Terry Wilhide

Terry Wilhide is the Director of Product and Process Improvement for Biologic Manufacturing at Sanofi, with 15 years of experience in cGMP commercial and clinical sterile drug product manufacturing. Previously, Terry held positions including Department Head of Technical Services and Validation Manager at Pfizer, where they managed validation services and led continuous improvement projects. Terry also worked as a Supervisor at Wyeth and as the Manager of Clinical Manufacturing at Pfizer, overseeing aseptic operations and regulatory compliance. Committed to data-driven process enhancement, Terry has consistently delivered critical projects on time while fostering strong collaboration across cross-functional teams.