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環(huán)境檢測(cè)技術(shù)經(jīng)理崗位職責(zé)任職要求

2024-07-29 閱讀 3383

環(huán)境檢測(cè)技術(shù)經(jīng)理崗位職責(zé)

崗位職責(zé):

1.負(fù)責(zé)或參與環(huán)境領(lǐng)域的咨詢業(yè)務(wù)相關(guān)工作,如VOCs綜合治理、環(huán)境質(zhì)量評(píng)估、場(chǎng)地調(diào)查、污染場(chǎng)地修復(fù)等,包括方案編制、咨詢項(xiàng)目的全過(guò)程執(zhí)行等;

2.負(fù)責(zé)跟蹤/更新所負(fù)責(zé)領(lǐng)域的環(huán)保政策、法規(guī)以及技術(shù)動(dòng)態(tài),完成定期信息通告與宣傳;

3.協(xié)助維護(hù)或開發(fā)環(huán)境監(jiān)測(cè)相關(guān)項(xiàng)目的客戶;

4.負(fù)責(zé)團(tuán)隊(duì)內(nèi)以及前線的相關(guān)培訓(xùn);

5.提供負(fù)責(zé)領(lǐng)域的技術(shù)性支持工作;

6.參與團(tuán)隊(duì)以及項(xiàng)目管理過(guò)程中流程規(guī)范工作,如體系文件、項(xiàng)目流程管理文件編制等。

任職要求:

1、環(huán)境工程、化工等相關(guān)專業(yè)大學(xué)本科以上學(xué)歷,五年以上工作經(jīng)驗(yàn),環(huán)境監(jiān)測(cè)或檢測(cè)等相關(guān)背景,有化學(xué)實(shí)驗(yàn)室建設(shè)經(jīng)驗(yàn)或中級(jí)工程師職稱優(yōu)先。

2、了解環(huán)境監(jiān)測(cè)的國(guó)家政策、行業(yè)狀況及發(fā)展趨勢(shì),了解國(guó)內(nèi)外環(huán)境監(jiān)測(cè)的發(fā)展?fàn)顩r,深入掌握環(huán)境監(jiān)測(cè)的應(yīng)用范圍、常規(guī)技術(shù)手段和前沿技術(shù)。

3、熟悉環(huán)境領(lǐng)域工程咨詢類業(yè)務(wù),有廢氣治理咨詢或土壤場(chǎng)地調(diào)查等項(xiàng)目經(jīng)驗(yàn)。

4、獨(dú)立開拓市場(chǎng)、組建及管理部門的能力及相關(guān)經(jīng)驗(yàn),豐富的業(yè)務(wù)相關(guān)各層級(jí)資源,具備一定的財(cái)務(wù)知識(shí)。

5、大局觀和綜合分析能力,強(qiáng)烈的進(jìn)取心、成就欲望和良好的職業(yè)操守,抗壓能力強(qiáng),工作具有良好的計(jì)劃性和目標(biāo)性,具備良好的策劃、組織、公關(guān)能力,擅于解決問(wèn)題。

環(huán)境檢測(cè)技術(shù)經(jīng)理崗位

篇2:實(shí)驗(yàn)室檢測(cè)技術(shù)員崗位職責(zé)實(shí)驗(yàn)室檢測(cè)技術(shù)員職責(zé)任職要求

實(shí)驗(yàn)室檢測(cè)技術(shù)員崗位職責(zé)

崗位職責(zé):

1.從事熒光定量PCR、一代/二代測(cè)序等實(shí)驗(yàn)基本操作及數(shù)據(jù)分析等工作;

2.及時(shí)處理臨床和市場(chǎng)部反饋的信息;

3.撰寫SOP等文件和報(bào)告;

4.按照實(shí)驗(yàn)室的質(zhì)量控制要求,填寫相關(guān)記錄表單,維護(hù)實(shí)驗(yàn)儀器,保持實(shí)驗(yàn)技術(shù)平臺(tái)的正常運(yùn)轉(zhuǎn)。

任職資格:

1、分子生物學(xué)、醫(yī)學(xué)檢驗(yàn)相關(guān)專業(yè)本科及以上學(xué)歷;

2、具有分子檢測(cè)技術(shù)平臺(tái)(PCR、測(cè)序、FISH等)經(jīng)驗(yàn)者優(yōu)先考慮;

3、有檢驗(yàn)師資格證者或PCR上崗證者優(yōu)先考慮;

4、誠(chéng)實(shí)正直,工作認(rèn)真嚴(yán)謹(jǐn),具有良好的團(tuán)隊(duì)合作精神,具有高度的責(zé)任感和敬業(yè)精神。

篇3:基因檢測(cè)技術(shù)員崗位職責(zé)基因檢測(cè)技術(shù)員職責(zé)任職要求

基因檢測(cè)技術(shù)員崗位職責(zé)

MedicalTechnologist-Genomics基因檢測(cè)技術(shù)員科文斯醫(yī)藥研發(fā)科文斯醫(yī)藥研發(fā)(北京)有限公司上海分公司,科文斯Responsibilities/Duties:

?Performassignedclinicallaboratorytestingaccuratelyandinatimelymanner.

oResolvependings.Retrieveandcheckspecimensagainstpendinglist.Documentspecimendiscrepancies.Notifylaboratorymanagementwhenspecimendiscrepanciesarenotresolved.

oPrepareworkstationandinstrumentationfortheassignedtesting.oProperlyhandlespecimensandindependentlyresolvetechnicalspecimenissuesinpreparationforanalysisandspecimenstorage.Contactinternalcustomersforclarificationasneeded.

oOperateinstrumentstoperformtestinginaccordancewithestablishedwrittenprocedures.

oPerformsroutinetestingandcalculationsasrequired.

oResolveroutineandnon-routineassayproblems.

