Maud Giorgi

Maud Giorgi is an experienced regulatory affairs and quality management professional with a robust background in the medical devices and consumer products industries. Currently serving as Associate QMS & Regulatory Affairs Director EMEA at Helen of Troy since September 2018, Maud provides regulatory insight, develops compliance strategies, and oversees obtaining and maintaining EMEA market authorizations across various product categories. Prior roles include Senior Regulatory Affairs Manager at Bracco Injeneering, where responsibilities included worldwide market authorizations and risk management, and Quality Manager at Swiss Medical Care, focusing on supply chain activities and product release. Maud holds a PhD in Evolutionary Biology from the University of Lausanne and multiple degrees in biology and teaching, complemented by specialized training in quality and regulatory affairs specific to the medical devices industry.