Be responsible for the daily supporting work of the laboratory, serves as the backup administrator of LIMSQC of the laboratory, and be responsible for the validation of LIMS system update with the LIMS administrator, drafting and maintaining LIMS-related procedures, maintaining LIMS master data, training new LIMS users and managing user rights, investigating LIMS-related deviations and changes, etc. Support LIMS-related audit activities as an alternate LIMS Administrator;

Be responsible for the management of laboratory reagents and internal references, including procurement, warehousing and receipt, inventory management, regular stocktaking, and ensuring that QC timely calibrates internal references;

Support the management of laboratory documents and records to ensure that the QC management documents, procedures and records are clearly circulated and the records are applied and archived in time;

Support or coordinate laboratory EHS management, support internal EHS training, etc.;

Support laboratory audits and inspections;

Other relevant work arranged by leaders.

Pharmaceutical engineering, pharmaceutical analysis or biotechnology and other related specialties, with LIMS management or use experience， is preferred, with GMP laboratory work experience, biomedical industry work experience is preferred;

Good learning ability, patient and meticulous;

Excellent English reading and writing skills, excellent speaking skill is preferred;

Understand relevant requirements of cGMP/GLP and ICH;

Have team spirit, and have relevant project experience is preferred.