• Specialist - Regulatory

    Novo Nordisk (Plainsboro, NJ)
    …This individual works cross-functionally with internal and external departments on Regulatory Affairs labeling related issues. Relationships Reports ... The Labeling Specialist supports the development of labeling activities for all regulatory submissions. This individual collaborates cross-functionally… more
    Novo Nordisk (12/11/24)
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  • Senior Specialist , Regulatory

    Integra LifeSciences (Princeton, NJ)
    …pathways to advance patient outcomes and set new standards of care. The Sr. Regulatory Affairs Specialist is a seasoned senior professional role responsible ... in the US, EU, Canada and globally. The Sr. Regulatory Affairs Specialist is responsible...establishing labeling requirements per regulations and review labeling that requires regulatory review and approval… more
    Integra LifeSciences (12/19/24)
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  • Medical Information Specialist (Hybrid)

    CSL Behring (King Of Prussia, PA)
    …The Specialist collaborates with internal teams to align training and labeling materials with medical standards, represents Medical Affairs at conferences, ... **Summary:** The Medical Information Specialist is responsible for providing accurate, balanced, and...and mentor new Medical Information Specialists, fellows, and Medical Affairs staff. + Contribute to labeling updates… more
    CSL Behring (12/13/24)
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  • Senior Quality Assurance Supplier…

    Catalent Pharma Solutions (Philadelphia, PA)
    …at least four years of experience + Strongly preferred degree in Regulatory Affairs , Biotechnology, Manufacturing, Operations, Supply Chain, Engineering or ... **Senior Quality Assurance Supplier Specialist ** **Position Summary:** Catalent, Inc. is a leading...Supply Packaging. Catalent offers GMP secondary packaging and clinical labeling services throughout our global network. Packaging can be… more
    Catalent Pharma Solutions (12/13/24)
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  • Executive Director, Medical Specialty

    CSL Behring (King Of Prussia, PA)
    …MA team. + Partner with and share expertise with the _global_ functions of Medical Affairs , ABC, CRD, R&D, Regulatory affairs , Global Clinical Safety & ... Director, will lead the development and execution of Medical Affairs strategies and tactics in support of the US...clinical expert in the assigned TA(s). Provide input on labeling and regulatory strategy. Maintain in-depth understanding… more
    CSL Behring (11/22/24)
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