必备条件:
3年以上化药QA/文件管理经验
能写文件，英文六级，稳定性强，不看异地人选
不要盲推，不写推荐理由直接拒绝，加萱萱微信 180 8124 8857 要项目手册
优先条件:
3年以上化药QA/文件管理经验
能写文件，英文六级，稳定性强，不看异地人选
不要盲推，不写推荐理由直接拒绝，加萱萱微信 180 8124 8857 要项目手册
岗位职责:
1. Complete the activties of quality management in every link of production, supervise the executing situation of SOP in the process of production.
2.Production site supervision and environment monitoring of production area.
3.Participate the quality activities of Quality Assurance dept .
4. According to specifed SOPs, manage and follow-up the deviations, change control and CAPA.
任职要求:
1. College degree in related majors or above.
2. At lease 3 years analysis experiences in QA.