• Oracle Health Physician Executive, Patient Safety…

    Oracle (Harrisburg, PA)
    …. Minimum 7 years' experience in clinical leadership roles within medical device , digital health, or regulated healthcare software sectors. . Extensive experience in ... process, especially for products newly classified under stricter EU medical device rules. . Knowledge of software development processes (including agile and/or… more
    Oracle (12/18/25)
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  • Pennsylvania Clinical Educator

    IQVIA (Philadelphia, PA)
    …patient care responsibilities. You will be at the forefront of cutting-edge medical device technology and gain professional growth and exposure to medical device ... healthcare professionals and advocate for the well-being of patients through medical device technology. Qualified Clinical Educators - will be tasked with educating… more
    IQVIA (12/23/25)
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  • IoT Solutions Specialist - MedTech & Life Sciences

    Cognizant (Harrisburg, PA)
    **Job Title: Solution Sales Specialist - Medical Device R&D | Life Sciences Vertical** **Location:** Bridgewater, NJ **Experience Level:** 14+ Years **Industry:** ... Devices | Product Engineering **Technology Solutions and Sales; Medical Device R&D Engineering** We are seeking a Service Line...Strategic Sales Leader to drive growth in the Medical Device R&D sector within our Life Sciences vertical. This… more
    Cognizant (12/10/25)
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  • Technical Program Manager - BADGE Kiosk Hardware

    Oracle (Harrisburg, PA)
    …and scalable processes. + Serve as the escalation authority for device performance, software/firmware issues, and field incidents. + Author roadmaps, investment ... cases, automation strategies, and device standardization documents. **KEY RESPONSIBILITIES:** + Develop, communicate, and execute the global multi-year strategy and… more
    Oracle (11/25/25)
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  • Technician V - HUP

    Penn Medicine (Philadelphia, PA)
    …Spruce St** **Schedule: Remote** Summary: A Tech V in the remote device clinic remotely monitors patients with cardiac implantable electronic devices (CIEDs) and ... integrates a knowledge base from physiology, pathophysiology, and cardiac device function to perform competent evaluations, diagnostic review, and overall analysis… more
    Penn Medicine (11/13/25)
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  • Senior Quality Manager

    West Pharmaceutical Services (Williamsport, PA)
    …**Work Experience** + 10+ Years of job-related experience required in the Medical Device or Pharmaceutical Industry. + 8+ Years of supervisory experience required. + ... an FDA or ISO regulated industry required, preferably in medical device manufacturing. **Preferred Knowledge, Skills and Abilities** + **Regulatory Skills:**… more
    West Pharmaceutical Services (12/30/25)
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  • Principal TPM, SaMD (Remote)

    Oracle (Harrisburg, PA)
    …and Compliance teams to ensure Oracle's healthcare solutions align with global medical device standards, including **IEC 62304, IEC 82304, ISO 13485, ISO 14971** , ... ensure our software development practices meet the expectations for medical device safety, risk management, usability, security, and post-market surveillance. **Key… more
    Oracle (12/22/25)
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  • Sr. Specialist Regulatory Affairs, MD

    West Pharmaceutical Services (Exton, PA)
    …requests. **Essential Duties and Responsibilities** + Develop and implement medical device regulatory strategies for West's Transfer Devices with an emphasis on ... Bachelor's with 5+ years; Master's degree/PhD with 3+ years of medical device , pharmaceutical or regulatory experience **Work Experience** + Bachelor's with 5+ years… more
    West Pharmaceutical Services (11/14/25)
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  • Sr. Scientist, R&D

    Teleflex (Wyomissing, PA)
    …and validating microbiological and biological test methods for medical device evaluation. This role requires advanced laboratory expertise, strong problem-solving ... findings to leadership and external stakeholders. * Apply knowledge of device usage, complications, and clinical trends (eg, infection, thrombosis, dysfunction) to… more
    Teleflex (12/24/25)
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  • Regulatory Affairs Associate Director, IVD

    GRAIL (Harrisburg, PA)
    …position supports the US Regulatory team in preparing Investigational Device Exemptions (IDEs), IDE supplements, pre-submissions, Premarket Approvals (PMAs), annual ... 510(k)s, post-approval reports, annual reports, export certificates, establishment registrations, and device listings. + Serve as a key member of the Regulatory… more
    GRAIL (12/03/25)
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