日韩第一精品,五月天丁香亚洲,欲望之翼中文字幕电影完整版未删减百度云,沉默的冰山电影完整版在线观看,2024久久精品,俺来俺去www,黑人性hd

驗(yàn)證經(jīng)理崗位職責(zé)：

提供藥品生產(chǎn)驗(yàn)證咨詢（廠房/設(shè)施/設(shè)備/工藝等）；
Consulting for Pharmaceutical plant Validation(Premises/facility/equipment/process etc)

負(fù)責(zé)組織藥廠驗(yàn)證活動(dòng)的計(jì)劃和實(shí)施（包括建造期間的IO/PQ確認(rèn)活動(dòng)和生產(chǎn)期間的驗(yàn)證活動(dòng)）
Responsible for validation consulting planning and execution (including IO/PQ and process validation)

參與驗(yàn)證咨詢和服務(wù)銷售支持活動(dòng)
Participating validation consulting and service sales support.

負(fù)責(zé)根據(jù)客戶產(chǎn)品和工藝編制/審核驗(yàn)證咨詢文件、培訓(xùn)和指導(dǎo)客戶驗(yàn)證活動(dòng)實(shí)施；
Preparing/Review validation consulting documents; training and directing client implementation.



專業(yè)技能及經(jīng)驗(yàn)要求

JOB KNOWLEDGE SKILLS AND EXPERIENCE

8年以上藥廠或制藥工程驗(yàn)證或QA工作經(jīng)驗(yàn)
Over eight years work experience include validation or QA in Pharmaceutical plants or Pharmaceutical Engineering fields

熟悉藥品生產(chǎn)驗(yàn)證相關(guān)法規(guī)和指南（EU, USA, WHO, PIC/S, ISPE and ICH）
Familiar with the relevant regulations/guidelines of the pharmaceutical manufacturing practice and validation of EU, USA, WHO, PIC/S, ISPE and ICH.

本科以上學(xué)歷


At least bachelor degree majoring in Pharmaceutical or Engineering.

英語(yǔ)熟練
Good English Skills

能經(jīng)常出差
Business trip in China is preferred.