職位描述
崗位工作地點在青島，項目建設(shè)期間參與項目前期的設(shè)計，建造，調(diào)試和確認等工作，作為用戶代表更好的支持項目組實現(xiàn)青島pMDI工廠的建設(shè)。通過精益標準化和專業(yè)技能持續(xù)標準化與改善如SOP/工作指導(dǎo)以確保項目期間的知識，技能和經(jīng)驗?zāi)軌騻鞒幸灾С治磥淼纳虡I(yè)化生產(chǎn)，并在項目早期就注重工藝/設(shè)備/操作等的持續(xù)改善工作。加強和內(nèi)外部利益相關(guān)方的溝通。This role is based in Qingdao, During project phase involved in project Design、Construction、Commissioning and Qualification as end user to support Global engineering team/Project team to deliver Qingdao pMDI project. And standardize knowledge and experience during project and startup phase to prepare for Qingdao site PQ and PV and ensure following BAU smoothly in terms of daily operation including SOP/WI ready and continuously improve process/equipment/operation from project to BAU transition. have good communication internally and externally.進入商業(yè)化生產(chǎn)期間負責持續(xù)不斷提高生產(chǎn)團隊的KPI指標，促進團隊人員的技術(shù)能力不斷提高，就生產(chǎn)、質(zhì)量、安全、設(shè)備方面的問題與內(nèi)部和外部客戶建立高效的溝通。培訓(xùn)和監(jiān)督團隊成員的個人工作行為符合相應(yīng)SOP和AZ標準。Moving into BAU responsible for continuous improve product team KPI and facilitate team member capability constant improvement, communicate with external and internal customer and supplier on production, quality , SHE, machine issue .This role will train and lead other product people behavior to compliance with SOP ,and AZ standard.負責生產(chǎn)流程運作，規(guī)定生產(chǎn)流程和操作標準。按照安全，質(zhì)量，效率和成本的要求，負責規(guī)定流程的日常運行。Responsible for the Product Process Operation, to defined process and operational standards. They carry responsibility for the day-to-day performance of defined processes in terms of adherence to Safety, Quality, Efficiency and Cost.負責PET層面的項目執(zhí)行以支持生產(chǎn)的持續(xù)改進。支持PET負責人在生產(chǎn)策略執(zhí)行和業(yè)務(wù)發(fā)展和優(yōu)化，人員發(fā)展和精益執(zhí)行。Responsible for initiatives/project management in PET level for continuous improvement from BAU perspective and support PET leader on wider strategy deployment 、business development and optimization , people development and lean implementation.Specific Responsibilities/Tasks? 參與到項目的不同階段，作為最終用戶提供有價值和專業(yè)的建議到項目建設(shè)中Fully involved in different project phase and have valuable input as end user? 學(xué)習(xí)并運用其他工廠和行業(yè)的經(jīng)驗實踐到新工廠Learn and apply best practice from other sites and other experiences to Qingdao project? 端到端的思維持續(xù)標準化和持續(xù)改善的理念和能力，通過項目期間的參與，實踐為未來的商業(yè)化生產(chǎn)的垂直啟動和成功做好充足的準備End to end mindset to be involved in project and ensure standardization and continuous improvement to BAU vertical startup through expertise, lean and experience gained from project phase? 利益相關(guān)方之間良好的內(nèi)外部溝通Good communication with stakeholder both internally and externally? 將精益和TPM和先進的維修理念運用到項目執(zhí)行和后續(xù)的商業(yè)化生產(chǎn)Embed lean/TPM/Advanced maintenance system during project phase to BAU? 持續(xù)標準化，文件化數(shù)字化相關(guān)項目期間的工作經(jīng)驗并能指導(dǎo)和運用到BAU的實踐中Documentation and standardization activities during project and BAU phase? 良好的協(xié)調(diào)溝通調(diào)度能力，確保項目C&Q,PQ/PV的成功Strong coordination, communication, and scheduling skills capability to ensure C&Q, PQ/PV successfully日常生產(chǎn)管理Day-to-day production management? 管理所負責工段生產(chǎn)事宜，保證生產(chǎn)符合GMP和公司標準的要求Supervise all production activity meet the requirement of GMP and company standards.? 安排生產(chǎn)保證生產(chǎn)計劃完成Schedule detail production activity to ensure the production plan was fulfilled.? 調(diào)查和矯正生產(chǎn)過程偏差I(lǐng)nvestigate and rectify deviation during granulation.? 優(yōu)化生產(chǎn)流程，保證生產(chǎn)效率和結(jié)果Optimize process to keep production efficiency and result? 復(fù)核和釋放生產(chǎn)記錄文件Check and release the BPR? 頒發(fā)維護SOP，確保標準化生產(chǎn)Issue and update the relative SOPs to supervise the production activity? 監(jiān)督文件記錄及管理Supervise production document management GMP 要求GMP requirements? 理解業(yè)務(wù)活動中涉及GMP的相關(guān)內(nèi)容及可能對產(chǎn)品質(zhì)量產(chǎn)生的影響Understand the impacts of daily work on GMP requirements and product quality? 參加GMP相關(guān)培訓(xùn)，確保業(yè)務(wù)活動持續(xù)符合GMP要求Attend GMP trainings and ensure that daily work is compliant to GMP consistently? 嚴格執(zhí)行本崗位的GMP相關(guān)規(guī)程Strictly follow GMP SOPs.? 向直線經(jīng)理或QA溝通工作中遇到的GMP相關(guān)問題 Report to line manager or QA about GMP questions encountered in daily work
