• Assistant Director, Institutional Review Board…

    RWJBarnabas Health (Long Branch, NJ)
    …that all IRB activities and documents are in compliance with OHRP and FDA regulations + Attends local and national conferences and seminars and other ... requested by the Chair and Senior Research Administrator to keep abreast of regulatory and legislative requirements related to research + Facilitate and maintain IRB… more
    RWJBarnabas Health (06/06/25)
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  • Automation Engineer

    Hovione (East Windsor, NJ)
    …and automation of facilities, equipment and utility systems according to regulatory demands (cGMPs, FDA requirements, etc.), industry applicable guidelines ... projects, to meet plans and to deliver the expected quality on time and on budget. - Based on...without compromising the design concept and the process functionality, quality and systems. - Report and escalate promptly any… more
    Hovione (08/08/25)
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  • Senior Director, CNS Communications

    Otsuka America Pharmaceutical Inc. (Princeton, NJ)
    …understanding of important topics including clinical trial design, drug development, regulatory decision making and public policy. + Responsible for comprehensive ... education programs, as well as planning around key data announcements, regulatory milestones and launch planning for late-stage pipeline candidates. + Maintain… more
    Otsuka America Pharmaceutical Inc. (08/14/25)
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  • US Medical Director, RSV Franchise - Vaccines

    Sanofi Group (Morristown, NJ)
    …contribution of medical information and clinical trial data for pharmacovigilance (PV) and regulatory reports to the US FDA and other health authorities + ... Development teams to write, review, edit, and approve key regulatory documents + Engage Key External Leaders (KOLs) to...a wide range of health and wellbeing benefits including high- quality healthcare, prevention and wellness programs and at least… more
    Sanofi Group (08/13/25)
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  • Patient Services Associate

    Penn Medicine (Cherry Hill, NJ)
    …methods as required). + Ensures compliance with all applicable federal, state, and local regulatory standards (ex TJC, DOH, FDA , HIPAA, HCFA, DPW, LCGME, SCGME, ... practice/department in maintaining a patient/customer focus, supports the delivery of high- quality care, shares a passion for patient and customer-centered care, and… more
    Penn Medicine (08/13/25)
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  • Patient Services Associate

    Penn Medicine (Somers Point, NJ)
    …/ Regulatory : . Ensures compliance with all applicable federal, state, and local regulatory standards (ex TJC, DOH, FDA , HIPAA, HCFA, DPW, LCGME, SCGME, etc) ... practice/department in maintaining a patient/customer focus, supports the delivery of high quality care, shares a passion for patient and customer-centered care, and… more
    Penn Medicine (08/09/25)
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  • Sr Tech Support Engineer MI -2

    Fujifilm (Trenton, NJ)
    …of the business, to work on customer systems. + Adheres to the Company's quality and regulatory compliance requirements, without exception, and ensures that all ... + Comply with all applicable US Food and Drug Administration (US FDA ) medical device regulatory requirements, applicable ISO 13485 standard requirements… more
    Fujifilm (08/08/25)
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  • Manager, Industrial Hygiene & Safety

    Bristol Myers Squibb (Summit, NJ)
    …in ensuring workplace safety, employee health protection, and compliance with regulatory standards. The ideal candidate will have comprehensive experience in both ... compounds, and high-containment processes. + Ensure compliance with OSHA, ACGIH, NIOSH, FDA , and other applicable health and safety regulations and guidelines. +… more
    Bristol Myers Squibb (08/08/25)
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  • Patient Services Associate

    Penn Medicine (Atlantic City, NJ)
    …/ Regulatory : + Ensures compliance with all applicable federal, state, and local regulatory standards (ex TJC, DOH, FDA , HIPAA, HCFA, DPW, LCGME, SCGME, etc) ... practice/department in maintaining a patient/customer focus, supports the delivery of high quality care, shares a passion for patient and customer-centered care, and… more
    Penn Medicine (08/07/25)
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  • Senior Director, Communications,…

    Otsuka America Pharmaceutical Inc. (Princeton, NJ)
    …understanding of important topics including clinical trial design, drug development, regulatory decision making and public policy. . Responsible for comprehensive ... education programs, as well as planning around key data announcements, regulatory milestones and launch planning for late-stage pipeline candidates. . Maintain… more
    Otsuka America Pharmaceutical Inc. (07/26/25)
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