EPM Scientific is seeking an experienced Regulatory Affairs professional for a medical device company focused on robotic technologies. You will own day-to-day Regulatory Affairs activities and work with Quality, Medical Affairs, Clinical Studies, and leadership to support general regulatory strategy.
You should have EU MDR expertise, CE Mark submission experience, and be comfortable engaging with Notified Bodies.
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📌 Global Regulatory Affairs Lead: Ivd & Software (Les)
🏢 Epm Scientific
📍 Les
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