Tyfenn Joubert

Tyfenn Joubert has extensive experience in regulatory affairs and quality assurance, particularly within the pharmaceutical and healthcare sectors. Since April 2002, Tyfenn has held roles at Pierre Fabre Group, including responsibilities in equipment qualification, manufacturing process validation, compliance, and quality management systems. Prior to this, Tyfenn worked at Schering-Plough Research Institute, focusing on quality assurance for various production forms, and completed a pharmacy internship at a hospital laboratory, where immunological, microbiological, and parasitological analyses were conducted. Early experience included quality audits at Yves Rocher. Tyfenn holds a DESS in Laboratory Engineering for Biology and Biotechnology with a focus on Quality Assurance, and a Doctorate in Pharmacy, both from the Faculté de pharmacie de Nantes.