Our client is a US-headquartered multinational medical device business with a market-leading presence across multiple healthcare disciplines. The business runs in a state of perpetual innovation, continually developing new technologies and enhancing the patient experience. Due to their continued growth, they are now looking for a Regulatory Affairs Specialist to join their Dundee office.

As a Regulatory Affairs Specialist you will be primarily responsible for the administration and development of the Switzerland Person Responsible for Regulatory Compliance (PRRC) and UK Responsible Person (RP) activities within the company's diagnostics division according to appropriate procedures and processes. 

Key responsibilities: