His past role as a validation department manager in a medical devices company leads Maxime to develop a strong experience with process validations, software validations, biological risk evaluation and transversal management skills. He has a good knowledge of european and US regulation.
Lately, he has been graduated with a MBA.
With over 10 years’ experience in medical device, Evelyne is specialized in design and development for medical devices and certified as an ICA auditor. Prior to joining DEM CONSEIL, Evelyne worked for an orthopaedic devices manufacturer. She has a good knowledge of european and US regulations.