1. 25 years' experiences in pharmaceutical science, which including pharmacology, biochemistry and pharmaceutical analysis. 2. Experiences in managing chemistry lab and Bio-lab, which including cGMP compliance, lab employee training, troubleshooting, QC, method development and validation． 3. Experiences in cGMP compliance, ISO 17025 compliance, ISO 9000 compliance. 4. Experiences in drafting Uncertainty Budget Summary as required by ISO 17025. 5. Experiences in establishing… Show more 1. 25 years' experiences in pharmaceutical science, which including pharmacology, biochemistry and pharmaceutical analysis. 2. Experiences in managing chemistry lab and Bio-lab, which including cGMP compliance, lab employee training, troubleshooting, QC, method development and validation． 3. Experiences in cGMP compliance, ISO 17025 compliance, ISO 9000 compliance. 4. Experiences in drafting Uncertainty Budget Summary as required by ISO 17025. 5. Experiences in establishing quality standard & monograph development. 6. Expert in pharmaceutical analysis and analytical method development 7. Experiences in biochemistry, bioassay, bio-analysis and statistics. 8. Experiences in standard setting and critical quality attribute setting. 9. Experiences in reference standard testing and reference standard evaluation. 10. Providing state- of –the- art process analysis services 10.Always manage to foster a positive environment based on the value of being open, friendly, confident and happy. Show less

CMC Director