Mieke Roels is an experienced regulatory affairs professional specializing in CMC activities for both small and large molecules across European and international territories. Mieke's career includes roles at Janssen Pharmaceutica, Ardena, Sanofi, and UCB, where they provided strategic guidance on global CMC submissions and led regulatory initiatives. Currently serving as Associate Director of Regulatory CMC for Innovative Biologics at Sanofi, Mieke demonstrates strong team collaboration and problem-solving skills. They earned a Master’s degree from Vrije Universiteit Brussel in 2004.
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