• Principal Regulatory Technical Documentation…

    Oracle (Harrisburg, PA)
    …Oracle Health Data Intelligence is entering a high-impact phase of **MDR ( Medical Device Regulation)** readiness and **regulatory transformation** . Over the ... (Regulatory / Health Tech)** + Experience with one or more of: + MDR ( Medical Device Regulation) + ISO 14971 (risk management) + ISO 13485 + IEC 62304 +… more
    Oracle (12/20/25)
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  • Principal Technical Program Manager - Health…

    Oracle (Harrisburg, PA)
    …role will help ensure **operational alignment with international compliance frameworks and medical device regulatory requirements** as HDI scales its solutions ... Certification:** Collaborate with legal, regulatory, and product stakeholders to support ** medical device certification and compliance activities** as HDI… more
    Oracle (12/20/25)
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  • Healthcare Ethics and Compliance Operations…

    Oracle (Harrisburg, PA)
    …programs, policies, training and monitoring. + Experience with Software as a Medical Device marketing and promotion compliance requirements. + Experience with ... and development of the company, + Track evolving healthcare and medical device industry standards and codes, risk identification and mitigation strategies, in… more
    Oracle (11/25/25)
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  • Principal Regional Field Educator

    Medtronic (PA)
    …or sales/service/engineering in the Cardiac Ablation, Cardiac Rhythm, or Implantable Medical Device Industry OR + Advanced Degree in Engineering ... sales/service/engineering in the Cardiac Ablation, Cardiac Rhythm, or Implantable Medical Device Industry **Desired/Preferred qualifications:** + IBHRE/RCES… more
    Medtronic (01/03/26)
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  • MedTech Part Time Clinical Nurse Consultant -North

    IQVIA (Philadelphia, PA)
    …an understanding of their applications. + Improve patient outcomes by delivering ventricular medical device education in a variety of settings, including but not ... limited to, the ICU, OR, and Cath Lab. + Ventricular medical device case support, including on call support. + Complete proactive rounds for patients receiving… more
    IQVIA (12/20/25)
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  • Electrical Engineer (Hybrid-Quakertown, PA)

    Envista Holdings Corporation (Quakertown, PA)
    …operations, regulatory and quality backgrounds that work collaboratively in the fast-paced medical device field. A friendly and open atmosphere helps to ... 10%, as needed. **PREFERRED QUALIFICATIONS:** + MS degree preferred. + Medical device design and compliance experience. + Compliance Engineering: + Performed GAP… more
    Envista Holdings Corporation (12/06/25)
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  • QA Specialist

    Envista Holdings Corporation (Quakertown, PA)
    …operations, regulatory and quality backgrounds that work collaboratively in the fast-paced medical device field. A friendly and open atmosphere helps to ... equivalent plus 3 years of experience working in a quality assurance, medical device and/or manufacturing setting or associate degree in relevant field such as… more
    Envista Holdings Corporation (11/26/25)
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  • Field Service Engineer 1

    BD (Becton, Dickinson and Company) (Harrisburg, PA)
    …and service department procedures and policies, including customer complaint handling and Medical Device Reporting + Able to work independently and also ... OS, network experience, required + CompTIA A+ Certification, required + Medical device or electromechanical device service/repair experience, required +… more
    BD (Becton, Dickinson and Company) (12/17/25)
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  • Technician Manufacturing (Cleanroom Packaging) 1st…

    dsm-firmenich (Exton, PA)
    …biomaterial science and process innovation, and the leading resource for global medical device and pharmaceutical companies. **Your key responsibilities** + ... experience in related fields. + 0-5 years' experience, preferably in Medical Device manufacturing or GMP related industry. + Packaging experience, preferably in… more
    dsm-firmenich (11/25/25)
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  • Principal Regulatory Affairs Specialist

    Philips (New Kensington, PA)
    …design changes, and field safety corrections, with a primary focus on Software as a Medical Device (SaMD) for our Sleep & Respiratory Care products in the US, ... a minimum of 7+ years' experience in Regulatory Affairs/Strategy within FDA regulated Medical Device environments. + You have proven expertise in Software as… more
    Philips (11/11/25)
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