• Research Coordinator - Heart Vascular Research…

    WellSpan Health (York, PA)
    …and some evenings **General Summary** Coordinates clinical research activities and compliance to study requirements, and patient and staff considerations relative to ... collection of research data for patients in clinical trials. Assists the medical investigators in achieving the objectives of clinical research studies and supports… more
    WellSpan Health (07/22/25)
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  • Java Developer

    Robert Half Technology (Philadelphia, PA)
    …to the development and enhancement of a multi-tenant platform for device and network service lifecycle management. This platform automates network operations ... Implement API data validation routines within CRUD interfaces to ensure schema compliance . + Create proprietary search/query APIs to support web-based automation of… more
    Robert Half Technology (08/22/25)
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  • Clinical Systems Analyst (Associate, Mid, or Sr.)

    Penn Medicine (Philadelphia, PA)
    …leaders in the field of medicine. Working for this leading academic medical center means collaboration with top clinical, technical and business professionals across ... you living your life's work? Entity: Corporate Services Department: IS - Medical Decision Support Location: 3535 Market Street, Philadelphia, PA (The role involves… more
    Penn Medicine (08/07/25)
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  • Associate Director External Quality Assurance

    Organon & Co. (Plymouth Meeting, PA)
    …of global GMP Quality Systems and regulatory requirements. + Experience in medical device Quality Systems is preferred, including familiarity with ISO13485, ... complexity of in-markets, regulatory history, historical performance (production and compliance ), new product or market launches, historical relationship between… more
    Organon & Co. (08/19/25)
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  • Quality & Commissioning Manager

    NTT America, Inc. (Harrisburg, PA)
    …where you can grow, belong and thrive. **KEY RESPONSIBILITIES** + Ensures work compliance within Federal, State, and local guidelines as well as requirements related ... + Reviews equipment submittals and shop drawings for overall compliance with the design intent. + Reviews final pre-functional...with working remotely and use of a personal mobile device , if applicable. NTT Global Data Centers Americas, Inc.… more
    NTT America, Inc. (07/16/25)
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  • Regional Business Manager - Pittsburgh

    Takeda Pharmaceuticals (PA)
    …+ Bachelors' degree - BA/BS + Minimum of 5 + years of pharmaceutical or medical device sales and/or relevant clinical or industry experience + Ability to discuss ... in a manner that is truthful and non-misleading, consistent with Takeda compliance policies and all applicable laws and regulations. + Individual must manage… more
    Takeda Pharmaceuticals (08/28/25)
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  • Virology Customer Representative - St. Louis, MO

    Merck (Harrisburg, PA)
    …with a preference for launch experience. + Experience in pharma, biotech or medical device sales. + Demonstrated experience developing and executing plans for ... the highest standards of ethics and integrity, with particular emphasis on compliance with all relevant laws, policies and regulation. **Virology Specific:** The… more
    Merck (08/26/25)
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  • Procurement 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 ... but not limited to Sick, Jury Duty, Bereavement, Personal, and Parental Leave + Medical , Dental, and Vision Insurance Benefits effective DAY ONE + 401K - with… more
    Envista Holdings Corporation (08/08/25)
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  • Sr Clinical Consultant, MI I

    Fujifilm (Harrisburg, PA)
    …+ Comply with all applicable US Food and Drug Administration (US FDA) medical device regulatory requirements, applicable ISO 13485 standard requirements and all ... and other Key Operators in the use of Fujifilm's Medical Informatics. The Senior Clinical Consultant, MI - I...changes to improve efficiency and customer satisfaction. + Ensure compliance with all applicable requirements of the company's quality… more
    Fujifilm (08/11/25)
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  • Principal, Quality Assurance, GMP

    West Pharmaceutical Services (Exton, PA)
    …8 years of quality-related experience with preferred experience in pharmaceutical and/or medical device industry + Expertise of cGMP requirements, ISO standards ... **Job Summary** The Principal, Quality Assurance, GMP role focuses on ensuring compliance with cGMP standards within the WSS laboratories by identifying gaps,… more
    West Pharmaceutical Services (08/24/25)
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