- We are looking for an ‘International Regulatory Affairs Specialist’ for our client operating in the medical device industry.As an International Regulatory Affairs Specialist, you will be responsible for ensuring that medical devices comply with global regulatory requirements, including FDA, EU MDR, and ISO standards. You will manage regulatory submissions such as 510(k), PMA, and CE Marking applications, and serve as the point of contact with regulatory agWe are looking for an ‘International Regulatory Affairs Specialist’ for our client operating in the medical device industry.As an International Regulatory Affairs Specialist, you will be responsible for ensuring that medical devices comply with global regulatory requirements, including FDA, EU MDR, and ISO standards. You will manage regulatory submissions such as 510(k), PMA, and CE Marking applications, and serve as the point of contact with regulatory ag
