Amelie Tedesco

Amelie Tedesco is a regulatory and compliance professional with more than 25 years of experience spanning pharmaceutical compliance, public health surveillance, laboratory science, and environmental toxicology. She currently serves as a Senior Compliance Specialist at Regeneron, where she drives compliance alignment across U.S., EU, and UK operations in accordance with global cGMP standards. Her responsibilities include auditing, supplier quality compliance, Change Control, CAPA, impact assessments, and audit readiness for supplier qualification and regulatory inspections.

In her role at Regeneron, Amelie has led the Supplier Corrective Action Report (SCAR) program, contributing to a 20% reduction in resolution and closure time. She also serves as a Change Control Owner, Workflow Author, Impact Assessor, and CAPA Owner, managing critical elements of the compliance lifecycle. Through cross-functional collaboration and coaching, she helps strengthen quality systems, promote continuous improvement, and develop sustainable compliance processes capable of meeting global regulatory expectations.

Before joining Regeneron, Amelie spent more than two decades with Health Research Inc. at the Wadsworth Center, where she worked as a Research Scientist supporting public health and clinical preparedness initiatives. Her work included method validation for the CDC Laboratory Response Network, root cause analysis, corrective actions, and advanced analytical testing using GC/MS/MS and LC/MS/MS instrumentation. She received the Commissioner's Excellence Award in 2016 for her contributions to public health initiatives. Amelie holds a Bachelor of Science in Chemistry from Siena College and completed a Public Health Fundamentals and Principles certificate through SUNY, where she subsequently entered an MPH track in Health Policy and Management.