Andrew Huang

Andrew Huang is a seasoned professional with extensive experience in quality control (QC), quality assurance (QA), and manufacturing within the pharmaceutical and biopharmaceutical sectors. Since October 2018, Andrew has served as a Senior Associate at Lachman Consultant Services, providing independent consulting services that span QC data review, manufacturing and packaging batch records, deviation investigations, corrective action implementations, and GMP audits. Previously, Andrew worked as an Independent Consultant with Double Dragon Consulting Inc., focusing on GMP remediation for an international pharmaceutical company in Wuxi, China. Andrew's experience also includes roles as Associate Director of Analytical Services at Par Pharmaceutical, Director of Analytical Laboratory at Theracor Pharmaceuticals, Senior Scientist of Product Development at Eon Laboratories, and Manager of Analytical R&D Laboratories at Andrx Pharmaceuticals. Andrew holds a Ph.D. in Physical Organic Chemistry from the University of Minnesota.