• Senior Director, Communications,…

    Otsuka America Pharmaceutical Inc. (Princeton, NJ)
    …as a general understanding of important topics including clinical trial design, drug development, regulatory decision making and public policy. . Responsible ... 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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  • Clinical Research Nurse

    Actalent (Hackensack, NJ)
    …Nurse (OCN). Additional Skills & Qualifications + BSN preferred. + Knowledge of FDA regulatory , IND reporting, and proficiency in Microsoft or similar Office ... + Act as a liaison between principal investigators and sub-investigators on regulatory issues and protocol changes. + Collaborate with the principal investigator to… more
    Actalent (08/16/25)
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  • Lead Project Engineer

    Fujifilm (Trenton, NJ)
    …+ Comply with all applicable US Food and Drug Administration (US FDA ) medical device regulatory requirements, applicable ISO 13485 standard requirements and ... level of customer satisfaction. + Adheres to the Company's quality and regulatory compliance requirements, without exception, and ensures that all job duties… more
    Fujifilm (08/13/25)
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  • Senior Manager/Associate Director - Commercial…

    Novo Nordisk (Plainsboro, NJ)
    …the Lead. Includes directing US media and advocacy strategies for Food & Drug Administration ( FDA ) advisory committee meetings + Measurement + Designs and ... Ensures all programming is done compliantly, with close partnerships with legal, regulatory , compliance and medical + Pipeline Communications + Accountable for the… more
    Novo Nordisk (08/12/25)
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  • Sr Clinical Consultant, MI I

    Fujifilm (Trenton, NJ)
    …+ Comply with all applicable US Food and Drug Administration (US FDA ) medical device regulatory requirements, applicable ISO 13485 standard requirements and ... and/or HCUS's future business activities. + Adheres to the Company's quality and regulatory compliance requirements and ensures that all job duties inherent in the… more
    Fujifilm (08/11/25)
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  • Sr Tech Support Engineer MI -2

    Fujifilm (Trenton, NJ)
    …+ Comply with all applicable US Food and Drug Administration (US FDA ) medical device regulatory requirements, applicable ISO 13485 standard requirements and ... to work on customer systems. + Adheres to the Company's quality and regulatory compliance requirements, without exception, and ensures that all job duties inherent… more
    Fujifilm (08/08/25)
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  • QA Lead Technical Operations - CAPA

    Sokol Materials & Services (Skillman, NJ)
    …and some project management experience. + Knowledge of biotech, bulk drug substance or finished product manufacturing, medical device analytical testing ishighly ... integrity principles + Proven attention to details + Comfortable working in an FDA regulated environment. About the Role DUTIES AND RESPONSIBILITIES: * Provide QA… more
    Sokol Materials & Services (07/31/25)
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  • Radiology Service Engineer III

    RWJBarnabas Health (West Orange, NJ)
    …radiology emergency on-call program. Staff assists management in meeting regulatory requirements and department/organizational goals. Performs other duties as ... + Assist Manager in maintaining and fulfilling the department/organization's regulatory requirements and goals. Complies with system, hospital and departmental… more
    RWJBarnabas Health (07/25/25)
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  • Senior Technical Support Engineer, MI - I

    Fujifilm (Trenton, NJ)
    …+ Comply with all applicable US Food and Drug Administration (US FDA ) medical device regulatory requirements, applicable ISO 13485 standard requirements and ... to work on customer systems. + Adheres to the Company's quality and regulatory compliance requirements, without exception, and ensures that all job duties inherent… more
    Fujifilm (07/16/25)
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  • 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 ... Chair and Senior Research Administrator to keep abreast of regulatory and legislative requirements related to research + Facilitate...+ Paid Time Off (PTO) + Medical and Prescription Drug Insurance + Dental and Vision Insurance + Retirement… more
    RWJBarnabas Health (06/06/25)
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