• Associate Director, Regulatory Affairs

    United Therapeutics (Harrisburg, PA)
    …), livers ( **miroliver(R)** ), and a bioengineered external liver assist device for acute liver failure ( **miroliver** **_ELAP_** **(R)** ), with plans ... hearts. **Who you are** We are looking for a regulatory strategist who will advise on regulatory ...in the Company's comprehensive benefits suite of programs, including medical / dental / vision / prescription coverage, employee… more
    United Therapeutics (08/10/25)
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  • Regulatory Specialist A (Abramson Cancer…

    University of Pennsylvania (Philadelphia, PA)
    …trials often include FDA-regulated products, including drugs, medical devices , nutritional products and related materials. Regulatory Affairs Specialists ... health and wellness programs and resources, and much more. Posted Job Title Regulatory Specialist A (Abramson Cancer Center) Job Profile Title Clinical Research … more
    University of Pennsylvania (09/17/25)
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  • Clinical Research Regulatory Affairs…

    University of Pennsylvania (Philadelphia, PA)
    …trials often include FDA-regulated products, including drugs, medical devices , nutritional products and related materials. Regulatory Affairs Specialists ... programs and resources, and much more. Posted Job Title Clinical Research Regulatory Affairs Specialist Job Profile Title Clinical Research Regulatory Specialist… more
    University of Pennsylvania (08/27/25)
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  • Director, Regulatory Policy & Intelligence

    Organon & Co. (Plymouth Meeting, PA)
    **Job Description** **The Position** Leading the Regulatory Policy and Intelligence activities for Global Regulatory Affairs covering all Therapeutic Areas and ... of the world of interest to Organon. **Responsibilities** + Provide Global Regulatory Policy and Intelligence insights to the organization to guide product… more
    Organon & Co. (07/23/25)
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  • Sr. Product Marketing Manager, Kcentra

    CSL Behring (King Of Prussia, PA)
    …experience with 5+ years commercial marketing experience in pharmaceutical, biotech or medical device industry + Preferred experience marketing to HCPs within ... ensuring cost-effective delivery of all programs + Manage the internal legal, regulatory and medical review and approval of new messages and materials to enable… more
    CSL Behring (07/03/25)
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  • Quality Assurance Engineer

    ZOLL Medical Corporation (Pittsburgh, PA)
    …understand the appropriate legal and regulatory requirements in the areas of medical device operations and to establish robust processes and controls to ... that make a meaningful difference in people's lives. Our medical devices , software and related services are...+ Experience in an FDA regulated Class III electrical medical device manufacturing environment preferred.preferred and +… more
    ZOLL Medical Corporation (07/03/25)
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  • Project Coordinator-SDS

    Fujifilm (Harrisburg, PA)
    …+ Comply with all applicable US Food and Drug Administration (US FDA) medical device regulatory requirements, applicable ISO 13485 standard requirements ... and project methodologies to improve efficiency and outcomes. + Quality & Regulatory : Adheres to the Company's quality and regulatory compliance requirements,… more
    Fujifilm (09/11/25)
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  • Sr Clinical Consultant, MI I

    Fujifilm (Harrisburg, PA)
    …II + Comply with all applicable US Food and Drug Administration (US FDA) medical device regulatory requirements, applicable ISO 13485 standard requirements ... and other Key Operators in the use of Fujifilm's Medical Informatics. The Senior Clinical Consultant, MI - I...business activities. + Adheres to the Company's quality and regulatory compliance requirements and ensures that all job duties… more
    Fujifilm (08/11/25)
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  • Biomedical Equipment Technician (I, II & III)

    Penn Medicine (Philadelphia, PA)
    …Responsibilities: + Under close supervision, maintains, repairs, and calibrates patient care medical devices , using general knowledge of lowrisk equipment. + ... sources of replacement materials required to service and maintain medical devices within the facilities. + Maintains...medical hardware, software and equipment products + Understand medical device usage within a health system… more
    Penn Medicine (08/29/25)
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  • Product Support Specialist - MS

    Fujifilm (Harrisburg, PA)
    …+ Comply with all applicable US Food and Drug Administration (US FDA) medical device regulatory requirements, applicable ISO 13485 standard requirements ... **Duties and responsibilities** + Performs hardware and software evaluation of medical imaging systems, components, and accessories to ensure conformance with… more
    Fujifilm (09/11/25)
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