Laura Bourdin

Laura Bourdin currently serves as the Quality and Regulatory Affairs Manager at ZEISS Medical Technology, a position held since April 2019. Prior to this role, Laura held the position of Assistante QSE at ZEISS Group from October 2017 to March 2019, where responsibilities included the implementation of radiation safety management systems and ensuring compliance with CEFRI E certification. Earlier experience includes an internship in control at the Institut de Recherche Criminelle de la Gendarmerie Nationale, focusing on polymer studies and analytical methods. Laura holds a Master’s degree in Control and Quality from CY Cergy Paris Université and has specialized education in regulatory affairs for medical devices from Université Paris Cité.