Aisa Tonix possesses extensive experience in quality assurance and microbiology within the pharmaceutical and medical device industries. Currently serving as QA Analyst III at Phyton Biotech since September 2021, Aisa oversees the Quality Management System for GMP facilities, focusing on equipment qualification and computer system validation. Previous roles include Quality Assurance Analyst II at Bureau Veritas Group and various senior quality analyst positions at Johnson & Johnson, where responsibilities included compliance oversight, validation processes, and ensuring best practices in storage and distribution of pharmaceutical products. Aisa is a graduate of Benemerita Universidad Autonoma de Puebla with a Bachelor’s Degree in Pharmacological and Biological Chemist and is currently pursuing a postgraduate degree in Validation Process in Pharmaceutical Sciences at Universidad Nacional Autónoma de México.
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