Ms. 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
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.