工作职责:
1、管理车间的物料、半成品、有效控制损耗率，做好生产结束后工器具的清点、归位及记录工作。
Manage workshop materials, semi-finished products, effectively control the attrition rate, and do a good job of the inventory, positioning and recording of tools after production.
2、按GMP和EHS的要求进行生产活动、及时填写相关记录。对现场、设备和环境进行维护，确保所有设备状态***，出现问题及时与维修人员联系。
Carry out production activities according to GMP and EHS requirements and fill in relevant records timely. Maintain the site, equipment and environment to ensure that all equipment is in the best condition and contact the maintenance personnel if there is any problem.
3、做好车间的生产安排，持续改善，提高生产效率。
Make production arrangement in workshop, improve production efficacy continuously.
4、参与相关文件的编写工作，使得文件比较高的可操作性。
Participate in the preparation of relevant documents, make the documents relatively high operability.
5、按要求参与GMP培训，配合内部、外部审计。
Participate in GMP training as required and cooperate with internal/external audit.
6、按实际业务需要支持仓库打包，收发货等库内操作。
Support warehouse packing, receiving and delivering according to actual business needs.
7、严格遵守和执行公司所以的政策和程序。
Strictly follow and implement all company policies and procedures.
8、与部门同事和上级保持有效沟通，完成上级交代的其他工作。
Maintain effective communication with department colleagues and superior, complete other tasks assigned by superior.
任职资格:
1、中专及以上学历。
Technical secondary school or above.
2、制药学或者其他相关学科，或拥有制药工业或实际经验或培训经历。
Pharmaceutical or other related disciplines, or have practical or training experience in the pharmaceutical industry.
3、能看懂简单英文标识。
Can read simple English signs.
4、制药等相关行业就职1年以上，有药品包装或药品贴签的经验者优先。
At least 1 years working experience in pharmaceutical industry, drug packaging or drug labeling is preferred.