Debbie Heng is a seasoned quality assurance professional with extensive experience in the medical device and pharmaceutical industries. Currently serving as a Senior Quality Assurance Specialist at PRO-TECH Design & Manufacturing, Inc. since December 2017, Debbie ensures compliance with ISO 13485, ISO 9001, and FDA regulations through internal audits and risk assessments. Previously, Debbie held multiple roles, including Owner of DPoon Quality Consultant and various consulting positions, where responsibilities included addressing FDA observations, conducting impact assessments, and managing quality systems. Notable past positions include QA Specialist at Hill-Rom and Quality Validation Engineer at Advanced Bionics. Debbie holds a Bachelor of Science degree in Molecular and Cell Biology from San Francisco State University and a Certificate in Forensic Identification from City College of San Francisco.
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