Lisa Cerven

Lisa Cerven is an experienced regulatory affairs and quality assurance professional with a career spanning over three decades. Currently serving as a Regulatory Affairs Project Manager at Perrigo Company plc since September 2008, Lisa is responsible for maintaining commercial Canadian product licenses and providing support for the annual kosher audit. Prior roles include Regulatory Affairs Annual Report Writer and Quality Assurance Technician at the same company, where responsibilities involved preparing FDA reports and implementing quality assurance measures. Previously, Lisa worked at Elan Pharmaceuticals as a Quality Assurance Release and Training Associate, focusing on batch record review and audits, and at Abbott Laboratories as a Quality Laboratory Technician & Training Coordinator, performing product testing and data evaluation. Lisa holds a Bachelor of Science in Biology from Grand Valley State University.