• Clinical Educator, Tzield - Pennsylvania - Upstate…

    Sanofi Group (Pittsburgh, PA)
    …role, the TEM will assist patients and caregivers with accessing Sanofi's FDA -approved 14-day T1D infusion therapy. The CE provides disease and product information ... family, with a wide range of health and wellbeing benefits including high- quality healthcare, prevention and wellness programs and at least 14 weeks' gender-neutral… more
    Sanofi Group (08/17/25)
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  • Phlebotomist (Bilingual - English/Spanish)

    CSL Plasma (Temple, PA)
    …donor disconnect. * In compliance with SOPs and Food & Drug Administration ( FDA ) guidelines, performs venipuncture on donors to begin pheresis process. * Evaluates ... necessary corrections in order to expedite donation time and ensure product quality and donor safety. Ensures donation process is efficient and makes adjustments… more
    CSL Plasma (08/16/25)
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  • Patient Delivery Rep, Rx Partners (Casual)

    UPMC (Bridgeville, PA)
    …in timely, safe and accountable manner. + Promote UPMC culture by providing quality , comprehensive services to all customers through a team approach. + Complete ... compliance with State, local, and Federal laws and/or regulations (including FDA , DOT,OSHA,etc.) + Maintain confidentiality of patient information. + Document… more
    UPMC (08/16/25)
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  • Patient Delivery Rep, Rx Partners

    UPMC (Bridgeville, PA)
    …in timely, safe and accountable manner. + Promote UPMC culture by providing quality , comprehensive services to all customers through a team approach. + Complete ... compliance with State, local, and Federal laws and/or regulations (including FDA , DOT,OSHA,etc.) + Maintain confidentiality of patient information. + Document… more
    UPMC (08/16/25)
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  • Production Assistant

    Globus Medical, Inc. (Limerick, PA)
    …and maintaining accurate inventory levels while collaborating with the manufacturing, quality control, and receiving departments. This individual works with all ... + Ensures that all materials are maintained and issued in total conformity with the FDA and other government agencies + Adheres to the letter and spirit of the… more
    Globus Medical, Inc. (08/16/25)
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  • Associate Medical Director, Pharmacovigilance…

    Sumitomo Pharma (Harrisburg, PA)
    …(SmPC), and Canadian Product Monograph (PM) + Ensures timely and quality review and assessment of ICSRs, including seriousness, expectedness, safety narratives, ... and risk management regulations and guidelines, including pre- and post-marketing US FDA and/or EU ICH safety requirements** + Expertise in medical review of… more
    Sumitomo Pharma (08/15/25)
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  • Phlebotomist

    CSL Plasma (Philadelphia, PA)
    …donor disconnect. 2 In compliance with SOPs and Food & Drug Administration ( FDA ) guidelines, performs venipuncture on donors to begin pheresis process. 3 Evaluates ... necessary corrections in order to expedite donation time and ensure product quality and donor safety. Ensures donation process is efficient and makes adjustments… more
    CSL Plasma (08/15/25)
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  • Sales Specialist, Diagnostic Oncology (Central…

    Fujifilm (Harrisburg, PA)
    …and procedures. + Effective communication within FUJIFILM IVD organization of sales, quality and compliance issues. + Utilization of the IVD reporting systems for ... + Comply with all applicable US Food and Drug Administration (US FDA ) medical device regulatory requirements, applicable ISO 13485 standard requirements and all… more
    Fujifilm (08/14/25)
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  • Regional Sales Manager

    ZOLL Medical Corporation (Philadelphia, PA)
    …sleep disorders. Our core product is the WatchPAT(R)️ family, a revolutionary FDA -cleared portable home sleep apnea test device, that is based on proprietary ... patients and provide testing to promote wellness and enhance overall quality of life. WatchPAT(R)️ is commercially available within major markets including… more
    ZOLL Medical Corporation (08/14/25)
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  • Associate Project Engineer - Sustaining

    Globus Medical, Inc. (Audubon, PA)
    …we move with a sense of urgency to deliver innovations that improve the quality of life of patients with musculoskeletal disorders. Our team is inspired by the ... post-market surveillance activities or complaint handling systems. + Understanding of ISO 13485, FDA 21 CFR Part 820, or EU MDR regulations. **Why Join Globus… more
    Globus Medical, Inc. (08/14/25)
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