工作职责：
1.Perform production work of DP1 or/and DP2.
执行制剂一厂或/和制剂二厂的制剂生产工作；
2.Responsible for DS thawing, preparation, vial washing, sterilization, compounding, sterile filtration, filling, freeze-drying and capping.
负责原液解冻、生产准备、洗瓶、灭菌、配制、除菌过滤、灌装、冻干、轧盖工序；
3.Responsible for the preparation of disinfectants.
负责消毒剂的配制；
4.Responsible for the receiving and distribution of production materials.
负责生产材料的领取和发放；
5.Responsible for the cleaning and disinfection of rooms and equipment in the responsible area.
负责责任区域的房间和设备清洁和消毒；
6.Generate and review documents for related manufacturing processes.
起草和审核相关步骤生产流程文件；
7.Ensure operations strictly adhere to all QA-Controlled documents (such as SOPs, Batch Records) and cGMP/Quality requirements.
确保操作严格遵守所有QA控制文件（例如SOP、批记录）和cGMP/质量要求；
8.Clean and maintain the GMP facility and production equipment, assist to complete preventive maintenance of equipment.
清洁并维护GMP设施和生产设备，配合完成设备预防性维护；
9.Responsible for equipment revalidation and APS.
负责设备再验证和APS的执行；
10.Responsible for the submission requirements of the production materials for the post.
负责本岗生产用物料的提交需求；
11.Responsible for completing various trainings organized by the workshop and the company on time.
负责按时完成车间及公司组织的各项培训；
12.Ensure Safety manufacturing.
确保安全生产；
13.Ensure that drug product manufacturing conforms to written procedures of Chime biologics.
确保生产过程符合公司的书面流程；
14.Complete other tasks assigned by Immediate superior.
完成上级领导安排的其他任务。