英文简历翻译 goole英语翻译

英文简历翻译 goole英语翻译 英文简历翻译 goole英语翻译 Mainly be responsible for: 1, lead the team of QA to carry on producing the quantity management, the implement material, the middle product and the spot of the finished products supervise and control and let go, making produce the quantity process to match the norm of GMP, insuring the end product quantity. 2, Periodically organize the related working talent section to carry on the verification and verify again to Mr. with the system, equipments and the product crafts. 3, Attestation work of GMP:In work of three years, led the QA team help company to pass four times attestation of GMP, the supplier that the company passed many international archduke departments smoothly audits the attestation work on this foundation. 4, Be responsible for the quantity index sign that establishes the new raw material, new product, the document of GMP of the periodical emendation company. 5, Help the personnel of QC to carry on the maintenance to the precise instrument. Mainly be responsible for: 1, apply the new production craft in the actual production, insure normal production order(来自:WwW.ZW2.CN 爱作文 网:英文简历翻译 goole英语 翻译) and high quantity of the drugses. 2, Be responsible for all systems of document of GMP sorting and check the work, and the main plait wrote the production and quantity documents. 3, Verify the work:Be responsible for producing the craft and equipmentses to verify the project to establish, organize the implement and records to analyze the work. 4, Training of GMP:The GMP quantity that strengthens the employee realize. Mainly be responsible for: 1, standard research of new medicine quantity:Mainly carry on the HPLC to the content measurement method efficiently the liquid measureses the conditional research mutually. 2, The craft of the new medicine studies and declares to register the work:Include the craft parameter research of the new medicine and win to try and declare the registered related contents, and succeeded to obtain for the business enterprise 6 already have the approval text number of the national standard drugs. 3, The pharmaceutical factory declares the work:The establishment is applicable to the related management document of make the medicine business enterprise, the sorting reports the data, obtaining the drugs to produce the business enterprise permit for the business enterprise, carrying out the business enterprise from care the article factory toward the transformation of the pharmaceutical factory. Personal special features and advantage: 1, fast study ability:Can control the professional knowledge that new work post need quickly, the in time high quantity completes the work mission. 2, The good human relations exchanges ability:Can melt to go into a new environment more quickly, be in conjunction with the work with colleague. 3, Computer and network:Can quickly of automation transact and obtain the lately professional information. 11楼发布时间:2012-02-16