• Implementation Project Manager

    ManpowerGroup (Phillipsburg, NJ)
    …on track. **What's Needed?** + Bachelor's degree in business, Project Management, Scientific or Engineering discipline. + Minimum of five (5) years of experience ... deliverables. + Strong background in GMP regulations, ISO9000, and regulatory affairs . + Excellent prioritization, organization, and problem-solving skills. If this… more
    ManpowerGroup (09/10/25)
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  • Global Brand Lead Tzield (HCP Activation - EI…

    Sanofi Group (Morristown, NJ)
    …+ 10+ years across critical functions including Market Access, HEOR, Medical, External Affairs or similar relevant experience + The ability to collaborate with a ... With more than 100,000 people in 100 countries, Sanofi is transforming scientific innovation into healthcare solutions around the globe. Discover more about us… more
    Sanofi Group (09/04/25)
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  • Sr. Manager, Sales Operations & Analytics

    Taiho Oncology (Princeton, NJ)
    …strong relationships with internal partners (Marketing, Sales, Market Research, Medical Affairs , etc.) collaborating effectively to ensure team success. + Create ... create unique business insights. + Ability to read, analyze and interpret scientific and technical information and data. + Excellent communication & presentation… more
    Taiho Oncology (09/03/25)
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  • Associate Director, Regulatory Policy

    Bristol Myers Squibb (Princeton, NJ)
    …team, the Associate Director Regulatory Policy brings an expertise in regulatory affairs and related policy. The Associate Director, Regulatory Policy is responsible ... departments. **Responsibilities include, but are not limited to:** + **Identify Emerging Scientific and Regulatory Trends** : assess their impact on the company's… more
    Bristol Myers Squibb (08/30/25)
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  • Associate Director, Small Molecule Analytical…

    Otsuka America Pharmaceutical Inc. (Trenton, NJ)
    … affairs , quality assurance, and other departments to drive scientific excellence, resolve complex technical issues, and ensure compliance with applicable ... regulations and guidelines. + Provide CMC functional representation on wider cross-functional program development teams, ensuring all CMC considerations are accounted for in wider clinical development plans. + Serve as early-stage CMC representative of the… more
    Otsuka America Pharmaceutical Inc. (08/27/25)
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  • Regional CPE Director, Tzield…

    Sanofi Group (Jersey City, NJ)
    …CPE Directors, Account Directors, Regional Business Directors, Medical, PSS, Medical Affairs , HEOR, Marketing, and all other departments necessary to facilitate ... With more than 100,000 people in 100 countries, Sanofi is transforming scientific innovation into healthcare solutions around the globe. Discover more about us… more
    Sanofi Group (08/20/25)
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  • Lead Intellectual Property Counsel

    Dr. Reddy's Laboratories (Princeton, NJ)
    …extensive interaction with Portfolio, R&D, Business Development, and Regulatory Affairs . **Responsibilities:** + Manage patent litigations in North America, ... guiding principle behind all our actions. We see healthcare solutions not only as scientific formulations, but as a means to help patients lead healthier lives, and… more
    Dr. Reddy's Laboratories (08/08/25)
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  • Head of Privacy, SpeCare and North America

    Sanofi Group (Morristown, NJ)
    …+ You will co-author internal position papers with Legal and Government Affairs , representing Sanofi in industry advocacy efforts with Trade associations, and Data ... With more than 100,000 people in 100 countries, Sanofi is transforming scientific innovation into healthcare solutions around the globe. Discover more about us… more
    Sanofi Group (07/18/25)
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