• AI Solutions Manager, Life Sciences R&D…

    Deloitte (Morristown, NJ)
    …serve + Limited immigration sponsorship may be available Preferred: + Understanding of pharmaceutical regulatory data and regulatory filing requirements and ... analytics solutions + 4+ years of experience with Life Sciences Pharmaceutical R&D regulatory data lifecycle . Experience to include introducing new technologies… more
    Deloitte (01/15/26)
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  • Director, Regulatory Affairs…

    Stryker (Trenton, NJ)
    …disposition and release in addition to Quality Assurance responsibilities.Viewed as pharmaceutical regulatory expert within business. + Leads communication with ... aspects in external agency audits/inspections. + Stays abreast of external pharmaceutical regulatory requirements and expectations. **Education & Special… more
    Stryker (01/13/26)
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  • Director, Regulatory Affairs CMC

    Taiho Oncology (Princeton, NJ)
    … requirements and submission processes. + In depth knowledge of global regulatory requirements for pharmaceutical development and manufacturing. + Strong working ... our dynamic and expanding mid-size company in the role of Director for Regulatory CMC directly reporting to Executive Director, Regulatory CMC. Your expertise… more
    Taiho Oncology (12/09/25)
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  • Director, Oncology Business Development and Global…

    AbbVie (Florham Park, NJ)
    …years regulatory experience. Some portion may include experience related to pharmaceutical regulatory work (eg, other R&D role or specialized training). ... global regulatory strategies. + Preferred Experience: 10+ years' experience in pharmaceutical regulatory activities, with experience as lead regulatory more
    AbbVie (01/13/26)
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  • Sr. Manager, Regulatory Affairs Strategy

    Taiho Oncology (Princeton, NJ)
    …Knowledge, Skills, and Abilities: + Minimum of 5 years' experience working in pharmaceutical Regulatory Affairs + Experience with the development (IND/ CTA) ... Proposition: Join our dynamic and expanding mid-size company as a Sr. Manager, Regulatory Affairs Strategy. In this role, you will support submissions for various… more
    Taiho Oncology (12/13/25)
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  • Head of Global Regulatory Affairs, CMC…

    Sanofi Group (Morristown, NJ)
    …optimizing product approval pathways. The team develops and implements global regulatory strategies for pharmaceutical products, biologics, vaccines, and ... **Job Title:** Head of Global Regulatory Affairs, CMC Small Molecule **Location:** Morristown, NJ...into possible for millions. **Our Team/ Overview:** The Global Regulatory Affairs (GRA) CMC & Device Organization serves as… more
    Sanofi Group (12/22/25)
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  • Sr. Manager, Regulatory Affairs Cell…

    ThermoFisher Scientific (Cranbury, NJ)
    …and communicate the impact of relevant global regulations, guidelines, and evolving regulatory trends relating to pharmaceutical product development in the area ... helping find cures for cancer. **Discover Impactful Work** As a Sr. Manager, Regulatory Affairs, you will play a crucial role in interpreting and disseminating… more
    ThermoFisher Scientific (01/14/26)
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  • Associate Director, Regulatory Intelligence

    Otsuka America Pharmaceutical Inc. (Trenton, NJ)
    … intelligence and collaborates with SMEs to interpret the impact of regulatory changes to the pharmaceutical environment. **Job Description** + Oversee ... The Associate Director of Regulatory Intelligence leads the collection and dissemination of...new and updated regulations and guidance that may impact pharmaceutical practices, procedures and controlled documents. + Lead weekly… more
    Otsuka America Pharmaceutical Inc. (11/13/25)
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  • GRA CMC Lead

    Sanofi Group (Morristown, NJ)
    …within our GRA CMC & GRA Device Organization, you'll drive global regulatory strategies for pharmaceutical and vaccine products, collaborate with ... the CMC Lead role offers the opportunity to drive regulatory strategy for pharmaceutical products and vaccines across their lifecycle. Working at the… more
    Sanofi Group (01/14/26)
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  • Senior Manager, Product Artwork Automation

    J&J Family of Companies (Titusville, NJ)
    …technical standards related to artwork, including experience with international and pharmaceutical regulatory authorities. Knowledge & expertise in applying cGMP ... least 4 years' exposure to and general understanding of regulatory processes and systems and/or in pharmaceutical ...of regulatory processes and systems and/or in pharmaceutical packaging, artwork management, or related fields. + Strong… more
    J&J Family of Companies (12/23/25)
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