Within the Regulatory Affairs department, you support the 3 Regulatory Affairs Project Managers by taking charge of the following main missions: - compile files (registrations, renewals, variations, etc.) - help in the preparation of renewals of regulatory files - prepare, send and follow all kinds of documents sent for legalization - order the Export samples, prepare their shipment and send - archive and monitor the regulatory basis - prepare the labeling texts and follow the translations - prepare deposits of promotional documents - archive the files for the preparation of promotional documents - order the Free Sale Certificates - archive training materials and update monitoring tables
Scientific training of minimum Bac + 3 level, you have more than 5 years of experience in Regulatory Affairs in the field of medical devices and drugs (mastery of cosmetics, food supplements and everyday consumer products would be a plus ) internationally, possibly in France and the EU. With a good knowledge of the constitution of technical files, registration files and variations in an international context, you have a good command of the Office Pack. You know how to show initiative and autonomy in your area of responsibility and you are able to adapt to different professional contexts. A strong sense of teamwork is required and English required.