Regulatory Affairs Officer
Current- Registration of Class III medical devices for the US and EU market.- Prepare and write registration dossiers.- Manage the maintenance of the US and EU licences and the follow-up of the registration files.- Evaluation of the changes (Change Control).- Define the regulatory strategy regarding the development of new products in collaboration with internal departments.- Prepare and support inspections conducted by Competent Authorities.- Watch monitoring of new regulatory requirements, interpretation and implementation.