1.開發調整分析方法(HPLC, GC, IC…)，協助產品製程開發，分析方法之確校；2.執行實驗室設備3Q；3.研擬審查藥典相關產品規格及分析測試，建立藥典規格；4.操作化學分析儀器進行分析，協助產品放行…

1.Facilitate Lot disposition process, reviewing GMP docs and managing timelines；2. Support day-to-day Quality Assurance – Operations；3.Perform batch disposition activities within specified timelines…

1. Review and provide the technical recommendations for CMC documentation and Common Technical Document(CTD) dossier from a regulatory…