Julie Mutert

Julie Mutert is a seasoned professional in regulatory affairs and quality assurance, currently serving as a Senior Manager of Regulatory Affairs at Galapagos since October 2017, where responsibilities include managing clinical trial applications and overseeing regulatory activities. Prior experience includes a role as a Quality Assurance Officer at Mylan Belgium, where Julie ensured the quality and compliance of medicine for the Belgian market. Julie's background also features positions at Pfizer - Altran BeLux, encompassing project engineering roles focused on clinical manufacturing and technology transfer, as well as engaging in regulatory submissions for biological products. Julie holds a Master's degree in Biomedical Sciences from KU Leuven and has completed a French Proficiency Course.