Suzanne Keating (Spence) is an accomplished professional in regulatory affairs with extensive experience in the pharmaceutical and medical device industries. Currently serving as Regulatory Affairs Senior Director at Viatris since July 2021, Suzanne oversees pre and post-approval regulatory affairs for a range of products globally. Previously, roles include Senior Scientist at GlaxoSmithKline, Regulatory Affairs Manager at Bioniche Teo and Mylan Institutional LLC, Regulatory Affairs Director at Viatris, and Senior Regulatory Specialist at Abbott Vascular. Suzanne holds a Bachelor of Science in Chemistry from NUI Galway and a Master of Science in Pharmaceutical Science from Kings College London.
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