• Associate Director, Government Pricing

    Bristol Myers Squibb (Princeton, NJ)
    …as appropriate. + Participate on cross-functional teams as a subject matter expert representing the Government Pricing team as required to evaluate and implement ... special projects. + Assist and lead team with implementation of system & process improvements as appropriate with internal and external business partners + Drive… more
    Bristol Myers Squibb (08/22/25)
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  • Customer Experience Analytics and Innovation Lead…

    Sanofi Group (Morristown, NJ)
    …times, and support team performance, using this information to recommend process improvements + Leaddeep-dive analyses to identify operational bottlenecks, ... process inefficiencies, and opportunities for improvement in the customer...enhance the customer experience + Act as subject matter expert and leader for all customer experience innovation initiatives… more
    Sanofi Group (08/17/25)
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  • Principal Scientist - Biologics Potency, Cell…

    Merck (Rahway, NJ)
    …assays. More specifically, the ideal candidate will be a recognized expert developing mechanism-of-action reflective potency assays for the development of ... minimum of 14 years of relevant experience in the pharmaceutical industry. + Expertise in applying advanced cell biology...for interpretation of potency data in context of broader process and product development. + Working knowledge of regulatory… more
    Merck (08/16/25)
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  • Associate Director, Device Technology

    Merck (Rahway, NJ)
    …drug delivery systems. The associate director will be a technical subject matter expert on the device components and combination products and lead a cross functional ... (Master's or PhD) preferred. + Minimum of 8 years of experience in pharmaceutical , biologic, medical device or combination product engineering, with at least 4 years… more
    Merck (08/08/25)
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  • Sr MES PAS-X Specialist role

    Capgemini (Raritan, NJ)
    …metrics, and for communication between the GMP operations teams and the process development scientific groups. This position will be focused on performing PAS-X ... with external programs (SAP, PI, and DeltaV) Experience of working in pharmaceutical industry and knowledge of GxP regulations will be preferred Provide day-to-day… more
    Capgemini (07/26/25)
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  • Technical Writer Compliance

    Actalent (Parsippany, NJ)
    …Writer Compliance Job Description We are seeking a Technical Writer Compliance expert to manage and complete investigations and deviations from a compliance and ... to prevent recurrence. + Manage multiple investigations in different stages of the process to meet compliance deadlines and product release dates. + Collaborate with… more
    Actalent (09/04/25)
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  • Sr. Manager, Sales Operations & Analytics

    Taiho Oncology (Princeton, NJ)
    …Manage the auto-reimbursement program (Motus) + Manage the credentialing vendors and credentialing process + Manage field roster + Must work and thrive in a ... years quantitative analytical or forecasting experience. + 2+ years pharmaceutical analytics / sales / managed markets experience. +...insights to larger issues. Sought out as an analytical expert and, more importantly, as a strategic adviser. +… more
    Taiho Oncology (09/03/25)
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  • Lead Patient Support Specialist - Afford Svcs

    PSKW LLC dba ConnectiveRx LLC (Whippany, NJ)
    …journey, pharmaceutical manufacturers rely on us to untangle the process and create a clear path-allowing patients to build trusting relationships with ... committed to taking the pain out of the prescription process , but we're also devoted to bringing the brightest...with daily responsibilities by acting as the subject matter expert . Keeps track of the team's progress to help… more
    PSKW LLC dba ConnectiveRx LLC (08/29/25)
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  • Associate Director, Congress Engagement

    Bristol Myers Squibb (Princeton, NJ)
    …role positions the Congress Excellence Team as a subject matter expert -ensuring alignment with organizational goals and enhancing the overall congress experience ... and execution in all phases of the congress to drive continuous process improvement. + Design and implement innovative approaches to enhance customer experience… more
    Bristol Myers Squibb (08/29/25)
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  • Associate Director, Commercial Regulatory Affairs-…

    Bristol Myers Squibb (Princeton, NJ)
    …Commercial Regulatory Affairs requires the ability to apply complex scientific and expert regulatory advice and risk assessment for the development of promotional ... and advertising will be based + Provide input on process improvement and BMS guiding principles as needed +...Regulatory promotional review or related 5 to 8 years pharmaceutical experience (eg, Medical promotional review) + Experience providing… more
    Bristol Myers Squibb (08/25/25)
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