Oura seeks a Senior Regulatory Affairs Specialist to drive regulatory strategy and operations for our SaMD portfolio. You will work across quality, engineering, product, clinical, and legal teams to ensure compliant, efficient regulatory activities throughout the product lifecycle. The role requires hands-on experience with medical devices or digital health, strong project coordination, and excellent communication.

Also on the board Same function, level within a rung

Level

Lead

Location

Brooklyn, NY

Occupation

Regulatory Affairs Specialists

Industry

Electromedical and Electrotherapeutic Apparatus Manufacturing

Posted

yesterday

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