工作职责：

1.负责GMP相关文件和记录的管理工作；

Be responsible for the management of GMP related documents and records

2.负责压缩空气、氮气质量检测；

Responsible for the quality inspection of compressed air and nitrogen;

3.负责对有关影响产品质量的因素进行监督，并负责问题的纠正、偏差分析处理以及相关过程的管理及风险管理；

Supervise the factors affecting product quality, and take charge of problem correction, deviation analysis and handling, as well as management and risk management of relevant processes;

4.负责现场质量监督工作及洁净室环境监测工作；

Responsible for on-site quality supervision and clean room environment monitoring;

5.负责原辅料、半成品、成品、包装材料及工艺用水的取样；

Take samples of raw and auxiliary materials, semi-finished products, finished products, packaging materials and process water;

6.负责公司的物料、产品放行，在产品放行前完成对批记录的审核，确保每批放行的产品符合相关法规、药品注册和质量标准；

Be responsible for the release of the company's materials and products, complete the review of batch records before the release of products, and ensure that each batch of products released complies with relevant regulations, drug registration and quality standards;

7.负责公司与质量有关计算机系统操作权限的审核。

Be responsible for the audit of the company's computer system operation authority related to quality.

任职要求：

1.有QA工作经验者优先考虑；

2.大专及以上学历；

3.熟练使用计算机办公软件，熟悉GMP管理要求；

4.善于沟通，工作认真仔细，态度积极努力

注：该岗位为现场QA，因工作需要跟生产部门出勤时间保持一致，能接受倒班再行投递，谢谢！