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產(chǎn)品檢測技術(shù)崗位職責(zé)

2024-07-28 閱讀 6212

技術(shù)服務(wù)工程師-標簽檢測產(chǎn)品部大恒圖像視覺北京大恒圖像視覺有限公司,大恒圖像,大恒圖像視覺,大恒職責(zé)描述:

1、負責(zé)客戶項目的現(xiàn)場實施。

2、為客戶提供產(chǎn)品相關(guān)的計術(shù)咨詢、售后服務(wù)維修。

3、配合區(qū)域銷售完成產(chǎn)品測試。

任職要求:

1.有強烈的責(zé)任心、事業(yè)心,進取心、勤奮踏實,能夠在壓力下獨立工作;

2.計算機相關(guān)專業(yè)、熟悉windows操作系統(tǒng);具有英語口語表達溝通能力。

3.較強的學(xué)習(xí)能力,良好的語言表達與溝通能力,具有一定的故障分析能力。

4.具備團隊合作精神,能適應(yīng)經(jīng)常性出差。

篇2:實驗室檢測技術(shù)員崗位職責(zé)實驗室檢測技術(shù)員職責(zé)任職要求

實驗室檢測技術(shù)員崗位職責(zé)

崗位職責(zé):

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

2.及時處理臨床和市場部反饋的信息;

3.撰寫SOP等文件和報告;

4.按照實驗室的質(zhì)量控制要求,填寫相關(guān)記錄表單,維護實驗儀器,保持實驗技術(shù)平臺的正常運轉(zhuǎn)。

任職資格:

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

2、具有分子檢測技術(shù)平臺(PCR、測序、FISH等)經(jīng)驗者優(yōu)先考慮;

3、有檢驗師資格證者或PCR上崗證者優(yōu)先考慮;

4、誠實正直,工作認真嚴謹,具有良好的團隊合作精神,具有高度的責(zé)任感和敬業(yè)精神。

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

基因檢測技術(shù)員崗位職責(zé)

MedicalTechnologist-Genomics基因檢測技術(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.