Simon Burlan

Simon Burlan is a Quality and Regulatory Drug Products Business Partner at Sanofi, where they focus on the industrialization of biotechnological products and manage validation processes. Simon has previous experience as a stagiaire at Novo Nordisk, where they implemented the 5S methodology in the Washing and Sterilization sector. They also held roles in various pharmaceutical settings, including externships and internships, which strengthened their expertise in quality assurance and compliance. Simon earned a Doctorate in Pharmacy from the UFR des Sciences Pharmaceutiques de Caen and holds a Master’s in Business Administration from IAE de Caen and a specialized Master’s in Industrial Management from Ecole Centrale Paris.