制藥行業(yè)崗位職責(zé)3篇

Word———制藥行業(yè)崗位職責(zé)3篇【第1篇】制藥行業(yè)銷售崗位職責(zé)

制藥行業(yè)銷售工程師寶帝流體掌握系統(tǒng)寶帝流體掌握系統(tǒng)(上海)有限公司,寶帝,寶帝流體掌握系統(tǒng),流體掌握系統(tǒng),寶帝職責(zé)描述:

1、負(fù)責(zé)氣動(dòng)過程閥門,工業(yè)用傳感器類的產(chǎn)品推廣

2、負(fù)責(zé)銷售工作整體運(yùn)作的有效執(zhí)行,完成公司業(yè)績和達(dá)成預(yù)期市場占有率目標(biāo)

3、開發(fā)區(qū)域內(nèi)及制藥行業(yè)內(nèi)新客戶

4、維護(hù),鞏固,提升與老客戶的關(guān)系

5、熟識(shí)行業(yè)動(dòng)態(tài),供應(yīng)行業(yè)趨勢分析,為客戶供應(yīng)技術(shù)支持,并擅長發(fā)覺新商機(jī)

任職要求:

1、本科(全日制)及以上;

2、機(jī)械、機(jī)電、機(jī)械自動(dòng)化、電氣自動(dòng)化、儀表自動(dòng)化、化工工程工藝、制藥工程工藝、發(fā)酵等相關(guān)專業(yè)優(yōu)先;

3、3年以上閥門、儀表等相關(guān)產(chǎn)品的銷售閱歷,制藥行業(yè)的工程公司、設(shè)備成套商、衛(wèi)生管道相關(guān)工作閱歷;

4、制藥行業(yè),尤其是生物制藥、疫苗、血液制品德業(yè)銷售閱歷優(yōu)先。

【第2篇】生物制藥行業(yè)崗位職責(zé)

技術(shù)支持工程師(生物制藥行業(yè))安諾杭州安諾過濾器材有限公司,安諾,安諾崗位職責(zé):

1、負(fù)責(zé)與客戶的技術(shù)溝通工作,收集客戶的技術(shù)要求,并進(jìn)行初步分析和分解;

2、負(fù)責(zé)產(chǎn)品應(yīng)用背景評估和技術(shù)分析,依據(jù)客戶需求和產(chǎn)品性能供應(yīng)合適的解決方案;

3、負(fù)責(zé)本行業(yè)過濾技術(shù)應(yīng)用前景及市場分析,使產(chǎn)品開發(fā)落地;

4、負(fù)責(zé)解答客戶對產(chǎn)品使用、投訴等相關(guān)問題;

5、負(fù)責(zé)本行業(yè)的內(nèi)、外技術(shù)溝通和培訓(xùn)。

任職要求:

1、生物化工、生物制藥相關(guān)專業(yè)碩士及以上學(xué)歷。

2、具有優(yōu)秀的溝通表達(dá)力量及組織協(xié)調(diào)力量。

3、熟識(shí)原料藥、無菌制劑等產(chǎn)品制造工藝。

4、能協(xié)作公司適應(yīng)短期出差。

【第3篇】制藥行業(yè)崗位職責(zé)

qamanager-制藥行業(yè)responsibilities:

inchargesitequalitycontrol,qualitysystemmanagement.

setupthecompanyqualitygoalandregularlyreviewthestatusofqualitytarget.trainandguidetheteamtoreachfunctionalqualitygoal.

manageengineersandinspectorsteamofqasection,coordinatewithotherdept./team.

definethequalityassurancepolicyandprocess,leadtheimplementationofqualityassurancemodelsandsystemthatcanguaranteetotheorganizationcustomersatisfaction,continuousimprovementandorganizationaleffectivenessinordertoachievemaximumcompetitiveness.

prepareweeklyandmonthlyqualityreports,makecontinuousqualityimprovementthroughgoodteamwork

connectcustomerneedswiththeconditionsoftheproductionprocessanddefineproductguidelinesandcriteriaandtheconditionsofthemanufacturingprocess.

qualitymanagementsystemimplement,monitorandmaintain.conductregularinternalqualityauditstoensureitseffectivenessandsuitability.

ensurethatthequalitymanagementsystem(qms)iseffectivelyestablished,implementedandmaintainedtobeincompliancewithiso9001,iso13485,21cfr820,cestandardsandchinesegmp.

manageallinspectioninstrument,inspectiongages,andtestfixtures/tooling/equipment.

requirement:

10+qualitymanagementexperience,5+sitequalitycontrolexperienceinpharmaceutical,ivdormedicaldeviceindustry

peoplemanagementexperience

experiencediniso13485,21cfr820,gmp,qsr

fdainspectionexperience

soundknowledgeinprocessqualitycontrolandriskmanagement

stronginleadership

goodatcommunication,coordination

fluentinenglish

responsibilities:

inchargesitequalitycontrol,qualitysystemmanagement.

setupthecompanyqualitygoalandregularlyreviewthestatusofqualitytarget.trainandguidetheteamtoreachfunctionalqualitygoal.

manageengineersandinspectorsteamofqasection,coordinatewithotherdept./team.

definethequalityassurancepolicyandprocess,leadtheimplementationofqualityassurancemodelsandsystemthatcanguaranteetotheorganizationcustomersatisfaction,continuousimprovementandorganizationaleffectivenessinordertoachievemaximumcompetitiveness.

prepareweeklyandmonthlyqualityreports,makecontinuousqualityimprovementthroughgoodteamwork

connectcustomerneedswiththeconditionsoftheproductionprocessanddefineproductguidelinesandcriteriaandtheconditionsofthemanufacturingprocess.

qualitymanagementsystemimplement,monitorandmaintain.conductregularinternalqualityauditstoensureitseffectivenessandsuitability.

ensurethatthequalitymanagementsystem(qms)iseffectivelyestablished,implementedandmaintainedtobeincompliancewithiso9001,iso13485,21cfr820,cestandardsandchinesegmp.

manageallinspectioninstrument,inspectiongages,andtestfixtures/tooling/equipment.

requirement:

10+qualitymanagementexperience,5+sitequalitycontrolexperienceinpharmaceutical,ivdormedicaldeviceindustry

peoplemanagementexperience

experiencediniso13485,21cfr820,g