Regulatory Affairs Specialist, Medical Devices (EU/EXTRA-CEE)

A medical device manufacturer is seeking a Regulatory Affairs Specialist to assist in registering medical devices in EXTRA-CEE countries. Responsibilities include preparing regulatory documents, managing submissions, and ensuring compliance with EU regulations. The ideal candidate should have a Bachelor's degree in a scientific discipline and at least 3 years of experience in regulatory affairs in the medical device industry. Fluency in English is required for effective communication.