Sara Rezouk

Sara Rezouk is a Medical Devices QA Engineer at QMD - DEGANIA I BIOMETRIX I ARTHESYS since July 2025, following experience as a Medical Devices Regulatory Affairs Officer at Horus Pharma from October 2024 to June 2025. In that role, Sara updated technical documentation for Class IIb medical devices in compliance with Regulation 2017/745 and contributed to design dossiers and risk analyses. Previously, as a Medical Devices Regulatory Affairs Intern at Horus Pharma, Sara assisted in similar regulatory tasks. Sara also worked as a Quality & Regulatory Affairs Specialist at DELTATEC SARL, where responsibilities included QMS implementation according to ISO standards and handling non-conformities. Additional roles encompass quality and hygiene management at Newrest and internships in various companies focusing on quality and HSE management. Sara holds a Master 2 in Ingénierie Qualité des Bio-produits from Université de Rouen and a Master in Analyse et Gestion Qualité from FST Settat.