Inci Günler

Inci Günler is a seasoned professional in regulatory affairs with extensive experience across various companies. Currently serving as a Senior Regulatory Affairs Consultant at PQE Group since October 2024, Inci specializes in managing Electronic Common Technical Documents (eCTD). Prior roles include Sr. Regulatory Affairs Specialist at Baxter International Inc., where global regulatory strategy and delivery were key responsibilities, and Regulatory Affairs Associate at Teva Pharmaceuticals, focusing on marketing authorizations and regulatory life cycle management. Inci began the career as a Regulatory Affairs Specialist at SEDQ, supporting registration processes in compliance with European legislation, and has a strong academic background with a PhD in Organic Chemistry from Universitat Rovira i Virgili and a Master’s degree from Middle East Technical University.