• Associate Director, Government Contracts

    Bristol Myers Squibb (Princeton, NJ)
    …in their personal lives. Read more: careers.bms.com/working-with-us . **Summary:** The Associate Director of Government Contracts will become a subject matter expert ... impact government gross-to-nets. + Interpret changing CMS guidance and new regulatory proposals as they are released. Quantify potential impact, adjust projection… more
    Bristol Myers Squibb (08/10/25)
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  • Associate Director, Government Pricing

    Bristol Myers Squibb (Princeton, NJ)
    …work and in their personal lives. Read more: careers.bms.com/working-with-us . **Summary:** The Associate Director of Government Pricing is a key leader in the US ... ongoing compliance with external and internal requirements and guidance including regulatory , SOX and audit. + Evaluate new and modified contracting proposals,… more
    Bristol Myers Squibb (08/08/25)
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  • Associate Actuary

    AIG (Parsippany, NJ)
    …are reimagining the way we help customers to manage risk. Join us as a Associate Actuary Analyst to play your part in that transformation. It's an opportunity to ... at a pricing segment level. + Monitor loss trends, relevant industry, and regulatory changes and effectively communicate to management impacts on business. + Review… more
    AIG (08/02/25)
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  • Associate Director, Program Management

    Organon & Co. (Jersey City, NJ)
    …improve the lives of women globally. We are looking for an experienced Associate Director, Program Management to join our team. This successful candidate will ... Education, Experience and Skills** + Bachelor's degree in a scientific, life science , technical discipline, or relevant field. + Five years of industry experience​… more
    Organon & Co. (07/23/25)
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  • Associate , Data Analytics

    SMBC (Jersey City, NJ)
    …and Analytics, in the Compliance Department, Americas Division, the Data Analytics Associate performs detailed analytics work in an independent fashion in support of ... to develop and test tools and systems in line with policy and regulatory expectations. + Collect, aggregate, and analyze e-communications data to identify trends and… more
    SMBC (07/08/25)
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  • Associate Director, Promotional Materials

    Taiho Oncology (Princeton, NJ)
    …collaborators and partners, and each other. Together, we are working on cutting-edge science and growing our portfolio and pipeline across a range of tumor types ... promotional and medical materials review committees. Position Summary: ​​ The Associate Director, Promotional Materials will provide guidance to the Promotional… more
    Taiho Oncology (07/04/25)
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  • Associate Control Systems Engineer Nuclear

    PSEG (Salem County, NJ)
    …as the attention, camaraderie, and care for one another you might typically associate with a small business. Our focus on combatting climate change through clean ... walkdowns, installation, testing and as-built verification. * Comply with regulatory requirements including 50.59, License Amendment Request preparation and any… more
    PSEG (06/24/25)
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  • Associate Director, Marketing

    Merck (Rahway, NJ)
    …our focus is on innovation and launch execution excellence; we translate breakthrough science into innovative medicines that help people around the globe. We are ... currently recruiting for Associate Director, US Marketing The role will oversee foundational...align on decisions, including field sales, marketing operations, Legal, Regulatory , Medical, etc. Our US marketing team has adopted… more
    Merck (06/08/25)
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  • Associate Director, Translational Medicine…

    Bristol Myers Squibb (Princeton, NJ)
    …expertise in disease biology, neuroinflammation and patient segments to assist science driven strategies for the development of the neuroscience pipeline. **Position ... Diseases. + Manage relationships with key internal stakeholders including regulatory , clinical and commercial and scientific communications and external… more
    Bristol Myers Squibb (08/10/25)
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  • Associate Director Quality Assurance…

    BeOne Medicines (Pennington, NJ)
    …and vendor qualification. + Development of all necessary SOPs, ensuring regulatory compliance in conjunction with being appropriate both clinical and commercial ... or adverse events requiring documented review and action. + Participation in regulatory and customer inspections/audits. + Subject matter expert in GMPs: 21 CFR… more
    BeOne Medicines (08/08/25)
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