深圳招聘

KEY ACCOUNTABILITIES
关键职责

1. Raw materials and Packaging materials tests and reports 15%
对原材料、包装材料进行测试和撰写报告

2. Drafting relative SOPs (including bulk flu project) 5%
起草相关的标准操作程序（包括流感新项目）

3. IPC, Intermediates, bulk and FP physico-chemical tests 50%
负责过程控制、中间产品、大罐和终产品的理化实验

4. Perform the validation of the analytical method 5%
分析方法的验证

5. Contribute to the qualification, calibration and maintenance of equipment and instruments 10%
仪器设备的确认、校准和维护

6. Sampling，Sample reception and distribution
取样，以及样品接收和分发5%

7. Any other work assigned by QC Mgr. / SQO Mgr. 10%
完成质控经理／质量部经理布置的其他任务


REQUIREMENTS
任职资格(Required education, experience, certifications, and competencies.)

－College qualification or above;
大学专科以上；

－Pharmaceutical or biological background, regulatory knowledge and GMP good understanding is prefer;
药学或生物学等相关专业，了解药品法规和熟悉GMP优先；

－At least one year of related experience on pharmaceutical test, experience on physic-chemistry tests is prefer;
一年以上的药品检验相关工作经验；具有理化检验经验优先；

－Experience on operation of HPLC and GC is prefer;
有HPLC和GC操作经验优先；

－Computer skill: word, excel at least;
计算机技能：至少掌握word, excel；

－English: Read and write is required, simple communication is advantage.
英语水平：必须具备读写能力，会简单的口语交流优先。

深圳赛诺菲巴斯德生物制品有限公司诚聘