Frederic Charlier possesses extensive experience in quality assurance and operational management within the pharmaceutical industry. Charlier began a career at Eli Lilly and Company as a QA Representative focused on QP certification, followed by a role as a QA Project Engineer at Pharmacia/Pfizer, where expertise in GMP and sterile manufacturing was gained. In 2007, Charlier joined UCB Pharma as Production & Scheduling Manager, overseeing a drug product production team, before taking on various roles including QA Manager for Quality Management System and Audit Activities, Site Metrology & Validation Manager, and currently serving as External Manufacturing Lead - Associate Director, responsible for managing global contract manufacturers and strategic vendors. Charlier holds a Master’s degree in Pharmacy from Vrije Universiteit Brussel and is a certified QP.
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