(Senior) Regulatory Affairs Specialist Latvia

University degree in Life Science field. Fluent English and Latvian language. 4-5 years of experience in Regulatory Affairs with medicinal products. Experience in Regulatory Affairs with Medical Devices. Experience with food supplements and cosmetics is an advantage. Time management skills. Ability to solve problems and make decisions.

Act as Local Regulatory Affairs Specialist in Latvia. Manage registration and post-registration activities for Medicinal Products. Provide support for Medical Devices. Prepare and translate local documents. Communicate with Local Competent Authorities and client representatives. Perform regulatory review of promotional materials and product information. Translate/update product dossier documents. Ensure timely reporting and updating of regulatory data. Support clients with other RA tasks and provide regulatory advice.