Diana van Geenhoven

Diana Van Geenhoven is a seasoned professional in quality assurance and process development within the pharmaceutical and biotech industries. Currently serving as the Global Quality Cluster Lead at Centrient Pharmaceuticals, Diana oversees operational quality for FDA-registered production sites. Diana's extensive experience includes leadership roles at Teva Active Pharmaceutical Ingredients, where responsibilities encompassed quality compliance for APIs across various regions. Prior positions at Abbott involved managing product and process development, as well as technology and engineering departments for pharmaceutical operations. Diana's earlier career included directing quality affairs at DSM Biologics, contributing to biological API production, and leading development projects at Organon. Diana's foundational education includes a Master's degree in Chemical Engineering from the University of Groningen.