產(chǎn)品檢測技術(shù)崗位職責(zé)
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.