• Co -Op: Regulatory Affairs

    Haleon (Warren, NJ)
    …and + identifying emerging regulatory trends and evolving FDA expectations. **The Regulatory Affairs Co -Op Associate** The objective of the Regulatory ... providing visibility to potential gaps. In this role, the Co -Op Associate will be provided with the opportunity...wide format used for submissions to the FDA. The Regulatory Affairs Co -Op will be… more
    Haleon (09/10/25)
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  • Associate Director, Global Regulatory

    Organon & Co. (Jersey City, NJ)
    …Teams and regulatory single point-of-contact for products within Global Regulatory Affairs and outside. + Communicate new legislations, guidelines and ... entire life cycle of the drug. + Represent Global Regulatory Affairs within our company's internal committees...For more information about personal rights under Equal Employment Opportunity , visit: EEOC Poster EEOC GINA Supplement OFCCP EEO… more
    Organon & Co. (07/26/25)
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  • Senior Manager, Regulatory Affairs

    Haleon (Warren, NJ)
    … to be part of something special. **About the role** This **Senior Manager, Regulatory Affairs - OTC** has responsibility for end-to-end regulatory ... we're in control of. In an environment that we're co -creating. And a culture that's uniquely ours. Care to...similar discipline + Minimum 8 years of experience in regulatory affairs + Experience working on FDA… more
    Haleon (09/03/25)
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  • Associate Principal Scientist, Regulatory

    Organon & Co. (Jersey City, NJ)
    …questions per established business processes and systems. + Demonstrate an understanding of regulatory affairs and apply this understanding to the benefit of the ... Scientist (Associate Director) is responsible for developing and implementing Regulatory Chemistry, Manufacturing & Controls (CMC) strategies for assigned small… more
    Organon & Co. (07/22/25)
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  • Senior Principle Scientist, Regulatory

    Merck (Rahway, NJ)
    …+ Coordinate regional regulatory strategy and submissions through collaboration with Regulatory Affairs Europe (RAE) and local affiliate teams. + Provide ... brochures + Local registration study protocols for secondary markets + Represent Global Regulatory Affairs on internal committees (eg, DRC, ADT/PDT, EDT, LEAD)… more
    Merck (08/23/25)
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  • Manager, Regulatory Program Manager…

    J&J Family of Companies (Raritan, NJ)
    …closely with the Global Regulatory Leader (GRL) and partners across Global Regulatory Affairs as well as Project Management, Medical Writing, Clinical and ... of a Bachelor's degree is required, preferably in Life Sciences, Business Management, Regulatory Affairs or a related discipline. Advanced degree preferred. + A… more
    J&J Family of Companies (09/05/25)
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  • Regulatory Submission Lead

    Sanofi Group (Morristown, NJ)
    …actively contribute to issue resolution before filing dates are impacted + Act as Regulatory Operations Team expert providing subject matter advice on ICH, eCTD, ... and Policies throughout the lifecycle of the application. + Coordinate with Regulatory Operations external equivalent to develop milestones and timelines and… more
    Sanofi Group (09/06/25)
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  • Director, Regulatory Policy & Intelligence

    Organon & Co. (Jersey City, NJ)
    …Position** Leading the Regulatory Policy and Intelligence activities for Global Regulatory Affairs covering all Therapeutic Areas and products, as well as ... 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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  • Global Medical Director, Evidence Generation…

    Sanofi Group (Morristown, NJ)
    …+ Collaborate with glocal cross-functional teams including Medical TA, Clinical Development, Regulatory Affairs , HEVA, Market Access, and Commercial to align ... scientific exchange and engagement. We serve as key strategic partners for commercial, regulatory , R&D, market access and external affairs to develop and launch… more
    Sanofi Group (07/23/25)
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  • Global Senior Director Medical Affairs

    Merck (Rahway, NJ)
    …edge of therapeutic and patient care advances. The GDMA coordinates medical affairs activities to resolve regulatory , reputational, ethical, and other asset ... **Job Description** The Global Senior Director of Medical Affairs (GDMA) for Melanoma coordinates the development of...Sr. GDMA contributes substantially to and is a valued co -strategist on the Global Franchise Team and assigned Product… more
    Merck (09/12/25)
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