmaceuticals Job Id: 63487 **Who We Are:** Teva is a global pharmaceutical leader and the world's largest generic medicines producer, committed to… more
    Teva Pharmaceuticals (08/12/25)
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  • Clinical Development Program Lead, Neuropsychiatry…

    Bristol Myers Squibb (Madison, NJ)
    …success filing regulatory dossiers and prosecuting them through approval + Global experiences is a plus since this position has responsibility for strategy and ... Clinical Development Program Leader sits within Clinical Development, which is a global organization dedicated to the effective design and execution of drug… more
    Bristol Myers Squibb (08/30/25)
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  • Principal Medical Writer Associate Director

    Sanofi Group (Morristown, NJ)
    …Our mission is to synergize and harness evolving technologies pushing the edge of regulatory writing. We are an innovative global healthcare company with one ... to get started? **Main Responsibilities:** **Document Development** + Create high-quality regulatory -compliant clinical documents supporting product life cycle +… more
    Sanofi Group (08/28/25)
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  • Assistant General Counsel, Specialty Care

    Sanofi Group (Morristown, NJ)
    …all Oncology product related commercial matters. . Sit on the Global & US Oncology Leadership Teams, delivering proactive engagement, impact and enterprise ... the company's strategic goals while effectively managing legal and regulatory risks and upholding the company's integrity and reputation....Global & US Oncology. + Provide input into product launch planning and advise on brand and commercial… more
    Sanofi Group (08/14/25)
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  • Summer Intern, Research & Development Quality

    Bristol Myers Squibb (Princeton, NJ)
    …of audit programs by observing and participating in audits to assess regulatory compliance . + Use data analytics to generate business-relevant reports. ... Regulatory Affairs, and Medical Affairs activities throughout the product lifecycle. Conducting audits of processes, affiliate operations, and third parties… more
    Bristol Myers Squibb (09/05/25)
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  • Assoc. Dir, HVAC

    Merck (Rahway, NJ)
    …Plant Maintenance, Preventative Maintenance Programs, Process Control Systems, Project Management, Regulatory Compliance , Regulatory Requirements {+ 3 more} ... NJ Site. + Develop, implement, and maintain HVAC operational strategies that ensure compliance with GxP (as applicable) and other regulatory requirements. + Lead… more
    Merck (08/29/25)
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  • Digital Program Manager

    Sanofi Group (Morristown, NJ)
    …risk management, compliance , and associated mitigations. We are an innovative global healthcare company with one purpose: to chase the miracles of science to ... search deeper and solve sooner than ever before. The Global Program leader is accountable to deliver large ...user experience. + Is responsible for the delivery quality, compliance with regulatory (Data Privacy, GxP, SOX,… more
    Sanofi Group (08/08/25)
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  • Strategic Planning Sr Director

    ADP (Roseland, NJ)
    …and expand cross-functional (internal and external) business partnerships including Sales, Finance, Global Product & Technology, Compliance Solutions, Legal ... beneficial relationships that will accelerate growth. + Anticipates business and regulatory issues; recommends product , process or service improvements. +… more
    ADP (07/25/25)
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  • Sr. Manager, Indirect Tax

    Terumo Medical Corporation (Somerset, NJ)
    …exemption certificates in the OneSource Tax Certificate Manager to ensure ongoing compliance with regulatory requirements. + Ensure strict adherence to policies, ... This individual will establish corporate-wide policies and procedures to ensure compliance with multiple US, Canadian, and Puerto Rican jurisdictions for TAH… more
    Terumo Medical Corporation (07/09/25)
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  • Sr Staff Scientist - Medical Device

    Astrix Technology (Essex County, NJ)
    …initiatives across product development, method validation, risk assessment, and regulatory compliance . **Key Responsibilities:** + Lead the design and ... This high-impact, visible role is key to driving innovation, product improvements, and global expansion within the...of technical documentation to support regulatory submissions, global market entry, and ongoing compliance . +… more
    Astrix Technology (08/11/25)
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