You will prepare and draft documentation in view of obtaining marketing authorizations.
As the negotiating partner with the relevant regulation authorities, you will be responsible for
reviewing the documentation and dossiers on a regular basis and of monitoring regulations on the European level.
Bilingual French/English, you have a degree in pharmacy and a minimum of 2 to 3 years of experience in a similar position in a laboratory, a regulatory agency or a CRO. You will have had previous contacts with most of the international regulatory agencies (FDA, EMEA, PMDA…)




