工作经历 EMPLOYMENT EXPERIENCE |
2009.11 till now Austar Pharmaceutical Equipment (Shijiazhuang)LTD.
2009.11-至今 奥星制药设备(石家庄)有限公司 |
l AstraZenecaPharmaceuticals(China) Co., Ltd China Broad Market Manufacturing Site in Taizhou City
阿斯利康药业(中国)有限公司 泰州项目 OSD and SF Plant
口服固体和无菌灌装车间 | Project Manager项目经理 l This is a EMEA standard plant l 该项目要求达到EMEA标准 l Responsible for clean utility systems validation of OSD and SF plant l 负责口服及无菌灌装车间洁净公用工程的验证项目 l Take charge of compilation and execution guide of validation protocol l 主持验证方案的编写和实施指导 |
l Fresenius Kabi (China) Co., Ltd.
北京费森尤思卡比医药有限公司 (北京,口服车间) (Beijing, oral dosage plant) | Validation engineer验证工程师 l This is a EMEA standard plant l 该项目要求达到EMEA标准 l Responsible for water and clean gas system validation of EU standard oral dosage plant l 负责口服车间欧盟认证项目水及洁净气体系统的验证服务 l Take charge of compilation and execution guide of validation protocol l 主持验证方案的编写和实施指导 |
l Vaccine plant for Beijing Tiantan Yizhuang
北京天坛生物亦庄疫苗基地项目 (北京,生物制品,疫苗) (Beijing, Biological products, vaccine) | Validation engineer验证工程师 l Integral moving project for Tiantan Biological, with 2-3 billion investigation. l 天坛生物整体搬迁项目,投资20-30亿 l Chinese New GMP requirement, part products is for WHO certificate l 中国新版GMP标准,部分产品达到WHO水平 l Responsible for review of water system URS, FAT/SAT l 负责水系统URS审核,FAT/SAT审核 l Responsible for compilation of GMP review, SIA, RA, IQ, PQ for water system l 负责水系统GMP审核 SIA、 RA、 IO、PQ编写 l Responsible for training of water system validation l 负责水系统验证培训 |
l Harbin Pharmaceutical Group Co., Ltd. General Pharm. Factory
哈药集团制药总厂总体验证
(哈尔滨,无菌原料药和无菌粉针车间)
(Harbin, Sterile API and Powder for Injection Plants) | Validation engineer验证工程师 l HGPF project is EU certificate project l 哈药集团制药总厂认证项目为欧盟认证项目 l Including all validation activities for Sterile API and Powder for Injection Plants l 包括无菌原料和无菌粉针车间总体认证 l Project total investigation is more than 1.5 billions l 项目总投资在15亿以上 l Second design review of water system l 负责水系统二次设计审核 l Second design review of participate process pipe l 参与工艺管路二次设计 l Compilation and review of water system validation l 水系统验证文件的编写及审核 |
l Water system validation of Culture medium grade albumin in NCPC
华北制药集团培养基级白蛋白项目水系统验证服务 (石家庄,血液制品) (Shijiazhuang, blood produts) | Site manager项目经理 l This is a Chinese new GMP standard. l 该项目要求通过中国新版GMP认证 l Austar is responsible for validation service of water system/solution preparation system/clean air system in fermentation and purification plant l 奥星承担发酵及纯化车间水系统/配液系统/洁净气体系统验证服务 l Responsible for system commissioning and qualification, validation service execution l 负责系统的调试及确认、验证服务的实施 l Compilation of validation and 4Q protocol for clean pipeline system l 洁净管道系统验证方案,4Q方案的编写 |
l Shanghai Tasly
上海天士力药业有限公司 (上海,生物制药) (Shanghai, Biological products) | Site manager项目经理 l This is a biological products manufacturing and high technical company. l 上海天士力药业有限公司是一个以生产生物药为主 ,集生物药的科研、生产、销售为一体的高科技企业 l Austar is main responsible for water system renovation project, worked as project manager, overall responsible for project quality and schedule. l 奥星主要承担水系统的改造项目,任项目经理,全面负责项目质量和进度 l Responsible for gap analysis of water system renovation project, and RA, DIOQ compilation and execution. l 负责水系统改造项目的差距分析和改造方案的RA DIOQ的编写及执行 |
