1、Responsible for the design and selection of equipment, procurement tracking, program design, commissioning and verification of the preparation plant of the new plant. 

2、Responsible for inline commissioning and trial production of the production line of the preparation plant in the new factory. 

3、Engage in all required production tasks in accordance with GMP norms. 

4、Preparation production operations: semi-finished product preparation, bottle washing, filling, lyophilization, cap rolling, etc. 

5、Writing of SOPs, batch records, etc.

6, the writing of operational records such as batch records and equipment use records during production operations.

7、Pick-up of materials and use of equipment. 

8、Cleaning of GMP workshop. 

9、Reporting and recording of deviations in the production process.

10、Complete other work assigned by superiors.

1、College degree or above, majoring in pharmacy, biology and other related majors.

2、More than 4 years of college, more than 2 years of undergraduate sterile preparation workshop work experience; biological products, such as monoclonal antibodies and other production workshop operation experience; lyophilized products or pre-filled needle products production experience is preferred.

3、Ability to use various types of Office software, with certain English reading and writing skills.

4、Ability to bear hardships and work hard, good expression ability and strong communication ability.