Joanna Rakowska

Joanna Rakowska has a background in administrative roles and quality regulatory work in various companies. Joanna has experience in managing regulatory technical files, coordinating medical device regulatory activities, and providing support for implementing regulatory requirements. Joanna has also worked as a Key Account Assistant, Office Administrator, and Quality Business Analyst & Deputy RP; MDR Coordinator. Joanna holds a Certificate in Science GMP & Regulatory Affairs and a Bachelor of Science in Administrative Law.