• Combination Product Services Site Lead

    BD (Becton, Dickinson and Company) (Branchburg, NJ)
    …ISO) environment + **Technical Skills:** + Strong background in combination product or medical device testing + Knowledge of method development, validation, and ... supporting the success of primary and secondary drug delivery devices . In addition to leading site operations, the Site...regulatory compliance + Deep understanding of drug- device more
    BD (Becton, Dickinson and Company) (08/01/25)
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  • Principal Field Clinical Engineer- North East

    Medtronic (Newark, NJ)
    …**Nice to Have (Preferred Qualifications):** + Experience at Medtronic or within the medical device industry + Experience in the management of clinical ... drive healthcare forward and remain a global leader in medical technology and solutions. To learn more about Inclusion...devices . + Electrophysiology and cardiac ablation device more
    Medtronic (08/22/25)
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  • Associate Engineer, NPD

    J&J Family of Companies (Raritan, NJ)
    …and process controls for manufacturing processes. + Provide technical support for marketed medical device products to other business functions such as ... teams in the design, development, and manufacturing of various devices primarily within wound closure and healing. + Effectively...and regression analysis. + Prior experience working in the Medical Device industry. + Knowledge of … more
    J&J Family of Companies (08/27/25)
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  • Director, SM Medical Affairs, LSM Platform

    BD (Becton, Dickinson and Company) (Franklin Lakes, NJ)
    …experience in clinical investigation + Minimum of 10 years experience in the Medical Device /In Vitro Diagnostics industry required. More than six (6) years ... 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 Purpose,… more
    BD (Becton, Dickinson and Company) (06/18/25)
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  • Clinical Supplier Quality Manager

    J&J Family of Companies (Raritan, NJ)
    …enabling robust GxP Quality Management System of a diverse portfolio of drug and medical device health products and services. This individual serves as the ... to ensure quality of the GxP system, compliance with regulatory requirements and SOPs, and to ensure a continued...field and/or equivalent time and experience in a related medical device R&D area + Good understanding… more
    J&J Family of Companies (08/30/25)
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  • Supervisor, Automated Medical Operations…

    Integra LifeSciences (Plainsboro, NJ)
    …(Collagen Manufacturing Center) to ensure the safety, efficacy, and quality of our medical devices . This includes assigning and monitoring daily 2nd shift ... all established costs, quality, and delivery commitments are met, working within FDA medical device regulations, and applicable ISO standards. + Responsible for… more
    Integra LifeSciences (06/14/25)
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  • Therapeutic Medical Physicist

    Veterans Affairs, Veterans Health Administration (East Orange, NJ)
    …therapy and brachytherapy. The TMP develops, operates and fully documents the medical physics quality assurance program and ensures regulatory compliance within ... therapy, and brachytherapy. The TMP develops, operates and fully documents the medical physics quality assurance program and ensures regulatory compliance within… more
    Veterans Affairs, Veterans Health Administration (08/08/25)
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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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  • Senior Supplier Quality Engineer I - External…

    Integra LifeSciences (Princeton, NJ)
    …Primary responsibilities are to: + Support the development and manufacturing of medical devices in conformance with the Quality System Regulation, ISO ... 13485, Medical Device Directive, ISO 14971, IEC 60601...Engineering or associated scientific discipline. + Minimum 5 years Medical Devices or Pharmaceutical experience in Quality… more
    Integra LifeSciences (07/03/25)
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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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