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Senior Vice President, Global Regulatory Affairs
Sue Evans joined Aurinia in 2014 and serves as the Senior Vice President, Global Regulatory Affairs. Sue led the Aurinia submission team to a successful approval for LUPKYNIS®.
Sue has more than 25 years of experience in the pharmaceutical and biotech industry, spanning multiple roles across regulatory affairs, global program management, business development, process improvement, and analytical chemistry. She held various positions at 3M Drug Delivery Systems, working with large pharmaceutical clients including Sanofi, Nycomed, Novartis, and Schering-Plough. She also worked at Vectura (a UK Specialty Pharma company) as a regulatory specialist where she gained further experience in generics, asthma inhalers, and EU & U.S. regulatory affairs.
Sue earned an MBA from Vancouver Island University, a B.S. in Chemistry from Loughborough University, and is Regulatory Affairs Certified (RAC).