Amin Ahidar

Amin Ahidar has an extensive work experience in quality assurance and regulatory engineering. Starting in 2010, they worked as a Quality Control Assistant at Servier, a Research Chemist at Université de Reims Champagne-Ardenne, and an Analytical Chemist at Université de Bordeaux. In 2011, they moved to Septodont as a Research and Development Engineer. In 2012, they became Quality Manager at IAV Automotive Engineering, where they coordinated the ISO 9001 certification project, helped define the Quality Policy and goals with top management, designed process maps and performed gap analysis, wrote and reviewed various QMS documents, and monitored the internal deviations and non-conformance process. In 2015, they began working as a Project Quality Consultant at EFOR, where they managed quality activities, verified the implementation of ISO 9001, ISO 13485, IEC 62304 and IEC 62366 requirements, planned and managed quality project milestones and deliverables, and managed Non conformities, CAPA and change requests. In 2016, they moved to Voluntis as a Project Quality Manager. In 2019, they became a Project Quality Engineer at Pixel Factory. Most recently, they are a Quality and Regulatory Engineer at FeetMe.

Amin Ahidar obtained a Licence in Biochimie from Université de Reims Champagne-Ardenne from 2006 to 2009. Amin then went on to receive a Master 1 in Chimie des Substances Naturelles et Médicaments from Université de Reims Champagne-Ardenne from 2009 to 2010. After that, they earned a Master 2 (M2) in Méthodologies Analytiques Appliquées aux Produits de Santé from Université de Bordeaux from 2010 to 2011. Lastly, they completed a Mastère Spécialisé in Management de la Qualité from Arts et Métiers ParisTech - École Nationale Supérieure d'Arts et Métiers from 2011 to 2012. In addition, they have obtained a Green Belt Certificate on Medical Device Regulation EU MDR 2017/745 from Easy Medical Device in November 2020 and a Mini-Course MDR 2017/745 from Easy Medical Device in October 2020.