Simon Burlan

Simon Burlan is a seasoned professional in the pharmaceutical industry, currently serving as the SPMS Quality and Regulatory Drug Products Business Partner at Sanofi since October 2017. In this role, Simon manages the launch of monoclonal antibody products across various countries, implements the AQP process for biotech product launches, and contributes to Quality Agreements and Life Cycle Management projects. Prior to this, Simon held positions at Sanofi, Novo Nordisk, and Aspen Pharma, gaining extensive experience in validation management, compliance, and production optimization. Simon holds a Doctorate in Pharmacy and a Master’s in Industrial Management, complemented by a specialized master's in Pharmaceutical Industry Management from CentraleSupélec.