Julien Taburel

Regulatory Affairs Director

With an experience of more than 12 years in the pharmaceutical industry, Julien is a seasoned Information Technology Quality Assurance and validation expert. His experience at Novo Nordisk, Genzyme (Sanofi group) or as a consultant enabled him to acquire a deep knowledge of Pharmaceutics, Quality Management System, Data Integrity and Computer System Validation to comply with regulatory requirements from the US and Europe in particular. In his career, he also successfully led Regulatory Inspections and Corporate Quality audits. 

Julien holds a Master’s degree in Quality and Production Management from the University of Orléans.