The quality department consistently produces safe and high quality products, and completes the work of product quality inspection, raw material quality inspection, production supervision and equipment inspection and management.

The QA should assist the manager in establishing, standardizing, operating, and improving the quality management system; draft quality management documents, review the SOPs, process regulations, and quality standards drafted by various departments; supervise product production, testing, and storage processes; investigate deviations and changes; conduct on-site audits of material suppliers with relevant departments to evaluate supplier qualifications; conduct quality evaluations on raw materials and packaging materials; draft equipment verification plans and conduct equipment verification following the verification plan; complete equipment measurement/calibration management.

The quality department consistently produces safe and high quality products, and completes the work of product quality inspection, raw material quality inspection, production supervision and equipment inspection and management.

The QC Assistant should sample the materials and packaging materials and perform Physical and Chemical Analysis and Instrumental Analysis & Testing following SOP; conduct Physical and Chemical Testing of products and Stability Inspection samples; conduct purified water sampling, and conduct purified water physical and chemical testing in time according to SOP; draft equipment standard operating procedures and testing methods related to this position; complete cell growth test work; complete the reception and distribution of samples submitted for inspection; complete the cleaning and sanitation of physical and chemical laboratories; maintain daily instruments and equipment; fill in inspection records in a timely and accurate manner.

The Antibody-Drug Analysis Manager is responsible for the analysis of monoclonal antibodies, the management, maintenance, personnel training of the analysis equipment, and the establishment and verification of related analysis methods.

Verification Engineers establish the company's verification system; formulate and maintain quality system documents such as verification and verification processes, methods, and procedures; draft verification plans/verification reports, implementation tracking and verification reports for part of the commissioned supplier verification, write deviation reports during the implementation process.

The R&D department is our inventor. We develop new products, realize product production process transfer, configure Non-GMP liquid culture medium, develop customer-specific service projects, and conduct client-side technical communication. We constructed stable cell lines and improved the cell line culture process by docking with colleagues in the process team. Using innovative thinking, state-of-the-art facilities, and robust scientific methodology, we collaborate to discover the next breakthrough.

The R&D department is our inventor. We develop new products, realize product production process transfer, configure Non-GMP liquid culture medium, develop customer-specific service projects, and conduct client-side technical communication. We constructed stable cell lines and improved the cell line culture process by docking with colleagues in the process team. Using innovative thinking, state-of-the-art facilities, and robust scientific methodology, we collaborate to discover the next breakthrough.

The R&D department is our inventor. We develop new products, realize product production process transfer, configure Non-GMP liquid culture medium, develop customer-specific service projects, and conduct client-side technical communication. We constructed stable cell lines and improved the cell line culture process by docking with colleagues in the process team. Using innovative thinking, state-of-the-art facilities, and robust scientific methodology, we collaborate to discover the next breakthrough.

The R&D department is our inventor. We develop new products, realize product production process transfer, configure Non-GMP liquid culture medium, develop customer-specific service projects, and conduct client-side technical communication. We constructed stable cell lines and improved the cell line culture process by docking with colleagues in the process team. Using innovative thinking, state-of-the-art facilities, and robust scientific methodology, we collaborate to discover the next breakthrough.