• Regional Sales Manager, Cataract Surgical - NJ…

    Bausch + Lomb (Philadelphia, PA)
    …our 170-year history. We have a significant global research, development, manufacturing and commercial footprint of approximately 13,000 employees and a presence ... annual Sales and Revenue plans for assigned Bausch + Lomb Surgical device , equipment and disposable products. This includes managing the day-to-day performance and… more
    Bausch + Lomb (07/25/25)
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  • Field Service Engineer ( 4 years +)

    Medtronic (Abington, PA)
    …robotics or motion control** **Previous experience as Technician/Field Services within medical device industry** **Experience with anatomy, surgical protocol and ... assigned.** **Performing installations, inspections, preventive and corrective maintenance on medical devices and systems.** **Performs a variety of maintenance and… more
    Medtronic (07/15/25)
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  • Dir, Engineering, CMC Leader for Biologics

    Merck (West Point, PA)
    …with our company's Global and regulatory requirements and execute current Good manufacturing Practices (cGMP) in the performance of day-to-day activities and all ... Demonstrated expertise of technical aspects and interdependencies across DS, DP, Device , Packaging, and Analytical, Regulatory, Quality, and Supply Chain from early… more
    Merck (08/08/25)
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  • Senior Specialist, Engineering

    Merck (West Point, PA)
    …test primary and secondary packaging components + Demonstrated understanding of Medical Device and Combination Product regulations + Demonstrated understanding ... areas of Pharmaceutical new product development **Preferred Experience and Skills:** + Medical Device and Combination Product Packaging development experience +… more
    Merck (08/08/25)
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  • Regulatory Compliance Manager

    Jabil (West Chester, PA)
    …preferred. + At least five (5) years of experience in the QSR/ISO-regulated medical device operation, including 2-3 years specific experience in a ... experience, preferably QA exempt personnel + Knowledge of the US and international medical device quality system regulations, standards and best practices (21… more
    Jabil (07/12/25)
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  • Sr. Engineer, R&D, Integrated Systems

    West Pharmaceutical Services (Exton, PA)
    …Engineering preferred **Work Experience** + Minimum 5 years of experience in the medical device or combination products industry + Expertise with test method ... development, validation strategy, and execution + Expertise in medical device design control and change management + Experience in high-volume, automated … more
    West Pharmaceutical Services (07/04/25)
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  • Clinical Production Specialist - 2nd Shift

    Catalent Pharma Solutions (Philadelphia, PA)
    …and seal equipment, card sealing, vial and ampoule labelers, pouch equipment and medical device tray sealing. + Responsible for production involving manual and ... Summary** Catalent, Inc. is a leading global contract development and manufacturing organization (CDMO) whose mission is to develop, manufacture, and supply… more
    Catalent Pharma Solutions (07/22/25)
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  • Global Product Manager, Nutritional Delivery,…

    Cardinal Health (Harrisburg, PA)
    …will also help to support inorganic product opportunities and better define our medical device connectivity strategy. **_Responsibilities_** + Support and be a ... equivalent work experience, preferred. + 4+ years experience in related field, preferred. + Medical device or global medical products experience preferred +… more
    Cardinal Health (07/22/25)
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  • Documentation Technical Writer

    GE HealthCare (State College, PA)
    …procedures across the organization. Qualified candidates will assist with the conversion of medical device history records from a manual/paper platform to a ... College, PA. This position will work closely with the Manufacturing and Engineering teams, as well as other departments...regulated industry and following mandatory processes (preferably in the medical device industry). + Excellent written and… more
    GE HealthCare (07/18/25)
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  • Sr. Specialist, Regulatory Affairs, Product…

    West Pharmaceutical Services (Exton, PA)
    …regulatory/environmental legislations (eg California Prop 65, RoHS, Conflict Minerals, EU Medical Device Regulation) for all West global product portfolios ... Bachelor's with 5+ years required; or + Master's degree/PhD 2+ years medical device regulatory experience required **Preferred Knowledge, Skills and Abilities**… more
    West Pharmaceutical Services (08/09/25)
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