Kirubha Shangari Ilangovan is an experienced Regulatory Affairs Specialist currently working at Artivion EMEA since June 2023. Previous roles include Regulatory Affairs Specialist at ZL-Microdent Attachment GmbH from January 2022 to May 2023 and Regulatory Affairs Associate at QualiMed Innovative Medizinprodukte GmbH from January 2020 to November 2021. Initial experience includes work as a Regulatory Affairs Assistant and a Master Thesis Student at Fraunhofer IBMT, contributing to the HISENTS project focused on nanotoxicity screening technologies. Additionally, Kirubha undertook an internship at the DRDO BU-Centre for Life Sciences, working on a project in nanobiotechnology, and completed a Bachelor Thesis on fabricating chitosan-TiO2 nanocomposites. Academic qualifications include a Master of Science in Biomedical/Medical Engineering from FH Aachen University of Applied Sciences and a Bachelor of Engineering in Biomedical/Medical Engineering from Sri Ramakrishna Engineering College.
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