Christelle Scliffet

Christelle SCLIFFET is a highly experienced Regulatory Compliance Manager specializing in regulatory affairs and design at MACO PHARMA since April 2020, where responsibilities include regulatory strategy, QMS implementation, and project management. Previously, SCLIFFET served as a Certification Project Manager at GMED for thirteen years, overseeing CE marking portfolios and compliance evaluations for medical devices. Prior positions also include Quality/Regulatory Affairs Project Manager at SEPTODONT and roles in quality control and analytical development in the pharmaceutical industry. SCLIFFET holds a DESS Master in Management, Quality, and Sustainable Development from Conservatoire National des Arts et Métiers and a Maîtrise in Biochemistry from the University of Lille 1 Sciences and Technology.