Ana Misetic

Ana Misetic possesses extensive experience in regulatory affairs and quality assurance within the pharmaceutical industry. Currently serving as the Director of Regulatory Affairs, CMC at AbbVie since August 2012, Ana oversees the Quality Operations group, including responsibilities for QA Laboratory, Material Controls, Quality Control, and Batch Record Auditing. Previous roles at AbbVie include Director of QA and QA Operations Manager, along with managing laboratory teams to ensure compliance with cGMPs. Prior to AbbVie, Ana worked at Abbott Laboratories in various roles, including Project Manager for QbD Analytical and Regulatory Documents, and Senior Research Chemist in Analytical. Ana holds a Ph.D. in Chemistry from Loyola University Chicago, a BA in Chemistry from Northwestern University, and a Certification in Management Analytics from Lake Forest Graduate School of Management.