• Sr. Regulatory Affairs Specialist

    BD (Becton, Dickinson and Company) (Franklin Lakes, NJ)
    …ensure US, EU, and other global regulatory requirements are met. + Evaluates medical device regulations and leads development of global regulatory strategies to ... of all of us-from design and engineering to the manufacturing and marketing of our billions of MedTech products...discipline + 4 years Regulatory Affairs experience in the medical device industry preferred **Preferred Qualifications:** +… more
    BD (Becton, Dickinson and Company) (07/11/25)
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  • Polymer Synthetic Chemist

    Kelly Services (Raritan, NJ)
    **Polymer Chemist** Kelly OCG a Polymer Chemist for our client a leading medical device company in Raritan, NJ. If you're passionate about bringing the latest ... Skills + Demonstrated track record in designing and synthesizing custom polymers for medical device or pharmaceutical use. + Proficient with various polymer… more
    Kelly Services (07/26/25)
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  • Associate Director, Human Factors & Usability…

    Sanofi Group (Morristown, NJ)
    …and documentation This role offers the opportunity to shape the future of medical device usability while working with cutting-edge technology with a global ... flawless planning and meticulous eye for detail of our Manufacturing & Supply teams. With your talent and ambition,...Or related field + Extensive experience in pharmaceutical or medical device industry + Deep knowledge of… more
    Sanofi Group (07/09/25)
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  • Quality Control Inspector I, 2nd Shift

    Integra LifeSciences (Plainsboro, NJ)
    …of overall corporate policies, FDA regulations, ISO 9001, ISO 13485, the medical device directive, and the other applicable regulatory agencies. Expectations ... specific to incoming, line clearance, in-process, and finished goods inspections in pharmaceutical or medical device industry. + QA experience in the medical more
    Integra LifeSciences (08/08/25)
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  • Quality Control Inspector I - 1st shift

    Integra LifeSciences (Plainsboro, NJ)
    …of overall corporate policies, FDA regulations, ISO 9001, ISO 13485, the medical device directive, and the other applicable regulatory agencies. Expectations ... specific to incoming, line clearance, in-process, and finished goods inspections in pharmaceutical or medical device industry. * QA experience in the medical more
    Integra LifeSciences (07/24/25)
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  • Quality Control Inspector I, 2nd Shift

    Integra LifeSciences (Plainsboro, NJ)
    …of overall corporate policies, FDA regulations, ISO 9001, ISO 13485, the medical device directive, and the other applicable regulatory agencies. Expectations ... specific to incoming, line clearance, in-process, and finished goods inspections in pharmaceutical or medical device industry. + QA experience in the medical more
    Integra LifeSciences (06/16/25)
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  • IT System Engineer

    Pentax Medical (Montvale, NJ)
    …Position Opening: Information Technology System Engineer Why JOIN Us? We are an established medical device leader that is preparing for high growth. This means ... CLINICALLY RELEVANT INNOVATION, and SIMPLICITY. Through leading edge R&D and manufacturing , PENTAX Medical provides endoscopic imaging devices and solutions… more
    Pentax Medical (06/28/25)
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  • Senior Facilities Engineer II

    Integra LifeSciences (Plainsboro, NJ)
    …oral and written) both to in-house and external officials, where required. + Medical device critical Facilities experience is preferred. + Demonstrated ability ... a range of facilities critical utilities and equipment projects in the GMP manufacturing , laboratory, support, and non-GMP spaces of the Collagen Manufacturing more
    Integra LifeSciences (07/12/25)
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  • Director Regulatory Affairs

    BD (Becton, Dickinson and Company) (Franklin Lakes, NJ)
    …education and experience. + Preferred minimum of ten-to-fifteen years of experience in the medical device industry, with at least nine years in a regulatory ... of all of us-from design and engineering to the manufacturing and marketing of our billions of MedTech products...legal); and negotiate with Regulators. + Ability to interpret medical device testing methods and statistics, as… more
    BD (Becton, Dickinson and Company) (08/08/25)
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  • Automated Production Operator 2nd Shift

    Integra LifeSciences (Plainsboro, NJ)
    …+ High School Diploma or equivalent with 2+ years of experience in the Medical Device industry or Pharmaceutical industry within a clean room environment ... batch mixing in a new state of the art automated manufacturing environment. Responsibilities include batch execution, in-process quality verifications, equipment… more
    Integra LifeSciences (06/17/25)
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