岗位职责 Job Responsibilities

83 遵守公司及部门的安全及质量手册，严格按SOP及分析方法进行实验操作
Abide by the Company's and Department's safety and quality manual, and carry out experimental operation in strict accordance with SOPs and analysis methods
83 完成进厂物料(原料，辅料，包材)及公用系统的测试任务，如实记录测试过程，报告测试结果
Complete the test of incoming materials (API, Excipients and Packaging Materials) and utility samples. Record the test process truthfully and report the test results
83 按批准的方案，执行分析方法确认工作
Carry out method verification according to approved protocol
83 完成进厂物料、水样、气体的采样工作
Complete the sampling of incoming material and utility samples02
83 及时汇报测试过程中的任何异常情况，参与相关调查。
Report the abnormal issue during the test in time. Participate relative investigation.
83 按SOP进行仪器维护和再确认(如： HPLC, UV,溶出仪，等)
According to SOP, perform the maintenance and requalification of instrument (HPLC, UV, etc.)
83 完成主管指派的其他职责。
Other duties as assigned by supervisor.

技能要求Required Skills

83 大专或以上学历，药学/化工/化学分析等相关专业
College degree or above, major in Pharmacy/Chemical/Chemical analysis or related subjects
83 至少2年及以上药品生产企业或相关行业QC 工作经验
At least 2 years of QC experience in pharmaceutical manufacturing or related subjects
83 熟悉QC常规仪器的操作，如：HPLC, UV, GC 等
Familiar with QC instrument operation, such as: HPLC, UV, GC, etc
83 熟悉中国药典，USP及EP
Familiar with Chp, USP and EP
83 熟练办公软件操作，良好的英文读，写能力
Skillful with MS software, Good command of read and written English