Lead Regulatory Affairs Specialist role in Barcelona with hybrid work flexibility. Drive day-to-day regulatory activities, ensuring EU MDR compliance, and CE marking for advanced robotic medical technologies. You will oversee Notified Bodies and shape general regulatory strategy under the QA & RA Director.
Ideal candidate brings EU MDR mastery, CE Mark experience, and readiness to contribute to US market regulatory planning in a fast-growing medical device company.
📌 Regulatory Lead – Medical Devices (Madrid)
🏢 Epm Scientific
📍 Madrid
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