Marc Vandervost is a seasoned professional with extensive experience in project management, regulatory affairs, and quality assurance within the pharmaceutical and biotech sectors. Notable positions include Project Manager at Lonza, where Marc led R&D projects involving chemical synthesized peptides, and Project Manager at NextPharma, overseeing the development of sterile drug products. Marc served as Manager, Commercial Cimzia QA at UCB, responsible for worldwide batch certification for a key biotech product, and held multiple roles at UCB that included managing contract manufacturers and leading technology transfer projects. Earlier experience includes roles at GlaxoSmithKline Biologicals and UCB Pharma, focusing on drug regulatory affairs and clinical research. Marc holds a Specialist degree in Industrial Pharmacy and a Master’s degree in Pharmacy from the Université Libre de Bruxelles.
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