1、根據GMP的法規，負責對實驗室溫控類設備的3Q驗證； Be responsible for equipment qualification work (IOPQ) following GMP regulation; 2、支持實驗室計算機驗證工作，使符合21CFR PART 11法規； Support labs computerize system validation job，which must meet 21CFRPART 11 requirement. 3、負責組內SOP、驗證方案報告模板的維護、確保符合最新法規要求； Be responsible for the maintenance of SOP, Protocol and report templateand ensure compliance with the latest regulations; 4、及時處理體系中存在的問題和不符合并組織修正，或及時反饋給各主管； Deal with the problems and noncompliance existing in the system, correctit or give feedback to the lab supervisor timely; 5、負責組內記錄格式及工作結果的審核，對檢測的準確性負責； Be responsible for the review of the format record and test result, andconfirm the data accuracy; 任職條件： 1、主修：化學、藥物、工程專業；本科或碩士學歷； Major: Biological, chemical, medicine, engineer; at least bachelor ormaster degree; 2、英語：至少四級； English: at least four level; 3、至少有3年GMP設備驗證經驗； At least three years’ experience on equipment qualification followingGMP regulation; 4、 熟練操作辦公室軟件； Familiar with office software; 5、很強的溝通技巧，細心，可以在壓力下積極工作； Strong communication skill, carefully. Work actively under pressure ; 6、團隊合作意識佳； Good sense on team work;