Simone Antonini, MSc TÜV Rheinland Italia

After graduating with a MSc in Pharmaceutical Chemistry and Technology, Simone spent several years building experience in the pharma industry, working in production, validation and QA with parenteral drugs manufacturers.

He joined the medical devices industry in 2014, working in validation and QA for a leading Class III device manufacturer and finally taking a turn towards regulations.

Simone joined TÜV Rheinland Italia in March 2020.