职位描述
工作地点：广东中山市
工作性质：全职
性别要求：不限语言：精通的英语，精通的其他
岗位职责:
1 Performing analysis test of FP, ST and FUST according to Novartis Control procedure and local registration analytical methods strictly, supply accurate results in time.
2 Carry out analysis for process validation of product.
3 Conduct special analysis investigation, method development and validation.
4 Conduct those urgent tests and work to be required by supervisor.
Special Tasks
1 Revise related GLP/SOP according to Novartis Quality Policy as well as local regulatory requirements as arranged by supervisor.
Others
1. Ensure all activities in line with cGMP.
2. Observe BNP SOPs and be punctual according to working time schedule.
3. Keep assigned working place clean and tidy all the time.
4. Economize on water, electricity, solvent and others in work.
5. Strong team spirit and positive toward working attitude.
6. Attend to any other work related assignment, which may be given by supervisor.
任职条件:
制药及相关专业，大专以上学历；
5年以上QC理化分析经验；经验稍弱者可应聘质检技术员。
熟悉各种分析仪器；
熟悉GMP相关知识；
沟通良好。
其它福利:
班车及午餐
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