• Sr Tech Support Engineer MI -2

    Fujifilm (Trenton, NJ)
    …+ Comply with all applicable US Food and Drug Administration (US FDA) medical device regulatory requirements, applicable ISO 13485 standard requirements ... to work on customer systems. + Adheres to the Company's quality and regulatory compliance requirements, without exception, and ensures that all job duties… more
    Fujifilm (08/08/25)
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  • Lead, Clinical Data Management - MedTech

    J&J Family of Companies (Raritan, NJ)
    …. + At least 6+ years of clinical data management experience in Medical Device or Pharmaceuticals including experience of successful active participation in ... execution including timelines milestones and budgets. + Lead efforts co-ordinating with Medical Affairs organization to facilitate data coding and safety reviews as… more
    J&J Family of Companies (08/29/25)
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  • Document/Change Management Specialist

    Kelly Services (Mahwah, NJ)
    …management systems preferred. + Basic knowledge and understanding of US and International Medical Device Regulations. + Ability to plan, organize, and implement ... document related changes in accordance with change management procedures and relevant regulatory requirements for medical devices. This role will be a… more
    Kelly Services (08/13/25)
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  • Sales Specialist, Diagnostic Oncology (Central…

    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 (08/14/25)
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  • Sr Director, Trade and Distribution

    Mitsubishi Chemical Group (Jersey City, NJ)
    …of product distribution: DME, Orals, and Solutions + Firm grasp of legal, regulatory and compliance issues in the healthcare space + Analytical/strategic thinker ... respected - is a research-driven pharmaceutical company that has tirelessly pursued medical breakthroughs with global reach. MTPC has discovered and produced several… more
    Mitsubishi Chemical Group (07/15/25)
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  • 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 ... for project and or post go-live support cases in compliance with the company's quality procedures. **Company Overview** At...+ Ability to work effectively with customers in the medical field. + Ability to prioritize and handle multiple… more
    Fujifilm (06/19/25)
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  • Resident Sales Distribution Manager

    System One (Jersey City, NJ)
    …field. + Minimum 5+ years of experience in sales and distribution management ( medical device , pharmaceutical, or related field preferred). + Proven track record ... + Prepare weekly sales forecasts, reports, and performance analyses. + Ensure compliance with regulatory requirements, ethical standards, and company quality… more
    System One (08/27/25)
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  • Associate Paralegal

    NTT America, Inc. (Trenton, NJ)
    …related to construction and energy projects. + Support legal team in regulatory filings, permitting processes, and compliance tracking. + Maintain organized ... experience with: + FERC, OSHA, EPA, or other relevant regulatory bodies. + supporting renewable energy or infrastructure projects....with working remotely and use of a personal mobile device , if applicable. NTT Global Data Centers Americas, Inc.… more
    NTT America, Inc. (08/29/25)
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  • Equipment and Controls Technician

    Kinder Morgan (Hewitt, NJ)
    …report, and correct safety and environmental concerns. Perform all work in compliance with Company standards, procedures, and regulatory and tariff requirements. ... nights and weekends. Kinder Morgan offers a robust benefits package including medical , dental, vision, life insurance, two retirement plans, paid holidays, paid time… more
    Kinder Morgan (07/25/25)
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  • Supervisor, Production - Weekend (Friday - Sunday)

    Integra LifeSciences (Plainsboro, NJ)
    …all established costs, quality, and delivery commitments are met, working within FDA medical device regulations, and applicable ISO standards. + Responsible for ... to ensure minimum costs, prevent operational delays, and maintain quality and regulatory compliance standards. + Trains and ensures all assigned employees… more
    Integra LifeSciences (07/08/25)
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