谢京军 罗氏诊断高级验证经理
谢京军有超过15年的制药和生物技术行业内的药品生产及咨询服务经验。目前他在罗氏诊断任高级验证经理，之前于恩宜珐玛(天津)工程有限公司担任调试与确认和GMP合规高级专家，曾担任过过项目质量经理、项目经理和质量经理。在加入恩宜珐玛公司之前，他在天津百特医疗用品有限公司担任过仓库主管、计划专员和生产主管，在博福-益普生(天津)制药有限公司担任过验证专员和质量保证工程师，具有药厂生产、质量保证、物流等方面的经验。他曾参与了许多工程投资项目，负责GMP合规、调试和确认执行。他是中国食品药品监督管理总局高级研修学院客座教授。也是国际制药工程协会中国理事会的理事。
Pete has more than 15 years production and consultant experience in pharmaceutical and biological industry. Now he is the senior validation manager in Roche Diagnostics，and he was senior specialist, commissioning & qualification and GMP compliance. He has been as project quality manager, project manager and quality manager. Before joining NNE Pharmaplan, Pete acted as warehouse supervisor, planner and production supervisor in Baxter. He also acted as validation specialist and QA engineer in Beufour-Ipsen. He had much experience in production, quality assurance and logistic. He has been involved in many engineering project and was responsible for GMP compliance, commissioning and qualification. He is the CFDA Institute of Executive Development and member of ISPE China board of directors.
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