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.
負責(zé)檢查生產(chǎn)清場、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.
負責(zé)現(xiàn)場質(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.
負責(zé)檢查和確認設(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.
負責(zé)不合格物料的檢查和監(jiān)控銷毀；
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)專業(yè)大專以上的學(xué)歷；
Languages語言: 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業(yè)英語水平，能很好的完成工作中涉及的這兩方面的工作。
Experience經(jīng)驗: 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；
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，并能嚴格的遵守GMP要求和執(zhí)行相關(guān)的SOP，對藥品生產(chǎn)和質(zhì)量管理中的一般問題能夠做出正確的判斷和處理；
聯(lián)系我時，請說是在云南招聘網(wǎng)上看到的，謝謝！