• Senior Regulatory Affairs Specialist

    Philips (Reedsville, PA)
    …fit if:** + You've acquired 5+ years of experience in the medical device regulatory affairs and/or quality assurance field. Experience authoring SaMD or ... **Senior Regulatory Affairs Specialist (Ultrasound)** The Senior Regulatory...Tech Files required. + Your skills include knowledge of quality system requirements and FDA and/or International product approval… more
    Philips (08/29/25)
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  • Medical Device Regulatory

    Jabil (West Chester, PA)
    …and foster vibrant and diverse communities around the globe. Are you experienced in Medical Device Regulatory Compliance? Jabil is seeking a qualified ... Medical Device Regulatory Compliance Lead to work in...exempt personnel + Knowledge of the US and international medical device quality system regulations,… more
    Jabil (08/29/25)
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  • Associate Manager, Quality Engineering

    Globus Medical, Inc. (Audubon, PA)
    …improvement, or manufacturing operations. + Strong understanding of medical device manufacturing, regulatory compliance, and quality assurance ... Assurance** + Ensure all Globus products and processes meet regulatory and internal quality standards. + Review,...and fast-paced team dedicated to innovation and efficiency in medical device development. + Make a meaningful… more
    Globus Medical, Inc. (06/18/25)
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  • Associate Director, Device Technology

    Merck (West Point, PA)
    …Process, Manufacturing Compliance, Medical Devices, Product Commercialization, Quality Management System Improvement, Regulatory Compliance, Regulatory ... launch in alignment with the company's business goals, and quality and regulatory compliance. **Essential Duties and...Minimum of 8 years of experience in pharmaceutical, biologic, medical device or combination product engineering, with… more
    Merck (08/08/25)
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  • Senior Specialist, Drug/ Device Combination…

    Merck (Harrisburg, PA)
    medical devices and combination products globally. * Experience in design controls, device risk management, medical device , complex combination product ... are the cornerstone of decisions and expectations * Lead technical investigations of medical device and combination product needs for commercial products *… more
    Merck (08/29/25)
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  • Quality Engineer - I ( Medical

    Jabil (West Chester, PA)
    …make an impact? As a Quality Engineer, you will support key quality systems, ensure compliance with internal and regulatory standards, and provide day-to-day ... safety policies and procedures. + Support key business metrics by providing Quality Engineering expertise for manufacturing processes. + Conduct root cause analyses… more
    Jabil (06/27/25)
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  • Device Engineer I

    Teva Pharmaceuticals (West Chester, PA)
    …in Mechanical Engineering, Biomedical Engineering or a related field . 0-2 years Medical Device or Combination Product experience . Strong academic foundation in ... design control practices, physical testing, and documentation to support regulatory filings and product quality . **How you'll...engineering principles and an interest in medical device or drug delivery systems including… more
    Teva Pharmaceuticals (08/09/25)
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  • Medical Device

    Belcan (Pittsburgh, PA)
    Medical Device Job Number: 358762 Category: Regulatory Description: Job Title: Assembler - Medical Device Location: Pittsburgh, PA. Zip Code: 15238 ... JOB RESPONSIBILITIES: This position will assemble and support the various medical device manufacturing processes. POSITION DUTIES & RESPONSIBILITIES: *… more
    Belcan (07/19/25)
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  • Vice President of Regulatory Affairs…

    ZOLL Medical Corporation (Pittsburgh, PA)
    … devices in domestic and international markets. + Post-market surveillance and medical device reporting in domestic and international markets + Responsible ... ZOLL the ideal place to build your career.Job SummaryDirects the activities of the Quality Assurance and Regulatory Affairs department. Ensures the quality more
    ZOLL Medical Corporation (08/08/25)
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  • Regulatory Specialist

    Globus Medical, Inc. (Audubon, PA)
    …or equivalent; Engineering degree is a plus + Minimum of 2-5 years' experience in Regulatory Affairs in the medical device industry, , preferably within ... sense of urgency to deliver innovations that improve the quality of life of patients with musculoskeletal disorders. Our...orthopedic medical devices; + Experience in medical device development and registration of products… more
    Globus Medical, Inc. (06/25/25)
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