Karolien Mas

Karolien Mas is a seasoned professional in the field of regulatory affairs, currently serving as Manager of Regulatory Affairs CMC at BioNTech SE since February 2023. With previous experience as Associate Director of Regulatory Affairs at IQVIA, Karolien has expertly managed regulatory CMC projects for major pharmaceutical clients, handling clinical trials, new product registrations, and commercial product maintenance globally. This includes overseeing project teams across multiple regions and developing training programs. Karolien's background also includes roles at Genzyme, Hermoo Belgium NV, K.U.Leuven, and the University of Florida, involving extensive contributions to regulatory submissions, product development, and scientific research. Educational qualifications include an engineering degree in cell and gene biotechnology from KU Leuven.