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Global Regulatory Affairs Lead, Devices & Combo

Takeda, Cambridge, MA, United States


A global biopharmaceutical leader is seeking an Executive Director of Global Regulatory Affairs for CMC Devices and Drug-Device Combination Products. This hybrid position involves strategic leadership of global regulatory strategies, overseeing a team of subject matter experts, and working cross-functionally to ensure compliance and successful product approvals. Candidates must have an advanced degree in a scientific discipline, extensive experience in regulatory affairs and the medical device sector, and excellent communication skills. #J-18808-Ljbffr