Global Regulatory Affairs Lead - CTD Submissions & Strategy
epm scientificNew York, NY
Global Regulatory Affairs Lead - CTD Submissions & Strategy
epm scientificNew York, NYManager L7
Electromedical and Electrotherapeutic Apparatus ManufacturingOther Scientific and Technical Consulting ServicesResearch and Development in the Physical, Engineering, and Life Sciences (except Nanotechnology and Biotechnology)
APPLY NOWEPM Scientific is seeking a Senior Regulatory Affairs Specialist to support regulatory compliance and submissions for marketed and development programs. You will contribute to regulatory strategy, health authority interactions, and global submissions while partnering with cross-functional teams in a fast-paced environment.
The role requires strong regulatory knowledge, ability to manage multiple priorities, and excellent communication skills to drive successful interactions with authorities
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Level
Manager L7
Location
New York, NY
Occupation
Regulatory Affairs Managers
Industry
Electromedical and Electrotherapeutic Apparatus Manufacturing
Posted
2 days ago