Job Responsibilities:

A. Cooperate with the team in the reliability design, research and control of the in vitro diagnostic reagent quality management system and system in accordance with GMP specifications and ISO system requirements;

B. Supervision and implementation of in vitro diagnostic reagent quality technical regulations;

C. Follow up to maintain the effective operation of the in vitro diagnostic reagent quality management system;

D. Follow up the annual audit plan to supervise, audit and maintain the in vitro diagnostic reagent management system.

job requirements:

A. College degree or above.

B. Have work experience in biochemical reagent production, registration, quality system, and understand the relevant countries and local policies of Guangdong Province for the registration of in vitro diagnostic reagents.

C. Familiar with GMP regulations and ISO quality system regulations of biochemical reagents is preferred; those with ISO internal auditors who have written documents are preferred.

D. Good expression, communication and coordination skills.

E. Have excellent learning ability and sense of responsibility.