• Technical Publications Specialist

    Stryker (Mahwah, NJ)
    …the Technical Publications Specialist, you will play a key role in ensuring our medical device labeling is clear, compliant, and accessible, supporting safe and ... in labeling or documentation within a regulated industry + Familiarity with compliance standards and regulatory requirements **$** **58,700** - **$98,000**… more
    Stryker (08/15/25)
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  • Pharmaceutical Quality Engineer

    Kelly Services (Somerset, NJ)
    …support within a regulated industry (pharmaceutical, biotech, or medical device ). + Experience with system validation and compliance documentation ... for the position. + Adhere to company standards for data integrity and regulatory compliance . **Education and Experience:** + Bachelor's degree in engineering,… more
    Kelly Services (08/14/25)
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  • CQV Engineer Mid-Level

    Sokol Materials & Services (Skillman, NJ)
    …experience in CQV and/or CSV within the pharmaceutical, biotechnology, cell therapy or medical device industries. + Experience with Cell Therapy equipment (cell ... including plans, test protocols, summary reports, and traceability matrices, ensuring regulatory compliance and accuracy. * Investigate and resolve deviations… more
    Sokol Materials & Services (07/24/25)
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  • VP, Quality Systems, Innovative Medicine (USA)

    J&J Family of Companies (New Brunswick, NJ)
    …Systems and/or Operations Management in a highly regulated industry (Pharmaceutical, Medical Device or similarly regulated industry) **Required Knowledge, Skills ... performance management. This role focuses on aligning quality systems with regulatory requirements and organizational objectives while fostering a culture of… more
    J&J Family of Companies (08/22/25)
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  • CQV Engineer Senior Level

    Sokol Materials & Services (Skillman, NJ)
    …Minimum of 7 years of CQV experience in pharmaceutical, biotechnology, cell therapy, or medical device industries, with at least 5 years focused on utilities and ... protocols, summary reports, and traceability matrices, ensuring technical accuracy and compliance with regulatory requirements. * Investigate and resolve… more
    Sokol Materials & Services (06/24/25)
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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 ... but will consider applicants with repair experience in electronics, medical device , mechanical, or a similar field....held religious belief or other legally required exemption._ _In compliance with the ADA Amendments Act, should you have… more
    Fujifilm (08/16/25)
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  • Quality Associate

    Actalent (Basking Ridge, NJ)
    …with internal procedures. The role involves coordinating labeling projects to ensure regulatory compliance and providing guidance to team members on labeling ... files according to internal procedures. + Coordinate labeling projects to ensure regulatory compliance . + Provide guidance on labeling regulations and process… more
    Actalent (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 ... with a Master's degree. + Minimum 8 years of medical device industry experience in a clinical...held religious belief or other legally required exemption._ _In compliance with the ADA Amendments Act, should you have… more
    Fujifilm (07/24/25)
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  • Sr. MES Opcenter OR Camstar Consultant - Remote

    Cognizant (Trenton, NJ)
    …cross-functional teams developing, and supporting information systems in the Medical Device and pharmaceutical manufacturing industries Understand the ... deep understanding of business processes under GxP, ISO, and regulatory compliance Knowledge of Mfg. Process Controls...of Electronic Lot History Records using Camstar Software for Medical Device / Pharma industries Implement and execute… more
    Cognizant (07/18/25)
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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 ... of Privacy Officers. You will be part of Sanofi Privacy Leadership and US Compliance Leadership team We are an innovative global healthcare company with one purpose:… more
    Sanofi Group (07/18/25)
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