EPM Scientific seeks an experienced Regulatory Affairs professional for a medical device robotics company. You will own day-to-day Regulatory Affairs activities, collaborating with Quality, Medical Affairs, Clinical Studies, and senior leadership to drive EU MDR compliance and CE Mark maintenance.
The role supports FDA activities as the business expands globally, with a focus on Notified Bodies, substantial change assessments, and international regulatory strategy.
📌 Regulatory Affairs Lead (Barcelona)
🏢 Epm Scientific
📍 Barcelona
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