Tiffany Andrews

Tiffany Andrews is a Quality Documentation Specialist with extensive experience in product, equipment, qualification, and analytical method transfer and validation testing supporting cGMP manufacturing. They served as a QC Lab Supervisor and Senior Chemist at Wockhardt USA from 2004 to 2014, followed by roles as a QA Auditor at Fresenius Kabi and a QA Documentation Specialist at GlaxoSmithKline. Tiffany is currently a Senior Technical Writer at Vertex Pharmaceuticals, managing project documentation and overseeing the document management system (DMS) workflow. They hold a Bachelor of Science degree in Chemistry from the University of Illinois at Urbana-Champaign, earned in 1998.