Vice President, Americas Quality Operations at Stallergenes Greer
Ms. Kelly Thomas has over two decades of cGMP hands-on industry experience in both pharmaceutical and medical device manufacturing operations. Her experience covers all Quality Systems; as well as, all areas of validation; including, process/product validation, facilities validation, CSV and 21 CFR Part 11, test method validation, equipment/automated processes and cleaning validation.
Utilizing strategic thinking, risk-based approaches, and Lean principles, she has demonstrated success in steering and managing complex projects within the pharmaceutical and medical device industries.
Time: 25th June 2019 10:30 AM PDT | 01:30 PM EDT
Model : FDAQ-9257
Time: 31st May 2019 10:00 AM PDT | 01:00 PM EDT
Model : FDAQ-9268