• Integra LifeSciences (Plainsboro, NJ)
    …associate will perform all required duties in compliance with company policies, US Food and Drug Administration and DOT/IATA, ISO 13485, and other applicable ... accuracy in ORACLE. + Process all required receiving paperwork; affix all appropriate labeling to stock items. + Sort and distribute miscellaneous items received to… more
    DirectEmployers Association (11/07/25)
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  • Integra LifeSciences (Plainsboro, NJ)
    …associate will perform all required duties in compliance with company policies, US Food and Drug Administration and DOT/IATA, ISO 13485, and other applicable ... accuracy in ORACLE. + Process all required receiving paperwork; affix all appropriate labeling to stock items. + Sort and distribute miscellaneous items received to… more
    DirectEmployers Association (09/13/25)
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  • Associate Director, Regulatory Affairs…

    Gilead Sciences, Inc. (Parsippany, NJ)
    …Other Requirements** + In-depth understanding of US Food & Drug Administration (FDA) and European Medicines Agency (EMA) regulatory requirements and ... regulatory authorities. You will oversee preparation and maintenance of regulatory submissions, regulatory labeling and packaging for assigned products or… more
    Gilead Sciences, Inc. (10/23/25)
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  • Medical Information Manager, Innovative Medicines

    Teva Pharmaceuticals (Parsippany, NJ)
    …(sales detail aid, slide decks, websites, patient materials, etc.) meet the US Food and Drug Administration (FDA) Code of Regulations and guidance documents, ... and work closely with key members of internal departments including, Legal, Regulatory Affairs, Marketing, Global Health Economics, Value and Outcomes (Global HEVO),… more
    Teva Pharmaceuticals (10/29/25)
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  • Associate Director, PV Sciences

    Taiho Oncology (Princeton, NJ)
    …and/or leading a cross-functional team is a plus. + Expertise in relevant food and drug administration (FDA), European union (EU) and international conference ... Sheets, + Investigator Brochures, clinical summary of the NDA/MAA and product labeling and other applicable documents for clinical trials. + Evaluate current… more
    Taiho Oncology (11/04/25)
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