• Senior Technical Clinical Consultant (PACS,…

    Fujifilm (Trenton, NJ)
    …+ Comply with all applicable US Food and Drug Administration (US FDA) medical device regulatory requirements, applicable ISO 13485 standard requirements ... and or post go-live support cases in compliance with the company's quality procedures. **Company Overview** At FUJIFILM Healthcare Americas Corporation, we're on a… more
    Fujifilm (06/19/25)
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  • Clinical Engineering Supervisor

    Agiliti Health (Paterson, NJ)
    … equipment management experts who proudly serve hospitals and healthcare facilities to ensure quality medical equipment is in the right place at the right time ... repairs, preventive maintenance and calibration. + Participate in hazard identification and medical device reporting procedures. + Instruct customer personnel on… more
    Agiliti Health (05/29/25)
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  • Head of Privacy, SpeCare and North America

    Sanofi Group (Morristown, NJ)
    …or PhD in LifeScience; Law or Computer Sciences + **Pharmaceutical, biotech, medical device industry experience required** + Demonstrated experience in working ... to generate deeper insights to our Research, Marketing, commercial and medical activities. + Actively monitor North American privacy regulations/enforcements, and… more
    Sanofi Group (07/18/25)
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  • Endoscopic Repair Technician

    Fujifilm (Wayne, NJ)
    …+ Comply with all applicable US Food and Drug Administration (US FDA) medical device regulatory requirements, applicable ISO 13485 standard requirements ... **Position Overview** This position is responsible for technical repair and final quality inspection on assigned Endoscopic units. This position is responsible for… more
    Fujifilm (08/08/25)
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  • Marketing Manager, US Product Marketing SM

    BD (Becton, Dickinson and Company) (Franklin Lakes, NJ)
    …the time **Preferred Qualifications:** + Digital Marketing experience. + Experience in the Medical device industry. + SalesForce experience At BD, we prioritize ... Description** We are **the makers of possible** BD is one of the largest global medical technology companies in the world. Advancing the world of health (TM) is our… more
    BD (Becton, Dickinson and Company) (06/18/25)
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  • Clean Room Manufacturing Operator

    Integra LifeSciences (Plainsboro, NJ)
    …+ 0 - 2 years of chemical processing experience or batch mixing in Medical Device or Pharmaceutical manufacturing industry. Production experience in a clean room ... records, required logs, books, and other procedures to comply with regulatory requirements, Good Manufacturing Practices (GMP), Quality Systems Regulations,… more
    Integra LifeSciences (07/22/25)
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  • Manufacturing Operator 1- 2nd Shift

    Integra LifeSciences (Plainsboro, NJ)
    …0 - 2 years of chemical processing experience or batch mixing in Medical Device or Pharmaceutical manufacturing industry. Production experience is highly ... required logs, books, records, and other procedures to comply with regulatory requirements, Good Manufacturing Practices (GMP), Quality Systems Regulations,… more
    Integra LifeSciences (06/17/25)
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  • Associate Scientist

    Sokol Materials & Services (Skillman, NJ)
    …full suite of GxP services tailored to the pharmaceutical, biotechnology, cell therapy, and medical device industries. Our mission is to help clients achieve ... regulatory compliance while upholding the highest standards of product quality and safety. Our customized solutions are designed to guide clients through complex … more
    Sokol Materials & Services (08/13/25)
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  • Sr. Program Manager

    BD (Becton, Dickinson and Company) (Franklin Lakes, NJ)
    …devices/products. + Minimum of 5-8 years project management experience. + Experience in medical device industries required, including experience in FDA or other ... of possible** BD is one of the largest global medical technology companies in the world. Advancing the world...design and development process is followed, ensuring compliance with quality management systems and regulatory requirements, where… more
    BD (Becton, Dickinson and Company) (07/26/25)
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  • Sales Specialist, Diagnostic Oncology (West Coast)

    Fujifilm (Trenton, NJ)
    …+ Comply with all applicable US Food and Drug Administration (US FDA) medical device regulatory requirements, applicable ISO 13485 standard requirements ... with Key Accounts and Opinion Leaders within the Liver/Hepatology Medical Oncology community. Manage specific assigned geographic areas and successfully… more
    Fujifilm (08/03/25)
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