Selena Smith

Selena Smith is a seasoned professional in Quality Assurance with extensive experience in the pharmaceutical and clinical laboratory sectors. Currently serving as Director of GCP Quality (Vendor Quality) at Regeneron Pharmaceuticals, Inc. since August 2020, Selena previously held the position of Associate Director of Clinical Quality Assurance at Vertex Pharmaceuticals, where responsibilities included managing the Cystic Fibrosis program's quality oversight and leading GCP QA audits. Earlier roles include Sr. Manager of Quality Oversight at PRA Health Sciences, where program development and inspection readiness were key responsibilities, and Sr. Manager of QA Auditing at Chiltern, with a focus on managing audit staff and regulatory inspections. Additional experience includes supervisory positions in clinical laboratories at Spectrum Laboratory Network and St. Joseph's/Candler, as well as foundational work as a Medical Technologist at Diagnostic Laboratory Services. Selena holds an MBA from Saint Leo University and a Bachelor's degree in Clinical Laboratory Science from Eastern Kentucky University.