• Principal Software Engineer - Cloud

    Otsuka America Pharmaceutical Inc. (Harrisburg, PA)
    …expertise in applying FDA design control requirements (21 CFR ) as applied to medical device software and medical device regulation (IEC-62304) ... developers in the delivery of products, both in an R&D and Commercial setting + Estimate engineering effort, plan...CI/CD for AWS serverless deployments + PHI/PII and/or Med device or other device -related experience + Demonstrated… more
    Otsuka America Pharmaceutical Inc. (08/08/25)
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  • Sr Prod Mgr Interv GI & Access

    Fujifilm (Harrisburg, PA)
    …manager, senior product manager, product/technical director). + Minimum 8 years of medical device experience with strong clinical background. + Prior experience ... R&D , operations, regulatory, global marketing, infection control, other companies/ device manufacturers, etc.) + Build and maintain strong relationships with Key… more
    Fujifilm (08/11/25)
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  • Vice President of Research and Development

    ZOLL Medical Corporation (Pittsburgh, PA)
    …of complex electronic and software systems required. + Experience with medical device development including regulatory requirements required. Knowledge, Skills ... innovative technologies that make a meaningful difference in people's lives. Our medical devices, software and related services are used worldwide to diagnose and… more
    ZOLL Medical Corporation (07/14/25)
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  • Spring TDS Proteins API Ceas Automation Co-Op

    J&J Family of Companies (Spring House, PA)
    …testing through the development process across all sectors including Pharmaceutical, Medical Device , Consumer and Corporate/Enterprise. We offer a fast-paced ... in Spring house, PA. **Research & Development Co-op Overview:** J&J R&D encompasses the development of sophisticated materials, process improvements, risk management… more
    J&J Family of Companies (09/26/25)
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  • Medical Director, Interventional Urology…

    Teleflex (Wayne, PA)
    …in compliance with FDA's Quality System Regulation (QSR), ISO13485, the Canadian Medical Device Regulations, and all other international regulatory requirements ... Medical Director, Interventional Urology and Urology Care (REMOTE)...scientific aspects of IUBU-sponsored clinical studies. * Partner with R&D and Marketing within the IUBU to contribute substantively… more
    Teleflex (07/08/25)
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  • Supplier Quality Engineer

    Philips (Murrysville, PA)
    …years' experience in Supplier Quality Engineering within highly regulated product environments ( Medical Device preferred), with a focus on supplier selection, ... SPC, SCAR's, SICR, CAPA, Remediation etc. + You have detailed knowledge of medical device regulations, requirements, and standards, such as 21 CFR Parts… more
    Philips (09/26/25)
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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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  • Sr Technical Program Manager - Medical

    Capgemini (Pittsburgh, PA)
    …proven experience in technologies like AWS, Java, Spring Boot, Python, Angular, device connectivity, Linux, and cybersecurity in a highly regulated industry like ... and communication skills. + Experience in the full software life cycle in the medical domain is a plus \#LI-JE1 **Life at Capgemini** Capgemini supports all aspects… more
    Capgemini (08/09/25)
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  • Sr. Project Manager ( Medical Devices, NPI…

    Philips (New Kensington, PA)
    …Minimum of 8+ years of professional experience in product/solution development within FDA-regulated medical device or technology sectors. + Minimum of 8+ years ... ensuring alignment with strategic business objectives. + Coordinate with Quality, Regulatory, R&D , Operations, and Marketing teams to meet goals related to quality,… more
    Philips (08/14/25)
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  • Senior Specialist, Supplier Quality

    West Pharmaceutical Services (Exton, PA)
    …5 years of quality related experience with preferred experience in pharmaceutical and/or medical device industry + Experience working with suppliers and supplier ... process is preferred + Knowledge of cGMP, cGDP, relevant ISO standards, medical device requirements and other international regulations + Familiarity with… more
    West Pharmaceutical Services (09/26/25)
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