1. ISO13485 quality system imported into the company system 2. Medical Device Regulatory Planning 3. Coordinated with the R&D center and prepared required documents along with license applications 4. Developed product verification and evaluation of process 5. ISO13485 internal audit for active medical device Quality Management System

Institute of Biomedical Sciences, Academia Sinica 、Drug discovery for Triple Mutation EGFR non-small cell cancer 、Neutralized peptides selection of SARS-CoV-2 from Phage Display platform 、Publication: EMBO Mol Med (2021)13:e12828

、Respond for the sale of Life science and IVD products 、Develop and explore business opportunities in pathology laboratories 、Monitor competitor's activity within the territory 、Working cross-functionally with RA department to ensure in-house procedures comply with latest regulatory requirements 、Develop relationships with key accounts and general customers 、To understand laboratory workflow and procedure to support end customers with professional product knowledge

Urology Department 、Translation medicine research of cancer therapy (signal transduction, drug resistant, tumor microenvironment, angiogenesis, new pharmaceutical composition discovery , animal model) 、Publication: Cancer Res. 2015 Sep 1;75(17):3568-82. doi