23andMe
Mark Pisaro, Ph.D. is a seasoned professional in quality assurance and regulatory affairs with significant experience across various leading biotech and pharmaceutical companies. Currently serving as the Director of Quality Assurance and Regulatory Affairs at 23andMe since May 2017, Mark has held notable positions such as Associate Director of Quality Assurance at Intarcia Therapeutics, and Senior Validation/QA Professional at The Quantic Group, Ltd, where expertise in validation and compliance was demonstrated. Previous roles include Principal for QA Computer & Automated Systems at Genentech and Manager of IT Security & Compliance at Gilead Sciences. Mark's academic background includes a Ph.D. in Linguistics from the University of Chicago, along with various degrees and certifications in related fields, showcasing a diverse educational foundation.
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