• Master of Education (Leadership, Policy, and Change)

• Bachelor of Science (Chemical Science) (Hons)

• CQI & IRCA-certified Lead Auditor ISO 13485

• CQI & IRCA-certified Lead Auditor ISO 22000

For over 26 years in the GMP-regulated industry, Gloria has managed various quality system elements of the pharmaceutical and related industries, and was responsible for sustaining them to the required standards, including PIC/S, USFDA, EU, ISO, and ICH. She has an established track record of technical capabilities across diverse functions in the manufacturing and consulting sectors of the life sciences industry, such as Laboratory Controls, Quality Assurance, Auditing, Training, Regulatory Conformance, and Validation for the pharmaceutical and medical device companies. Her principal areas of expertise include Quality Systems, Laboratory Controls, Product Conformance Initiatives, Quality Assurance and GMP Upgrade Strategies, Quality Risk Management, and Validation. In addition, Gloria has conducted numerous third-party audits/gap analysis, and provided remediation strategies in facilities intended for the manufacturing of APIs, final dosage forms, and medical devices. Besides establishing compliance, Gloria has developed training programs related to ISO/GMP/GDP/G(QC)LP and delivered these courses for both local and overseas organizations across the Asia Pacific region. Gloria holds a Master Degree in Education (M.Ed.), majoring in leadership, policy, and change. In her consulting practices, Gloria places a strong focus on quality culture and sustainable compliance measures.