• Quality Engineer

    GE HealthCare (State College, PA)
    …quality. + Collaborate with cross-functional teams, including R&D, production, and regulatory affairs , to support product development and production transfer ... other teams and contributes to the area. GE HealthCare is a leading global medical technology and digital solutions innovator. Our mission is to improve lives in the… more
    GE HealthCare (06/10/25)
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  • Radiation Therapist - (Radiation Oncology)…

    UPMC (Harrisburg, PA)
    …Assists at other UPMC Radiation Oncology locations if the need arises. + Regulatory Affairs Management: Participates in regulatory compliance activities and ... patient education/side effect management information and indicates non-compliance to medical /nursing staff. Maintains a safe, orderly treatment room. Under the… more
    UPMC (06/07/25)
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  • Clinical Research Coordinator (Department…

    University of Pennsylvania (Philadelphia, PA)
    …lab. + Assist the Research Project Manager in submitting documents to regulatory authorities (eg IRB, FDA, etc.) and/or review/monitoring boards (ie, DSMB, ... to protocol. Includes maintenance of study source documents and essential regulatory documents; reporting of adverse events; understanding of good clinical practice… more
    University of Pennsylvania (05/23/25)
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  • Senior Actuary - Medicare Part D

    CVS Health (Blue Bell, PA)
    …process development related to pricing and bid development activities, regulatory compliance, competitive analysis, and risk-revenue analysis. The colleague will: ... with business partners to analyze the impact of proposed legislative or regulatory reform and implement required changes in pricing activities. + Collaborate with… more
    CVS Health (05/16/25)
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  • Research Specialist C (Department of Cancer…

    University of Pennsylvania (Philadelphia, PA)
    …Dr. Li have earned publication authorship and successfully transitioned to graduate/ medical schools and industry positions. Successful candidates will have a strong ... of equipment and reagents) and develop protocols for research and regulatory compliance (eg animal protocols, bio-safety protocols, etc.). + Contribute to… more
    University of Pennsylvania (05/04/25)
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  • Clinical Research Coordinator

    University of Pennsylvania (Philadelphia, PA)
    …website with materials and articles for patients. + Submit documents to regulatory authorities (eg IRB, FDA, etc.) and/or review/monitoring boards (ie, DSMB, ... to protocol. Includes maintenance of study source documents and essential regulatory documents; reporting of adverse events; understanding of good clinical practice… more
    University of Pennsylvania (05/04/25)
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  • Director, HCP Marketing - Orgovyx

    Sumitomo Pharma (Harrisburg, PA)
    …and peer-to-peer education. + Collaborate cross-functionally with Sales, Sales Training, Medical Affairs , Market Access, Omnichannel, Patient Marketing, Legal, ... salary increases, short incentive plan participation, eligibility for our 401(k) plan, medical , dental, vision, life and disability insurances and leaves provided in… more
    Sumitomo Pharma (05/01/25)
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  • Enrollment Analyst - Office of the University…

    University of Pennsylvania (Philadelphia, PA)
    …(NSLDS). The Analyst is responsible for ensuring institutional compliance with regulatory enrollment reporting requirements and upholding the integrity of student ... Suite, Freshservice, and other enterprise tools used in academic records and regulatory functions is preferred. + Demonstrated aptitude for quickly mastering new… more
    University of Pennsylvania (06/12/25)
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  • Clinical Research Coordinator A/B

    University of Pennsylvania (Philadelphia, PA)
    …Summary The Clinical Research Coordinator is responsible for oversight, execution, and regulatory compliance of human subject research carried out in the Stroke ... including patient recruitment, data collection and management, and potentially some regulatory responsibilities. The coordinator must be detail oriented and have… more
    University of Pennsylvania (06/10/25)
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  • Senior Product Software Engineer - Quality…

    Capgemini (Pittsburgh, PA)
    …where applicable. + Assist with complaint investigation and documentation interfaces with Regulatory Affairs to support UL, IEC, and FDA submissions. ... Participates in internal audits conducted by internal employees and regulatory agencies. + Develop and execute supplier qualification processes,...a related field. + 8 years of experience in medical device quality engineering or a related field. +… more
    Capgemini (06/09/25)
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