Global Regulatory Affairs Lead - Medical Devices
Cynosure, Inc
Cynosure Inc. is seeking a regulatory professional to lead complex submissions and guide product development through regulatory strategy.
Based in Westford, MA, you will collaborate with cross-functional teams to ensure compliant, timely filings for US and international markets. Required are 5–8 years in regulatory affairs for medical devices, strong knowledge of FDA/IVD regulations, and a proven ability to manage multiple priorities while meeting deadlines.
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