Keya Mehta

Keya Mehta has extensive experience in quality assurance and validation within the medical device and pharmaceutical industries. Currently serving as a QMD Auditor for Norgine since September 2021, Keya's previous roles include QA Specialist at bioMérieux, QA Officer at ReBio Technologies Limited, and QA Specialist at MedPharm Ltd. Keya's expertise encompasses technical documentation, equipment validation, sterile system challenges, and compliance with GMP regulations. Notable contributions include managing quality management systems at Colorcon and validating processes and stability protocols according to regulatory standards. Keya's educational background includes an MSc in Formulation Science from the University of Greenwich and a Bachelor of Pharmacy from Rajiv Gandhi University of Health Sciences.