Gillian Brodie

Gillian Brodie has extensive experience in the pharmaceutical and biotech industries, currently serving as Associate Director of Quality Compliance & Systems at Takeda since October 2017, with responsibilities including directing quality operations at a biological manufacturing facility and ensuring compliance with regulatory standards. Previous roles include GCMC Regulatory Manager at Pfizer, where Gillian developed CMC regulatory strategies for vaccines, and Technical Expert CMC at GSK Vaccines, focusing on technical regulatory documentation for lifecycle management. Earlier experience includes serving as Regulatory Affairs Associate at Servier, where regulatory activities were managed for multiple countries, and internships at O'Donovans Pharmacy. Gillian holds a Master of Pharmacy from the Royal College of Surgeons in Ireland and a Bachelor of Pharmacy from University College Cork.