Louise Hardie

Louise Hardie (nee Croton) is an experienced quality assurance professional currently serving as Associate Director QA at Pharmaron since December 2017, where responsibilities include oversight of the Quality Management System (QMS) and Good Manufacturing Practice (GMP) compliance. Prior to this role, Louise held various positions at Bio Products Laboratory Limited, including Principal QA Advisor and Associate Principal QA Advisor, as well as Senior QA Officer at Clinigen Group, where Louise managed the QMS and served as Responsible Person under the Wholesale Distribution Authorisation. Earlier career roles include Quality and Technical Officer at Bupa Home Healthcare, focusing on GDP and pharmacovigilance training, and QA Laboratory Technician in environmental monitoring. Louise holds a Bachelor of Science (BSc) in Biology from The University of Nottingham and A Levels in Biology, Maths, and Geography from The Knights Templar School.