Mike Portalios

Mike Portalios is a seasoned quality assurance professional with extensive experience in the pharmaceutical industry. Currently serving as a QA Analyst III at Teva Pharmaceuticals since August 2022, Mike is involved in the Change Control Board and acts as an EDMS system administrator, coordinating new product reviews and liaising among various departments including Regulatory Affairs, Packaging, Engineering, Production, and Laboratory. Prior to this role, Mike worked as a Technical Writer III at Actavis from January 2008 to July 2022, focusing on the transition of R&D products to commercial status and maintaining commercial master batch records and recipes in regulated systems. Mike's earlier career includes serving as a QA Lead at Tyson Foods and various pharmaceuticals from June 1985 to December 2007, where responsibilities included inspections, documentation for global supply, training for multiple positions, and microbiologic testing. Mike holds a Bachelor of Liberal Studies in Science and Professional Fields from the University of Iowa, earned between 1978 and 1984.