Ignė Pleskutė currently serves as a Regulatory Affairs Expert at Oy Medfiles Ltd since June 2023. Formerly, Ignė held the position of Head of Product Quality at Ortho Baltic from November 2022 to May 2023, focusing on medical device documentation and compliance with legal standards. Prior roles include Senior Regulatory Affairs Specialist and Regulatory Affairs Specialist at Biomapas, where responsibilities involved project ownership and collaboration with marketing authorization holders. Additional experience includes a position as Regulatory Affairs Specialist at Teva Pharmaceuticals and Chief Specialist at the Marketing Authorisation Unit of the State Medicines Control Agency of Lithuania. Ignė holds a Master of Science in International Marketing and Management from ISM University of Management and Economics and a Master's degree in Pharmacy from the Lithuanian University of Health Sciences.
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