• Senior Quality Engineer I - Medical

    Integra LifeSciences (Plainsboro, NJ)
    …treatment pathways to advance patient outcomes and set new standards of care. The **Sr.** ** Quality Engineer - Medical Device / Pharma** will provide Plant ... Device Directive, the Canadian Medical Device Regulations (CMDR), and other applicable regulatory ...Experience: 6 to 8 years of experience in a Quality Assurance role for medical device more
    Integra LifeSciences (06/16/25)
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  • Associate Director, Device Technology

    Merck (Rahway, NJ)
    …Manufacturing Compliance, Medical Devices , Product Commercialization, Quality Management System Improvement, Regulatory Compliance, 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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  • 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 ... properly addressed. + Contribute to internal regulatory processes and procedures for medical devices and combination products. + Engage with the relevant … more
    Sanofi Group (07/15/25)
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  • Medical Device , Endoscope…

    Pentax Medical (Montvale, NJ)
    … provides endoscopic imaging devices and solutions to the global medical community. Position Opening: Medical Device , Endoscope Inspection Technician ... role is vital to the production and quality assurance of PENTAX Medical Endoscopes. Responsibilities of Medical Device , Endoscope Inspection Technician:… more
    Pentax Medical (07/14/25)
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  • Device Development Associate Principal…

    Merck (Rahway, NJ)
    …**Job description** This position will be responsible for leading and implementing medical device and combination product design controls for both new ... years of related experience + Has broad knowledge of medical device development, design controls and risk...managed development of DHF (design history file) deliverables for medical devices + Recognized as a subject… more
    Merck (07/31/25)
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  • Distinguished Scientist, Device Tech & Eng…

    Merck (Rahway, NJ)
    …expertise and knowledge of product and process development in the (bio)pharmaceutical and medical device industries to set tactical and strategic direction on ... product launch. The ideal candidate will possess extensive knowledge in medical device engineering, particularly in the design, manufacturing, verification,… more
    Merck (07/29/25)
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  • Director Patient Care Ventricular Assistive…

    RWJBarnabas Health (Newark, NJ)
    …+ Conduct audits and reviews to ensure adherence to CMS guidelines and other regulatory requirements. + Collaborate with quality and compliance teams to address ... Director Patient Care Ventricular Assistive Device (VAD) ProgramReq #:0000189067 Category:Professional / Management Status:Full-Time Shift:Day Facility:Newark Beth… more
    RWJBarnabas Health (06/06/25)
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  • Associate Director, External Manufacturing…

    Merck (Rahway, NJ)
    …that manufacture, assemble, and test complex injection molded Device Components, Device Constituents, and Medical Devices used to deliver Pharmaceutical, ... and Skills: . **Manufacturing** - Injection Molding and Automated Assembly of Medical Device Components. Final Assembly and Packaging of Combination Products.… more
    Merck (05/19/25)
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  • Quality Engineer ( Medical

    Astrix Technology (Rahway, NJ)
    ** Quality Engineer ( Medical Devices )** Engineering Rahway, NJ, NONE + Added - 08/08/2025 Apply for Job + **Schedule** : Onsite ~8a-5p M-F + **Salary** : ... technology solutions for some of the worlds most complex medical devices . **ESSENTIAL DUTIES AND RESPONSIBILITIES:** +...and standards. + Anager in the maintenance of the quality management system in compliance with appropriate regulatory more
    Astrix Technology (08/09/25)
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  • 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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