She has been in the Pharmaceutical and Medical Device industry for 30 years. She has held APAC positions in Pharma companies such as Eli Lilly & GSK and was the Director of Clinical & Regulatory Affairs at Johnson &Johnson Medical Asia Pacific, pioneering premarket registration work on breakthrough technology in Medical Device. She was the Vice President of QA/RA for Asia Pacific and Greater China regions at GE Healthcare serving combined business size of $3.6B and Vice President of Regulatory Affairs at APACMed, sitting at the table with policy makers, advocating for a significant number of global MNC and local SME. Prior to joining Baxter, she was the Vice President, Regulatory & Government Affairs and Quality Assurance at Align Technology, Asia Pacific. She has built the QA/RA/GA team of the first Greenfield manufacturing plant in Asia. Led the team in setting up QMS from ground up and successfully obtained the product registration approval within one year.

Quan is currently the Vice Chair of GHWP and leads its Capacity Building initiatives contributing in the global effort of Medical Device Regulatory harmonization and convergence.

She holds a Master of Science in Clinical Pharmacy from The London School of Pharmacy, UK