Senior Regulatory Affairs Specialist - US​/EU Med Devices

A medical regulatory consultancy based in Atlanta is seeking a Senior Regulatory Affairs Specialist to prepare regulatory submissions for medical devices in the U.S. and Europe. The role requires a B.S. degree in a life science or technical discipline, with 2 to 5 years of experience in medical device regulations. The ideal candidate will have strong communication and project management skills, along with knowledge of FDA guidance and ISO standards.

This contract position offers an opportunity to contribute to the advancement of medical innovations.
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