Oura seeks a Senior Regulatory Affairs Specialist to drive regulatory strategy and operations for our SaMD portfolio. You will partner with quality, engineering, product, clinical, and legal teams to ensure compliant, efficient lifecycle management from development through post‑market.
The ideal candidate has 5+ years in regulatory affairs for medical devices or digital health, with software‑based product experience and strong documentation skills.
#J-18808-LjbffrSaMD Regulatory Lead — Drive Strategy & Submissions in Remote at Unknown Company
This position is listed as full time and onsite.