l Shandong Freda Biochem山东福瑞达生物化工有限公司 (山东,无菌原料药车间) (Shandong, sterile API plant) | Validation engineer验证工程师 l This is a FDA certificate project l 该项目为FDA认证项目 l Validation service scope include water system/ solution preparation system/ clean gas system in sterile API plant l 服务范围包括无菌原料药车间水系统/配液系统/洁净气体系统验证服务 l 负责制药用水水系统的调试及确认方案的编写及实施 l Responsible for compilation of commissioning and qualification protocol for water for pharmaceutical use system l 洁净管道系统验证方案,4Q方案的编写及审核 l Compilation of validation and 4Q protocol for clean pipeline system |
l 瑞阳制药有限公司 l Shandong Reyoung Pharma. (山东,冻干粉针,固体制剂) (Shandong, lyophilized powder, OSD plant) | 验证工程师 l 瑞阳制药拟通过中国新版GMP认证 l This is a OSD project with Chinese new GMP standard. l 负责口服制剂车间、冻干粉针车间水系统/配液系统/洁净气体系统调试及确认及洁净管道系统验证方案,4Q方案的编写及执行 l Responsible for qualification and verification of water system/solution preparation system/clean air system in oral dosage plant, lyophilized powder plant, and qualification protocol of clean pipeline system, compilation and execution of 4Q protocol |
l 华北制药华民药业项目 (石家庄,粉针制剂、口服固体制剂、无菌原料药、非无菌原料药) NCPC Huamin Pharmaceutical Project(Shijiazhuang, Powder for Injection, Oral Solid Dosage, Sterile API, Non-sterile API) | 验证工程师Validation engineer l 华北制药为亚洲最大的头孢类药品生产企业 l NCPC is the largest cephalosporin manufacturing company in Asia l 项目拟在2年内通过COS认证,要求验证服务达到欧盟标准 l This project is proposed for EU certificate. l 该项目的所有生产车间已顺利通过中国SFDA的2010版GMP认证检查 l All plant in this project have been approved by SFDA (GMP 2010 version) l 全面负责粉针制剂、口服固体制剂、无菌原料药车间的洁净公用工程系统验证工作 l Overall responsible for clean utility system validation of powder for injection, OSD, sterile API plant l 包括水系统及洁净气体系统设计GMP符合性审核,验证文件编写及调试监督,水系统及洁净气体系统测试项目的实施 l Include GMP conformance review of water system and clean gas system design, validation document compilation and commissioning supervise, execution of water system and clean gas system testing |
l 诺维信(中国)生物医药有限公司BHA项目 l BHA project of Novozymes (China) Biopharma Co.,LTD (天津,无菌原料药车间) (Tianjin biological product) | 验证工程师 Validation engineer l 诺维信(中国)生物医药有限公司是世界级领先的医药公司 l Novozymes (China) Biopharma Co.,LTD is the leader among pharmaceutical companies in the world. l The BHA project of Novozymes is designed according to standard of FDA. l Responsible for FAT, IOQ and RA compilation of CIP in sterile API plant.诺维信BHA项目完全按照美国FDA标准设计 l 负责诺维信无菌原料药车间CIP的FAT、IOQ及RA编写及执行 |
l 成都生研所再验证项目 l Revalidation project of Chengdu Institute of Biological Products (成都,生物制品) (Chengdu, Biological Products) | 验证工程师Validation engineer l 该项目为WHO认证项目,部分车间已通过WHO的预审 l This is a WHO certificate project, l 参与水系统及气体系统验证项目 l Participate in water system and clean gas system validation l 负责水及洁净气体系统验证的实施,文件的编写及审核 l Responsible for validation execution, document compilation and review for water and clean gas system |
2004.7~2009.10石药集团中润制药有限公司 2004.7~2009.10 CSPC Zhongrui Pharma |
l 研发课题组长 l Group leader of R&D | l 负责多个头孢品种的工艺研发项目 l Responsible for process R&D project for many cephalosporin products l 参与比啊培南项目研发及工艺验证编写及项目实施 l Participate in API R&D and process validation compilation and execution |
l 岗位工程师 l Process engineer | l 参与原料药车间技术改进及工艺变更验证 l Participate in technical improvement and process change validation for API plant |