• Assoc. Dir., Engineering , Combination Products…

    Merck (Rahway, NJ)
    …Reporting into the Director Packaging Platform Technical Leadership the Associate Director Medical Device and Combination Product (MDCP) Platform Packaging and ... ensure compliance with relevant regulations and standards. Ensure thorough engineering, medical device and packaging science is applied to deliverables for… more
    Merck (08/12/25)
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  • Distinguished Scientist, Autoinjector Platform

    Merck (Rahway, NJ)
    …and support of Autoinjectors. The ideal candidate will possess extensive knowledge in medical device engineering, particularly in the design, manufacturing, and ... manufacturing, ensuring robust introduction, qualification, and performance monitoring. + ** Regulatory Compliance ** : + Collaborate closely with...a minimum of 20 years of hands-on experience in medical device engineering, with a focus on… more
    Merck (08/28/25)
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  • Sr Director, Quality & Compliance - Wound…

    J&J Family of Companies (Raritan, NJ)
    …efficiency, advance innovation, enhance organizational capability and diversity, and assure regulatory compliance . In accordance with all applicable federal, ... equivalent experience is preferred. + Experience in a regulated industry ( medical device , biopharmaceutical, or pharmaceutical) + Experience leading… more
    J&J Family of Companies (08/21/25)
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  • Import/Export Compliance Specialist

    Integra LifeSciences (Princeton, NJ)
    …Oracle + Experience in a multi-national manufacturing and distribution organization, medical device or pharmaceutical industry preferred Integra LifeSciences is ... to advance patient outcomes and set new standards of care. The **Import/Export Compliance Specialist** plays a critical role in ensuring full compliance with… more
    Integra LifeSciences (08/21/25)
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  • Director, Combination Product Commercialization

    Merck (Rahway, NJ)
    …in alignment with the company's business goals, and quality and regulatory compliance . **Essential Duties and Responsibilities:** _Strategic Leadership and ... conducted with the highest regard for safety, quality, and regulatory compliance , aligning with the company's divisional...preferred. + Minimum of 10 years of experience in medical device or combination product engineering, with… more
    Merck (08/08/25)
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  • Associate Director, External Manufacturing…

    Merck (Rahway, NJ)
    …and Skills: . **Manufacturing** - Injection Molding and Automated Assembly of Medical Device Components. Final Assembly and Packaging of Combination Products. ... of lean principles, equipment design, and preventative maintenance. . ** Regulatory ** - Global regulations and compliance requirements...development and manufacturing for MDCP (21 CFR Part 4, Medical Device Reporting, ISO 13485:2016, EU … more
    Merck (08/18/25)
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  • Sr. Manager, Indirect Tax

    Terumo Medical Corporation (Somerset, NJ)
    …TMC is part of Tokyo-based Terumo Corporation; one of the world's leading medical device manufacturers with $6+ billion in sales, 30,000+ employees worldwide ... stay updated on the SUT/CAD VAT rules within the medical device industry for multiple jurisdictions. This...in the OneSource Tax Certificate Manager to ensure ongoing compliance with regulatory requirements. + Ensure strict… more
    Terumo Medical Corporation (07/09/25)
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  • Associate Director, Engineering - Packaging…

    Merck (Rahway, NJ)
    …and Qualifications:** + Minimum of 10 years' experience in the pharmaceutical, biotechnology, or medical device industry, with at least 3-5 years in a leadership ... equipment design, development and qualification. + Strong background in the medical device , combination product, pharmaceutical packaging equipment and… more
    Merck (08/29/25)
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  • Director, SM Medical Affairs, LSM Platform

    BD (Becton, Dickinson and Company) (Franklin Lakes, NJ)
    …product ideation, concept development, product verification, and validation, legal and regulatory compliance , demonstration of product value, and stakeholder ... Procedures to optimize MA functioning in terms of leadership, compliance and productivity. The Director, Medical Affairs,...investigation + Minimum of 10 years experience in the Medical Device /In Vitro Diagnostics industry required. More… more
    BD (Becton, Dickinson and Company) (06/18/25)
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  • Staff Quality Engineer II - Post Market…

    BD (Becton, Dickinson and Company) (Franklin Lakes, NJ)
    …professional to join our team in a critical role ensuring product safety and compliance in the medical device industry. **Responsibilities** + **Lead ... and safety **Skills** + ** Regulatory Knowledge:** Extensive understanding of FDA medical device regulations (21 CFR Part 820), ISO standards (13485, 14971),… more
    BD (Becton, Dickinson and Company) (08/27/25)
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