岗位职责： 1.Reports to a Group Leader or Lab Director during group leader absence 向组长或者实验室主管汇报实验结果及工作 2.Follows detailed project working plans or study protocols 按照详细的项目工作计划或者项目方案开展工作 3.Verifies, validates, or transfers new analytical test procedures and methods 验证新的实验方法或者转移来的新的方法方案 4.Complies with all relevant GLP regulations and guidelines while carrying out assigned studies, data analysis, interpretation and documentation 对于给定的项目必须遵循相关GLP法规要求，实验数据、记录等也要严格遵循相关法规； 5.Performs analytical testing, follows SOPs, performs instrument repairs and routine maintenance, prepares and reviews data packages, and writes reports or data package narratives 遵循公司SOP开展相关分析工作，能够熟练使用、维护以及修理相关仪器， 能够完成实验记录、报告、数据总结的准备和递交 6.Complying with statutory obligations, EH&S policy; Maintain tidy in their workplace; Use personal protective equipment properly 遵守相关法定义务，遵循实验室环境健康安全政策，维护工作台面整洁，正确使用有相应权限的仪器设备 7.QC documents related to large molecular projects, such as study data package, sample log in list, etc. 审核大分子项目相关文件，如数据文件包、样品入库清单等。 8.Draft or review QC validation data summary and / or sample analysis data summary. 起草或审核方法验证总结数据和/或样本分析总结数据。 任职要求： Speak, read, and write English. 熟练使用、阅读、书写英语 Major in biology, pharmaceutical science or related scientific discipline, bachelor degree or college degree. 生物、药学或者相关专业，本科或大专学历

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