• Medical Device Regulatory

    Oracle (Trenton, NJ)
    …driving Oracle's success and competitiveness in the healthcare and life sciences sector. As a Medical Device Regulatory Affairs Strategist, you will work ... with SaMD in areas such as Regulatory Affairs , Quality Compliance, Product Development, etc. in medical... Affairs , Quality Compliance, Product Development, etc. in medical device industry or equivalent. Experience authoring… more
    Oracle (12/22/25)
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  • Sr. Regulatory Affairs Specialist

    Cardinal Health (Trenton, NJ)
    …in related field or equivalent work experience, preferred + 2+ years' experience in Medical Device Regulatory Affairs /Quality experience preferred + ... **_What Regulatory Affairs contributes to Cardinal Health_**... and product development consulting services to enable pharmaceutical, medical and biotechnology companies to obtain regulatory more
    Cardinal Health (12/13/25)
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  • Regulatory Affairs Associate…

    GRAIL (Trenton, NJ)
    …, development, clinical affairs , quality, or program management within the IVD, medical device , or pharmaceutical industries is required. + Regulatory ... FDA and/or global health authorities. + Support the US Regulatory Affairs team in preparing submissions such...and international regulatory frameworks and processes for medical device development and approvals is required.… more
    GRAIL (12/03/25)
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  • Senior Manager, CMC Global Regulatory

    Otsuka America Pharmaceutical Inc. (Trenton, NJ)
    **Job Summary** The Chemistry, Manufacturing and Controls (CMC) Global Regulatory Affairs (GRA) professional is responsible for developing and executing global ... relationships with other local and/or global functional units [OPC CMC Global Regulatory Affairs , Global Regulatory Strategy, Manufacturing facilities,… more
    Otsuka America Pharmaceutical Inc. (12/02/25)
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  • Director, Early Precision Medicine…

    Bristol Myers Squibb (Princeton, NJ)
    …more: careers.bms.com/working-with-us . **Position Summary** The Director of Early Precision Medicine Regulatory Affairs leads global regulatory strategy for ... Solid scientific background, PhD., MD, PharmD, MS + Significant experience in regulatory affairs and diagnostic-related development eg, >8-10 years. + Scientific… more
    Bristol Myers Squibb (12/03/25)
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  • Sr. Manager, Regulatory Affairs Cell…

    ThermoFisher Scientific (Cranbury, NJ)
    …or helping find cures for cancer. **Discover Impactful Work** As a Sr. Manager, Regulatory Affairs , you will play a crucial role in interpreting and ... requirements and desired marketing claims. + Author and/or review regulatory submissions, specifically device master files, ...count on, which includes: + A choice of national medical and dental plans, and a national vision plan,… more
    ThermoFisher Scientific (11/08/25)
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  • Senior Counsel ( Medical Device )

    Fujifilm (Trenton, NJ)
    …**Job Description** **Responsibilities** + Manage and support the day-to-day legal affairs of assigned Medical Device businesses or ... Counsel and senior business management on general legal and regulatory risks affecting the Medical Device businesses, including with respect to healthcare… more
    Fujifilm (12/16/25)
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  • Associate Director, Regulatory Intelligence

    Otsuka America Pharmaceutical Inc. (Trenton, NJ)
    …development programs. + Build professional network with key stakeholders outside of Global Regulatory Affairs to identify regulatory intelligence needs and ... in a scientific or technical discipline preferred. + Minimum of 5 years of regulatory affairs experience. + Minimum 2-3 years' work experience in regulatory more
    Otsuka America Pharmaceutical Inc. (11/13/25)
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  • Senior Director, Clinical Leader - Neuropsychiatry

    J&J Family of Companies (Titusville, NJ)
    …publications emerging from the Team and its affiliates + Assists Regulatory Affairs in the development of drug/ device regulatory strategies and ... interactions also includes individuals from project management, TA strategy, global regulatory affairs , finance, legal, quality assurance, quality monitoring &… more
    J&J Family of Companies (12/06/25)
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  • Lead SaMD Technical Program Manager

    Wolters Kluwer (Princeton, NJ)
    …a pivotal role in driving the development and delivery of Software as a Medical Device (SaMD) products. This position is responsible for enabling engineering ... The Principal SaMD TPM acts as a bridge between engineering, product, regulatory affairs , clinical, and quality assurance teams, facilitating strategic… more
    Wolters Kluwer (12/04/25)
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  • Sr. Professional and Clinical Trainer

