Fiona Day is a seasoned professional in the field of Quality Assurance and compliance, currently serving as Associate Director GLP QA at Zymeworks Inc. since March 2024. Prior experience includes roles such as Oncology 3rd Party Quality Lead at Pfizer, Senior Manager GLP Compliance at Seagen, and Senior Consultant at ADAMAS Consulting. Fiona has developed expertise in GLP studies and FDA regulations through positions at PhenoPath and SNBL USA, where responsibilities included auditing and analytical study management. With a foundational background in scientific research from roles at Amgen, Corixa Corporation, and Immunex, Fiona holds a PhD in Biochemistry from the University of Glasgow and a Bachelor of Science with 1st Class Honors from the University of Strathclyde.
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