• Staff Regulatory Affairs Specialist

    BD (Becton, Dickinson and Company) (Franklin Lakes, NJ)
    …technical discipline required (eg, engineering, bioengineering, biology, chemistry). + Minimum 5 years Regulatory Affairs experience in medical device or in ... has the unique opportunity to be involved with both medical devices and in vitro diagnostics, allowing...regulatory authority personnel (eg FDA, Notified Bodies) in medical device and in vitro diagnostic areas.… more
    BD (Becton, Dickinson and Company) (07/18/25)
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  • Sr. Regulatory Affairs Specialist

    BD (Becton, Dickinson and Company) (Franklin Lakes, NJ)
    …US, EU, and other global regulatory requirements are met. + Evaluates medical device regulations and leads development of global regulatory strategies ... Specialist independently supports projects to bring new and modified medical devices to market and ensure ongoing...4 years Regulatory Affairs experience in the medical device industry preferred **Preferred Qualifications:** +… more
    BD (Becton, Dickinson and Company) (07/11/25)
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  • Regulatory Affairs Specialist-Ad Promo

    Kelly Services (Bridgewater, NJ)
    ** Regulatory Specialist - Ad Promo ( medical device )** Kelly(R) Science & Clinical is seeking a Regulatory Specialist for our client, a leading medical ... experience in a regulated environment. 5+ years of ad/promo experience relevant to medical devices . + Strong organizational skills and excellent in managing… more
    Kelly Services (08/08/25)
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  • Director, US Regulatory Affairs…

    Sanofi Group (Morristown, NJ)
    …responsibilities. **About You** **Experience:** + 8+ years of experience within pharmaceutical or medical device Regulatory Affairs + Successful track record ... **Job Title:** Director, US Regulatory Affairs - Advertising and Promotion **Location:** Cambridge,...+ Dealt effectively with cross-functional groups, which may include Medical , Legal, Marketing, etc. + Experience managing others is… more
    Sanofi Group (08/08/25)
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  • Senior Counsel ( Medical Device )

    Fujifilm (Trenton, NJ)
    …to Division General Counsel and senior business management on general legal and regulatory risks affecting the Medical Device businesses, including with ... part of the legal team providing support to the Medical Device businesses of FUJIFILM Healthcare Americas...The Senior Counsel, reporting to the Division General Counsel, Medical Devices , will be an experienced commercial… more
    Fujifilm (08/08/25)
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  • GRA Device Lead (Director)

    Sanofi Group (Morristown, NJ)
    …(early phase, late stage and marketed products). + Develop innovative and sustainable medical device regulatory strategies covering combination products and ... to internal regulatory processes and procedures for medical devices and combination products. + Engage...regulatory experience. At least 5 years of relevant medical device and/or combination product regulatory more
    Sanofi Group (07/15/25)
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  • Associate Director, Device Technology

    Merck (Rahway, NJ)
    …Moldings, Management Process, Manufacturing Compliance, Medical Devices , Product Commercialization, Quality Management System Improvement, Regulatory ... managing external partners in the scale-up, development, commercialization, and transfer of medical devices and combination products, with a focus on… more
    Merck (08/08/25)
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  • Senior Specialist, Drug/ Device Combination…

    Merck (Rahway, NJ)
    …& Technology Team, with responsibilities supporting the commercialization and sustainment of medical devices and combination products globally. * Experience in ... design controls, device risk management, medical device ,...experience to develop value-add solutions to customer needs in medical devices and combination products * Secure… more
    Merck (08/29/25)
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  • Sr Staff Scientist - Medical Device

    Astrix Technology (Essex County, NJ)
    **Sr Staff Scientist - Medical Device ** Science & Research Essex County, NJ, US Pay Rate Low: 128000 | Pay Rate High: 184000 + Added - 27/05/2025 Apply for Job ... _Our client, a world-leading medical device company focused on improving lives...Minimum of 10 years' relevant industry experience, ideally within medical devices , pharmaceuticals, or biotechnology. + Direct… more
    Astrix Technology (08/11/25)
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  • Senior Quality Engineer I - Medical

    Integra LifeSciences (Plainsboro, NJ)
    Medical Device Directive, the Canadian Medical Device Regulations (CMDR), and other applicable regulatory agencies. **Primary responsibilities are:** ... patient outcomes and set new standards of care. The **Sr.** **Quality Engineer - Medical Device / Pharma** will provide Plant Quality compliance support for the… more
    Integra LifeSciences (06/16/25)
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