    Terumo Medical Corporation (Somerset, NJ)
    …TMC is part of Tokyo-based Terumo Corporation; one of the world's leading medical device manufacturers with $6+ billion in sales, 30,000+ employees worldwide ... and Clinical Training Managers, Sales, Field clinical, Marketing, and Medical Affairs to ensure training curriculum and...3 years of relevant sales training experience in a medical device or pharmaceutical environment or equivalent… more
    Terumo Medical Corporation (10/02/25)
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  • Sr. Clinical Quality Specialist

    Terumo Medical Corporation (Somerset, NJ)
    …TMC is part of Tokyo-based Terumo Corporation; one of the world's leading medical device manufacturers with $6+ billion in sales, 30,000+ employees worldwide ... Date: Dec 18, 2025 Req ID: 5279 Location: Somerset, NJ, US Company: Terumo Medical Corporation Department: Clinical Affairs Terumo Medical Corporation (TMC)… more
    Terumo Medical Corporation (10/22/25)
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  • Senior Director, CDTL - Neuropsychiatry

    J&J Family of Companies (Titusville, NJ)
    …and Device Development and Regulation, Program Management, Regulatory Affairs Management, Relationship Building, Safety-Oriented, Scientific Research, ... via matrix interactions includes individuals from TA strategy, GCSO, global regulatory affairs , project management, finance, legal, quality assurance, quality… more
    J&J Family of Companies (12/06/25)
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  • Medical Education Program Specialist

    Philips (Mercerville, NJ)
    ** Medical Education Program Specialist** You will be responsible for the development, facilitation, execution, documentation, and monitoring of our customer-facing ... Structural Heart Disease (SHD) medical training and educational programs as part of a...forecasting, while maintaining vendor relationships and financial compliance. Uphold regulatory standards and audit readiness for all educational activities,… more
    Philips (12/13/25)
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  • Electrical Engineer (Hybrid-Quakertown, PA)

    Envista Holdings Corporation (Quakertown, PA)
    regulatory and quality backgrounds that work collaboratively in the fast-paced medical device field. A friendly and open atmosphere helps to foster ... Up to 10%, as needed. **PREFERRED QUALIFICATIONS:** + MS degree preferred. + Medical device design and compliance experience. + Compliance Engineering: +… more
    Envista Holdings Corporation (12/06/25)
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  • Manager, Global Product Quality - Controlled…

    Otsuka America Pharmaceutical Inc. (Trenton, NJ)
    …Minimum 5 - 7 years of experience in a regulated industry (pharmaceutical or medical device ), with 3-5 years in pharmaceutical quality, with specific experience ... TrackWise, or similar. + Certification in DEA compliance, Quality Assurance, or Regulatory Affairs . **Disclaimer** This job description is intended to describe… more
    Otsuka America Pharmaceutical Inc. (12/16/25)
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  • Manager, Clinical Research Monitoring

    Edwards Lifesciences (Trenton, NJ)
    …patients in need. In close partnership with principal investigators, dedicated medical professionals, patient advocacy groups, and regulatory authorities, you ... and how our products transform patients' lives. As part of our Clinical Affairs team, you'll hone your scientific curiosity and passion for evaluating data to… more
    Edwards Lifesciences (12/18/25)
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  • VP, Deputy General Counsel, International

    Integra LifeSciences (Princeton, NJ)
    …intercompany loans ; + Providing product counseling and guidance on commercial and regulatory affairs initiatives to ensure compliance with applicable laws and ... with substantial experience supporting international business activities. Pharmaceutical or medical device industry experience preferred; + Comfort navigating… more
    Integra LifeSciences (10/30/25)
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  • Manager, Professional Education- Cleveland…

    J&J Family of Companies (Raritan, NJ)
    …/ customer knowledge along with exceptional collaboration and teamwork with Faculty, Medical Affairs , Marketing, Sales, Strategic Accounts and MedTech. The ... is responsible for adhering to all applicable legal and regulatory requirements as well as Company Health Care Compliance...years of experience in the healthcare industry, preferably in medical device . + 3 years of experience… more
    J&J Family of Companies (12/04/25)
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