1, responsible for the laboratory department team building, help the technical personnel to achieve technical growth target. 2, as a whole laboratory departments to carry out the testing work, optimizing the allocation of various resources in the laboratory, ensure that the work task is completed. 3, promote the standardization and standardization of laboratory departments work. 4, test and field sampling and the environmental protection industry as a whole management, and the detecting data rationality evaluation. 5, 10 years working experience in the third-party testing industry, 5 years working experience in management positions. 6, familiar with the laboratory assessment criteria aptitude and ISO17025 system, has the rich CNAS and CMA certification experience. 7, with the preparation of third party lab, gain the ability to CMA aptitude. Eight, all kinds of large-scale instruments are familiar with the laboratory operating procedures, familiar with all test sampling and analysis methods. 9, have strong ability of organization and management, coordination of communication skills. 10, intermediate engineer title (quality supervision and professional).

1.Review&check P&ID drawings according on site 2.Familiar and execute for validation protocols IC/OC/IQ/OQ 3.Supervise the preparation of Engineering file 4.Resolve analysis problem 5.Research and implment product quality, provide data for FDA, COS and China SFDA registration 6.Responsible and maintaining the QC analysis equipment 7.Responsible for the test project of research and development work 8.Responsible Utility&Process Validation task under Lead time 9.Consult &solved the validation problem that from client 10.Complete SOA,Installed resport and SAT resport 11.Installation and commissioning of Utility & Process Equipment’s（WFI,PUW,HAVC,process) 12.Responsible Validation Documents&Engineering Documents 13.Prepare and monitor availability certificate packages [certificate package , Baroscopic, Material certificate compilation ] 14.Responsible QA team,control validation status of FAT,DQ,IC,OC,IQ,OQ 15.Write protocol of Validation reference documents. 16.Responsible Hand over works of validation

2004.9 2012.2 chemical analysis center Director 2010 gain quality management engineer title 1. There is 8 years chemical lab operation and daily management,painting, chemical, physical and chemical test 2. ROHs&toys testing experience, familiar with the classification and separation of the sample. 3. Familiar with ROHS\REACH standards, and ASME EN. 4. Responsible for the test project of research and development work 5. Understand the laboratory controlled documents, lab quality manual, laboratory procedure rules 6. Plan to implement employee training,as well as to evaluate its performance 7. Plan system of equipment maintenance,during verification documents 8. Leadership work as assigned 9. Familiar with LC, GC and GCMS, such as UV, ICP equipment operation 10.Published 6 papers