• 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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  • Associate Director, Medical Affairs…

    BD (Becton, Dickinson and Company) (Franklin Lakes, NJ)
    …work onsite in Franklin Lakes, NJ + At least 3 years of experience in the Medical Device /In Vitro Diagnostics industry. + Minimum 3 years ( _4 preferred_ ) ... 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) (06/29/25)
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  • Director, Packaging Distribution, Components…

    Merck (Rahway, NJ)
    …**Required Skills and Experience:** + Subject matter expertise in packaging and/or medical device and combination product components as well as development ... Performance Indicators (KPI), Leading International Teams, Management Process, Manufacturing Scale-Up, Medical Device Regulations, Medical Devices, Packaging… more
    Merck (08/12/25)
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  • Quality Assurance Engineer II

    Integra LifeSciences (Plainsboro, NJ)
    …13485, the Medical Device Directive, the Canadian Medical Device Regulations (CMDR), and other applicable regulatory agencies. The QA Engineer II ... and guidelines: US Food and Drug Administration (FDA) regulations, ISO 9001, ISO 13485, Medical Device Directive (MOD), the Canadian Medical Device more
    Integra LifeSciences (08/17/25)
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  • Project Manager

    Capgemini (Bridgewater, NJ)
    … management + Strongunderstanding of clinical trial operations, regulatory compliance, anddata privacy. + Excellentcommunication, stakeholder engagement, and ... systems. This includes working closely with cross-functional teams, aligning with regulatory and compliance standards, and ensuring timely delivery of milestones… more
    Capgemini (07/29/25)
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  • Product Manager

    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 ... of 5 years relevant business experience with a minimum of 3 years of medical device marketing, engineering, sales or clinical. + Demonstrated track record of… more
    Terumo Medical Corporation (07/09/25)
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  • Brand Communications Manager

    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 ... media planning and collateral creation. + Ongoing collaboration with medical , regulatory and legal partners to assure...education, training and experience. + Prior experience in the medical device industry and experience in either… more
    Terumo Medical Corporation (07/09/25)
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  • Senior Process Engineer II - Endotoxin

    Integra LifeSciences (Princeton, NJ)
    …Engineer II with a focus on bacterial endotoxin testing programs in the medical device industry. The successful candidate will be responsible for partnering ... a willingness to learn about bacterial endotoxin testing programs, an understanding of medical device quality systems, and a commitment to ensuring product… more
    Integra LifeSciences (07/04/25)
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  • Process Engineer

    Astrix Technology (Somerset County, NJ)
    …+ Added - 19/02/2025 Apply for Job Our client who is a global, Fortune 100 Medical Device company is seeking a Process Engineer to join their team in Somerset ... Process Engineer with 1+ years of experience in the medical device industry. The successful candidate will...and surgical products + Ensure compliance with quality and regulatory standards + Collaborate with R&D, manufacturing, and quality… more
    Astrix Technology (08/20/25)
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  • Supervisor, Product Release

    Integra LifeSciences (Plainsboro, NJ)
    Medical Device Directive, Canadian Medical Device Regulations, and other applicable regulatory agencies/ requirements. **SUPERVISION EXERCISED** ... and evaluates the activities of associates in the Product Release group ,including, Device History Record (DHR) review, final review and release of finished product,… more
    Integra LifeSciences (06/14/25)
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