Sophie Dias

Sophie Dias currently serves as the Head of Regulatory Affairs & Design Quality at EOS imaging, where responsibilities include managing regulatory compliance for SaMD and X-Ray imaging systems and accessories classified from class I to IIb. Prior to this role, Sophie held the position of Head of Quality & Regulatory at SoftFil / Soft Medical Aesthetics, overseeing quality and regulatory matters for injection microcannulas, needles (class IIa), and cosmetics. Earlier experience includes serving as a Regulatory Affairs Specialist at Peters Surgical, focusing on surgical medical devices (class I to III), and as a QA/RA Assistant at BioSphere Medical SA, involved with embolization microspheres (class III). Sophie's career commenced as a Production Assistant at Cathnet Sciences, working with surgical medical devices (class IIa to III). Sophie holds a Master’s degree in sciences, technologies, and health with a specialization in service and systems engineering from Université de Technologie de Compiègne (UTC).