Roberta Cogoni

Roberta Cogoni is a Regulatory Affairs Specialist at Medacta International since July 2025, previously serving as a Medical Device Compliance Specialist at PQE Group from November 2021 to October 2025. Responsibilities included supporting quality system compliance and regulatory affairs, CE marking, EU notifications, technical documentation reviews, and updates to Quality Management System procedures. Additional experience includes working as a Pharma Consultant focused on Computer System Validation for pharmaceutical and medical device companies. Roberta's academic background includes a Master of Science in Biomedical Engineering from Politecnico di Milano and a Bachelor's degree in Bioengineering from Università degli Studi di Cagliari, complemented by practical experience at Ospedale San Raffaele and various projects related to healthcare improvement and research.