Regulatory Export Assistant – France

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Job description

Responsibilities 

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

Profile

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.

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