• Regional Director, Modality Solutions (West Coast)

    Fujifilm (Trenton, NJ)
    …Other + Comply with all applicable US Food and Drug Administration (US FDA ) medical device regulatory requirements, applicable ISO 13485 standard requirements ... sales team for Digital Radiography and CT products. **Company Overview** At FUJIFILM Healthcare Americas Corporation, we're on a mission to innovate for a healthier… more
    Fujifilm (06/04/25)
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  • Principal Engineer - Systems

    Lilly (Branchburg, NJ)
    …to make life better for people around the world. We are a global healthcare leader headquartered in Indianapolis, Indiana. Our employees around the world work to ... and supports laboratory and/or manufacturing systems to meet business and regulatory needs. This position requires business area knowledge and computer expertise… more
    Lilly (08/02/25)
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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 ... adhering to all safety policies and procedures. **Company Overview** At FUJIFILM Healthcare Americas Corporation, we're on a mission to innovate for a healthier… more
    Fujifilm (08/16/25)
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  • Account Executive, ES (Western PA/Western VA…

    Fujifilm (Trenton, NJ)
    …+ Comply with all applicable US Food and Drug Administration (US FDA ) medical device regulatory requirements, applicable ISO 13485 standard requirements ... achieving a 10% annual increase of market share. **Company Overview** At FUJIFILM Healthcare Americas Corporation, we're on a mission to innovate for a healthier… more
    Fujifilm (08/15/25)
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  • ENDOSCOPY Clinical Specialist or Advanced GI…

    Fujifilm (Trenton, NJ)
    …+ Comply with all applicable US Food and Drug Administration (US FDA ) medical device regulatory requirements, applicable ISO 13485 standard requirements ... resource for the Company and its sales team. **Company Overview** At FUJIFILM Healthcare Americas Corporation, we're on a mission to innovate for a healthier world,… more
    Fujifilm (08/09/25)
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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 ... adhering to all safety policies and procedures. **Company Overview** At FUJIFILM Healthcare Americas Corporation, we're on a mission to innovate for a healthier… more
    Fujifilm (08/08/25)
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  • Specialist, Clinical Apps - MRI

    Fujifilm (Trenton, NJ)
    …+ Comply with all applicable US Food and Drug Administration (US FDA ) medical device regulatory requirements, applicable ISO 13485 standard requirements ... operation of Fujifilm Magnetic Resonance Imaging Products. **Company Overview** At FUJIFILM Healthcare Americas Corporation, we're on a mission to innovate for a… more
    Fujifilm (07/02/25)
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  • Technician, Installation (Mechanical)

    Fujifilm (Trenton, NJ)
    …+ Comply with all applicable US Food and Drug Administration (US FDA ) medical device regulatory requirements, applicable ISO 13485 standard requirements ... new/existing super-conductive MRI systems at customer sites. **Company Overview** At FUJIFILM Healthcare Americas Corporation, we're on a mission to innovate for a… more
    Fujifilm (06/01/25)
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  • Pharmacovigilance Audit and Inspection Readiness…

    Sanofi Group (Morristown, NJ)
    …Audit and Inspection Readiness team as an Expert. We are an innovative global healthcare company with one purpose: to chase the miracles of science to improve ... Safety and Pharmacovigilance (PSPV) and country PV offices in anticipation of regulatory inspections and audits. + Active involvement in the preparation, conduct,… more
    Sanofi Group (08/27/25)
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  • Senior Clinical Research Director, I&I

    Sanofi Group (Bridgewater, NJ)
    **About the Job** We are an innovative global healthcare company with one purpose: to chase the miracles of science to improve people's lives. We're also a company ... submission dossier for their projects: Common Technical Document for FDA & EMA submission, filing in Japan and China...for research projects + Represents his/her project at key regulatory agency meetings as the medical spokesperson for the… more
    Sanofi Group (07/06/25)
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