Jean Philippe Bizot Espiard

Jean Philippe Bizot Espiard is a skilled professional in regulatory affairs and medical device management with extensive experience in post-market surveillance and support. Currently serving as a Post-Market Surveillance Specialist at Distalmotion since February 2025, Jean Philippe has previously held roles including Regulatory Support Manager at Cytiva and Regulatory Affairs Specialist and Associate at SOPHiA GENETICS. Additional experience includes positions as a RA/QA consultant at Amaris, Regulatory Affairs Consultant at EFOR, and a Regulatory Affairs Intern at NeuroResp. Early in the career, Jean Philippe worked as a Sanger sequencing engineer at INSERM, specializing in retinitis pigmentosa. Educational qualifications include a Master’s degree in project management and innovation in biotechnology from the University of Montpellier and a Bachelor’s degree in life sciences for engineering from FGES.