Sirpa Nuolimo

Sirpa Nuolimo is an experienced professional in regulatory affairs and project management within the pharmaceutical and medical device industries. Currently serving as Associate Director of Technology & Project Management at Bayer since August 2019, Sirpa focuses on IUS device development. Prior roles at Bayer included Regulatory Affairs Manager with significant responsibilities in local regulatory actions and EU-level submissions. Sirpa's tenure at Santen involved leading the Regulatory Affairs Team and managing EMEA product development projects for ophthalmics. With earlier experience at Oy Medfiles Ltd. and various other companies, Sirpa possesses comprehensive expertise in regulatory strategies, submission processes, and life-cycle management, complemented by a strong academic background with degrees in Pharmacy from the University of Helsinki and the University of Eastern Finland.