• Associate Director, Drug/ Device

    Merck (Rahway, NJ)
    …Materials Engineering, or similar **Experience** **8+ years of experience in medical device or combination product engineering.** **Demonstrated technical ... leadership in Technology Transfer and Design Transfer for medical device and combination product component manufacturing, assembly, and packaging, with specific… more
    Merck (08/16/25)
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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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  • 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...initiatives across product development, method validation, risk assessment, and regulatory compliance. **Key Responsibilities:** + Lead the design and… more
    Astrix Technology (08/11/25)
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  • Director Patient Care Ventricular Assistive…

    RWJBarnabas Health (Newark, NJ)
    Director Patient Care Ventricular Assistive Device (VAD) ProgramReq #:0000189067 Category:Professional / Management Status:Full-Time Shift:Day Facility:Newark Beth ... Israel Medical Center Department:Cardiac Recovery Room Pay Range:$125,000.00 - $175,000.00...NJ 07112-2027 Job Title: Director Patient Care Ventricular Assistive Device (VAD) Program Location: Newark Beth Israel Med Ctr… more
    RWJBarnabas Health (06/06/25)
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  • Associate Director External Quality Assurance

    Organon & Co. (Jersey City, NJ)
    …global GMP Quality Systems and regulatory requirements. + Experience in medical device Quality Systems is preferred, including familiarity with ISO13485, ... and distributed in accordance with Organon expectations and all applicable regulatory requirements. The External Systems Quality Leader (ESQL) serves a leadership… more
    Organon & Co. (08/19/25)
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  • IT Sales -Managed Services/Life Sciences-Med-…

    NTT DATA North America (Newark, NJ)
    …apply now. We are currently seeking a IT Sales -Managed Services/Life Sciences-Med- Device (Remote) to join our team in Newark, New Jersey (US-NJ), United ... services, and industry vertical solutions to include things like regulatory compliance solutions, digital solutions, mobile solutions, transformational services and… more
    NTT DATA North America (07/04/25)
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  • Assoc Endoscopic Repair Tech

    Fujifilm (Wayne, NJ)
    …+ Comply with all applicable US Food and Drug Administration (US FDA) medical device regulatory requirements, applicable ISO 13485 standard requirements ... preferred, but will consider applicants with repair experience in electronics, medical device , mechanical, or a similar field. + Soldering experience preferred.… more
    Fujifilm (08/16/25)
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  • Business Development Mgr, ESD (East Coast)

    Fujifilm (Trenton, NJ)
    …+ Comply with all applicable US Food and Drug Administration (US FDA) medical device regulatory requirements, applicable ISO 13485 standard requirements ... of experience with a Master's degree. + Minimum 8 years of medical device industry experience in a clinical capacity (clinical demonstration and education) with… more
    Fujifilm (07/24/25)
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  • Sr Clinical Consultant, MI I

    Fujifilm (Trenton, NJ)
    …II + Comply with all applicable US Food and Drug Administration (US FDA) medical device regulatory requirements, applicable ISO 13485 standard requirements ... and other Key Operators in the use of Fujifilm's Medical Informatics. The Senior Clinical Consultant, MI - I...business activities. + Adheres to the Company's quality and regulatory compliance requirements and ensures that all job duties… more
    Fujifilm (08/11/25)
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  • Lead Project Engineer

    Fujifilm (Trenton, NJ)
    …+ Comply with all applicable US Food and Drug Administration (US FDA) medical device regulatory requirements, applicable ISO 13485 standard requirements ... go-live.. Lead PE's must have expert level knowledge in all areas of medical informatics, IT infrastructure design and deployment, medical imaging industry in… more
    Fujifilm (08/13/25)
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