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1.嚴(yán)格按照公司的質(zhì)量體系要求工作，并不斷完善質(zhì)量體系。2.負(fù)責(zé)審核已執(zhí)行批記錄，如審核生產(chǎn)操作和工藝要求的一致性和符合性。3.負(fù)責(zé)生產(chǎn)關(guān)鍵日志的審核。4.協(xié)助物料處理。5.協(xié)助客戶審核/檢驗(yàn)準(zhǔn)備工作。6.完成直線經(jīng)理/主管分配的任務(wù)。1.Work strictly in accordance with the company's quality system requirements, and continueto improve the QMS .2.Responsible for review of Executed Batch Records, such as reviewing the consistency andcompliance of production operations and process requirements.3.Responsible for production critical logbook review.4.Assist in material disposition.5.Assist in customer audit/inspection preparation.6. Complete the tasks assigned by line manager/supervisor.1、生物技術(shù)、制藥、制藥工程等相關(guān)專業(yè)本科以上學(xué)歷;。2、2年以上藥品生產(chǎn)或質(zhì)量保證工作經(jīng)驗(yàn)，有生物治療工作經(jīng)驗(yàn)者優(yōu)先。3、熟悉 NMPA、 EMA、 FDA 藥品生產(chǎn)質(zhì)量相關(guān)法規(guī)，有良好的 GMP 理解和執(zhí)行能力。4、良好的溝通能力和團(tuán)隊(duì)合作精神。5、工作認(rèn)真，細(xì)心，責(zé)任心強(qiáng)，積極主動(dòng)，服從安排。6、良好的英語聽說讀寫能力1.Bachelor degree or above in related majors such as biotechnology, pharmacy orpharmaceutical engineering.2. More than 2 years of work experience in drug production or quality assurance,biopharmaceutical work experience is preferred.3.Familiar with NMPA, EMA, FDA drug production quality related regulations, have goodunderstanding and implementation ability of GMP.4.Good communication skills and teamwork spirit.5. Working conscientiously, carefully, having strong sense of responsibility, and shall beproactive, and obey arrangements.6. Good English listening, writing and speaking skills.上班時(shí)間：8:30-12:00；13:00-17:00；周末雙休，有班車接送上班地址：廣州市黃埔區(qū)九佛建設(shè)路333號（龍沙生物技術(shù)有限公司）GE生物園薪資：稅前7-9K，基本工資80% 績效20%，2個(gè)試用期，試用期工資不打折 職能類別：質(zhì)量管理/測試工程師(QA/QC工程師) 關(guān)鍵字：質(zhì)量質(zhì)量保證QA英文