Joice Lee

Joice Lee is a certified Quality Engineer with 15 years of experience in the Medical Device and In Vitro Diagnostic Device industry. Joice applied knowledge of ISO 13485, MDSAP, and 21 CFR Part 820 throughout their career, holding positions such as Quality Assurance Engineer at Illumina and Senior Quality Assurance Specialist at Baxter International Inc. They also led various quality management and regulatory compliance initiatives during their tenure at Hill-Rom. Joice's expertise includes managing audit programs, CAPA programs, and post-market surveillance efforts.