深圳招聘

关键职责
1. 制作/审核/汇总产品批签发所需的文件（例如CC5…等）.
2. 完成上级主管或本部门负责人委派的其他工作。

关键技术能力以及其他弹性技能:
1. 大专以上院校毕业生或毕业班；药学或生物学相关专业背景；
2.有一年或以上药品质量检验经验或药品生产经验优先。
3. 具备GMP、药品法规的知识, 药物分析或药品生产相关知识；
4. 良好书写能力和文件管理能力者优先；
5.计算机技能：至少掌握Word、Excel和Outlook操作；
6. 责任感、团队合作精神和组织纪律性。

Key accountabilities
1. Prepare/review/compile the documents needed for batch release of products (such as CC5/BRP… etc.).
2. Any other work assigned by the superior or SQO head.

Key technical competencies and soft skills:
1. The graduate or near graduate from college above, pharmaceutical and /or biological related background;
2. One or above year or related experience on position of Quality or Production in Pharmaceutical company is advantage
3.Knowledage on GMP, pharmaceutical regulatory, pharmaceutical analysis or drug production are necessary.
4.Good writing skills and good practice on documentation is advantage;
5.Computer skill: Word, Excel and Outlook at least;
6.Responsibility, team-work and discipline.

深圳赛诺菲巴斯德生物制品有限公司诚聘