?Ensurethevalidityoftestsresultsthroughtheperformanceofestablishedqualityassuranceandqualitycontrolprocedures.

oPerformexperiments,asscheduled,forevaluationofnewCalibratorand/orQClots.Summarizeresultsofinvestigationsandcompiledataforreviewbymanagement.

oDocumentqualitycontrolresults.InterpretqualitycontrolresultsaccordingtoWestgardrulesorotherestablisheddepartmentalproceduresandaccuratelydocumentbiases,warningsandviolationsofcontrolvalues.

oDocumentcorrectiveactionforunusualoccurrences(e.g.QCviolations,instrumentrelatedproblems).

oAnalyzeproficiencytestingsurveysamplesaspatientspecimens.?Reagents/Materials/Supplies:

oReceive,openandplaceinserviceallreagents/materialsaccordingtoSOPs.

oPrepareandproperlylabelreagent,qualitycontrol,calibratormaterial.

oDocumentimplementationofnewreagents/materialsaccordingtoSOPs.

oPerformparalleltesting,linearity’s,stability,otherqualitycontrolpracticesneededtoensurevalidityofmaterialpriortobeingplacedintoservice.

oPerforminventorycontrolofsuppliesandreagentsasapprovedbymanagement.

?ResultEntry(Auto-verificationandmanualentry).

oWhendataismanuallyentered(e.g.QC,patientdata)ensurepeerreviewisperformedanddocumentedpriortoreleaseofresults.

oPrepareproperdocumentationoftestresultsandenterintotheinformationsystem.

oGenerateanappropriateaudittrailforallactivities.

oDocumentandcommunicateanyresultreportingproblemsorinconsistenciestolaboratorymanagement.

oCompletetestingwithintheexpectedturnaroundtimetomeetcustomers’expectations.

?EnsuresmaintenanceofinstrumentsandequipmentisperformedaccordingtomanufacturerandSOPrequirements,anddocumentedaccordingtoSOP.oCalibrateinstruments,equipmentand/orassaysasrequiredanddocument.

oPerformbasicinstrumentandequipmenttroubleshooting.

oPerformpipettecalibrationsanddocumentaccordingtoSOP.

oNotifylaboratorymanagementwhenaninstrumentorequipmentdoesnotmeetspecifications.

?ComplywithregulatoryguidelinesandCovanceStandardOperatingProcedures(SOPs)atalltimes.

?Training

oIndividualisresponsibleformaintaininghis/hercompleteup-to-datetrainingfileandisaccountableforcorrectinganddeficienciesfoundinhis/hertrainingfile.

oIndividualisresponsibleforensuringhe/sheistrainedandtrainingisdocumentedpriortoperformingatask.

oTheindividualsuccessfullycompletes,asscheduled,competencyassessmentandensurescompetencytestingdocumentationisprovidedtomanagementforreview/retention.

oCompetentlyperformsdepartmentdutiesassetforthinthedepartmenttrainingchecklist(s).

oMayassistintrainingnewemployeesandfollows-uptoensuretrainingisunderstood.

oAttends,asscheduled,department,mandatoryandothermeetingsandtraining,asrequiredaccordingtotrainingmatrices.

?Worktoachievepartnershipwithbothinternalcustomersandexternalclientsby:

oPulldatainatimelymannerforreviewbyQAandexternalclients.

oContributetotheprovisionofaccurateverbalorwrittenresponsetointernalQAandclientauditfindings.Coordinate,whereneeded,withotherresourcestoresolveissue.

oResearchesandpreparesaresponsefollowinginvestigationforqualitypurposes.Coordinate,whereneeded,withotherresourcestoresolveissue.

oResearchandrespondsinatimelymannertointernalcustomerinquiriesregardingstatusoftestresults,retrievalofsamplesfortesting/storageandotherneeds.

oUnderstanddepartmentmetricsandgoals.

?Demonstrateproficiencyinapplicablecomputersystemsandsoftware.

?AdherestoestablishedSafetypoliciesandUniversalprecautionguidelinesatalltimes.Maintainsaclean,organizedandsafeworkenvironment.Minimizesbiohazardwaste.Cleansworkstationandmaterialsdaily.

?Takesactionforthedepartmentwhenadditionalresponsibilitiesandopportunitiesarepresented.

?Providelaboratorymanagementwithareportofactivitiesuponrequest.

?Otherdutiesasassigned.

Education/Qualifications

Required:

?IndividualmustqualifyastestingpersonnelunderMoHregulations.

Preferred:

?Bachelor'sdegreeinMedicalTechnologyorcompletionofatleasta12-monthtrainingprograminMedicalTechnology.

OR

?Bachelor'sdegreeinachemical,physicalorbiologicalsciencefromanaccreditedcollegeoruniversityandoneyeartrainingand/orexperienceinthespecialtyinwhichtestingistobeperformed.SuchtrainingmustbeequivalenttothatreceivedinaschoolofMedicalTechnology.

Experience

1yearlabexperience,chemistrydepartmentprefer.