吴军,GMP 自由工作者,从事制药生产质量管理领域26年,其中13年在合资企业从事设备维修、生产操作、质量保证管理等基础工作,5年国内制药企业生产质量副总工作,参与2010版GMP修订和实施技术工作、药品生产与质量管理技术咨询、培训工作。目前从事药品生产质量管理技术中有关设施设计、质量保证技术、药品生产工艺技术转移与过程控制、药品生产环境控制与监测、GMP系统建立与文件编制等GMP技术领域的探索。
Wu Jun, GMP freelancer, engaged in pharmaceutical production quality management for 26 years during which he carried out basic work including equipment maintenance, production operation and quality assurance management in joint venture enterprises for 13 years and served as deputy general manager for production quality in domestic pharmaceutical enterprise for 5 years; participated in 2010 GMP revision and implementation technology, pharmaceutical production and quality management technology consulting and training. Currently engaged in facility design, quality assurance technology, pharmaceutical production process technology transfer and process control, pharmaceutical production environment control and monitoring, GMP system establishment and documentation etc in pharmaceutical production quality management technology and exploration of other GMP technology fields.