崗位職責(zé)
Responsible for the check in line clearance of production, material status, reprocessing, and packaging stages and other critical steps or aspects which may influence the quality of products.
負(fù)責(zé)檢查生產(chǎn)清場(chǎng)、物料狀態(tài)、返工、包裝和其他可能影響產(chǎn)品質(zhì)量的步驟;
Responsible for shop floor quality monitoring, sampling and relevant works, make sure all the products produced in Zhongshan site compliance with GMP.
負(fù)責(zé)現(xiàn)場(chǎng)質(zhì)量監(jiān)控、取樣和相關(guān)工作,確保所有中山工廠生產(chǎn)的產(chǎn)品符合GMP要求;
Responsible for the checking and qualifying of the equipment maintain, process and materials change.
負(fù)責(zé)檢查和確認(rèn)設(shè)備維修、工藝和物料的變更情況收集;
Responsible for the environmental monitoring and water system monitoring.
負(fù)責(zé)環(huán)境監(jiān)控和水系統(tǒng)監(jiān)控;
Responsible for checking on the disposal materials and monitor the destroying operation.
負(fù)責(zé)不合格物料的檢查和監(jiān)控銷(xiāo)毀;
Participate in any quality related issue investigation and evaluation.
參與質(zhì)量相關(guān)事件的調(diào)查和評(píng)估;
BPR collecting and first review.
批記錄的收集整理和初審。
任職要求
Education教育 : Graduate from pharmacy or relevant specialties above junior college.
必須是藥學(xué)或相關(guān)專(zhuān)業(yè)大專(zhuān)以上的學(xué)歷;
Languages語(yǔ)言: Mastering certain computer operating and professional English, and could finish task satisfactorily which refer to them.
具有一定的電腦操作水平和專(zhuān)業(yè)英語(yǔ)水平,能很好的完成工作中涉及的這兩方面的工作。
Experience經(jīng)驗(yàn): Obtained proper training on pharmaceutical quality management, and with more than one year’s relevant working experience.
有較好的藥品質(zhì)量管理培訓(xùn)和一年以上相關(guān)工作經(jīng)驗(yàn);
Familiar with items of GMP, can comply with requirements of GMP and relevant SOP strictly, and could judge and handle correctly common questions.
熟悉GMP條款,并能?chē)?yán)格的遵守GMP要求和執(zhí)行相關(guān)的SOP,對(duì)藥品生產(chǎn)和質(zhì)量管理中的一般問(wèn)題能夠做出正確的判斷和處理;
聯(lián)系我時(shí),請(qǐng)說(shuō)是在吉安人事人才網(wǎng)上看到的,謝謝!