Jason Liang , our Quality Assurance Director, has 15+ years of QA / RA experience in medical device / IVD.
Jason Liang is the Quality Assurance Director of China Med Device. He has 15+ years of QA/RA experience in medical device/IVD. He has held QA and RA management positions in several international corporations including Philips, Intertek, and TÜV Rheinland.
Jason is veteran auditor of medical device/IVD QMS for both international and domestic manufacturers in China. He is an expert on ISO 13485, QSR 820, China cGMP and understands the QMS dynamics between China, US, and EU. He has performed audits on a wide range of manufacturers in medical devices and IVDs (active, non-active), such as GE, Shimadzu, Fukuda, Panasonic, and many China domestic manufacturers.
Jason is a seasoned QMS trainer. His major training experience includes:
- ISO 13485 QMS training;
- European IVD Directive 98/79/EC, medical device Directive 93/42/EEC, and Directive 2007/47/EC training;
- Application of ISO 14971 risk management, including assessment of essential performance for IEC 60601-1 3rd edition;
- Application of IEC 62366 medical device usability; and
- China cGMP training.