We are looking for a Senior / Lead Regulatory Affairs Specialist to assist with the research, analysis and communication of information pertaining to the appropriate regulatory pathway for new or modified product. Reporting to the Regulatory Manager to ensure all the pre-market regulatory activities are performed and up-to-date, specific to the LATAM region. This is a hybrid role and would be based in our Sao Paulo office 2 to 3 days a week. About CMR Surgical CMR is an exciting and evolving co…