ÂÜÀòÂÒÂ×

Cecile Begat is a Director of Quality Issue Management at Bayer, bringing over 21 years of experience in technical, quality, and managerial roles within parenteral dosage form manufacture, particularly in Biopharmaceutical and Radiopharmaceutical sectors. Previously, Cecile held positions at the Health Protection Agency, Novartis, and GE Healthcare, where responsibilities included managing quality systems, leading regulatory inspections, and certifying products. Cecile is a Qualified Person eligible under the Permanent Provision and has hosted and participated in MHRA and FDA audits. Educated at EABJM, Cecile has significant expertise in quality assurance, environmental monitoring, and GMP training.