• Sr Staff Scientist - Medical Device

    Astrix Technology (Essex County, NJ)
    …Life Sciences division. This individual will manage initiatives across product development , method validation, risk assessment, and regulatory compliance. **Key ... + Ensure scientific and technical rigor and enforce best practices across all research and development activities. + Develop and refine design input requirements… more
    Astrix Technology (08/11/25)
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  • Director, Cell Banking Leader

    Merck (Rahway, NJ)
    …commercialization. Provide technical oversight of DS & cell banking process development , process characterization and regulatory filing activities to ensure ... control strategies, process comparability reports, Process performance qualification, and/or regulatory submissions. + **CMC RA** : Experience supporting/writing … more
    Merck (10/01/25)
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  • Global Medical Affairs Director - Oncology

    Sanofi Group (Morristown, NJ)
    …scientific communication at Global and Key Market level, preferred. + Broad drug development experience with robust knowledge of regulatory , market access and ... experience, including strong transversal collaboration with key functions such as Research , Clinical Development , Commercial, Health Economics, Value and Access… more
    Sanofi Group (10/02/25)
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  • Medical Director, Global Medical Affairs, Early…

    Otsuka America Pharmaceutical Inc. (Trenton, NJ)
    …- T1) or early development (phase 1) assets either within Medical Affairs, Regulatory Affairs, or Clinical Development is preferred. + Minimum of 7+ years of ... which is comprised of a strong portfolio of individual development and marketed assets. As we continue to develop...and strong competency with the US healthcare system and regulatory landscape is required for this role. + Stay… more
    Otsuka America Pharmaceutical Inc. (07/16/25)
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  • Director, Global Strategic Marketing, Tri-Specific…

    J&J Family of Companies (Raritan, NJ)
    …with key functions across the Global Commercial Strategy Organization (GCSO), J&J Research and Development (R&D), and J&J business regions. **Key ... reports to the Sr. Director, Global Commercial Strategy, Multiple Myeloma Portfolio & Early Development and will be part of the team that leads the development … more
    J&J Family of Companies (09/25/25)
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  • Scientist

    Kelly Services (Skillman, NJ)
    …and other scientists to design experiments and integrate data into broader research and development efforts. + Maintain and operate analytical instruments, ... device The Scientist is tasked with carrying out method development , validation, and interpretation of analytical methods for testing...ensuring compliance with regulatory and safety standards. + Contribute to the preparation… more
    Kelly Services (09/30/25)
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  • Director, Engineering Assembly and Packaging…

    Merck (Rahway, NJ)
    …with internal stakeholders, including packaging commercialization, quality, analytical, regulatory , manufacturing, Device Development and Technology, Technical ... and ensuring the successful completion of projects. This includes the development and execution of robust technical plans across device assembly, packaging,… more
    Merck (08/12/25)
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  • Director Health Tech- Cardiopulmonary

    J&J Family of Companies (New Brunswick, NJ)
    …Function:** Discovery & Pre-Clinical/Clinical Development **Job Sub** **Function:** Clinical Development & Research - MD **Job Category:** People Leader ... that integrates MedTech solutions with pharmaceutical innovation. + Lead the development of implementation plans, milestone tracking, and governance updates across… more
    J&J Family of Companies (09/27/25)
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  • Executive Consultant (VP level)

    Cytel (Trenton, NJ)
    …drug development ), to provide strategic advice to define optimal regulatory , clinical and/or market access pathways and promote faster patient access to ... leader and strategic advisor in the areas of optimal regulatory , clinical development and/or market access pathways...in Mathematics, Biostatistics, or a related field; MBA, MD, PhD or advanced degree highly desirable; at least 15+… more
    Cytel (08/12/25)
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  • Associate Director, Global Medical Oncology, Small…

    Bristol Myers Squibb (Princeton, NJ)
    …Partner closely with medical colleagues in the Markets, with Clinical Research , Regulatory , Commercial, Access, Health Outcomes, MedComms, Competitive ... results in deadline-driven environments. + Deep understanding of global drug development , regulatory processes, and market access dynamics. + Estimated… more
    Bristol Myers Squibb (10/03/25)
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