- This role involves leading regulatory affairs activities for medical devices in compliance with European regulations (EU MDR).
- The successful candidate will act as an expert in medical device classification, focusing on Class IIa and IIb.
Regulatory Affairs Specialist - Francisco Beltrão, PR - Amaris Consulting
Descrição
Regulatory Affairs Specialist
We are looking for a skilled Regulatory Affairs Specialist to join our team at Amaris Consulting.