
Medical Technologist-Flow 流式檢測(cè)技術(shù)員

職位描述
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.
Expericences
Flowbackgroundispreferred.
企業(yè)簡(jiǎn)介
科文斯,全球性的合同研究組織(CRO)Covance Inc.是全球服務(wù)最全面的藥物研發(fā)公司。
我們致力于推動(dòng)醫(yī)療保健事業(yè)發(fā)展并實(shí)現(xiàn)Solutions Made Real?,通過(guò)向制藥公司和生物科技公司提供高質(zhì)量的非臨床、臨床前試驗(yàn)、臨床和商業(yè)化服務(wù),幫助減少藥物研發(fā)的時(shí)間和成本。憑借豐富的經(jīng)驗(yàn)與深厚知識(shí),我們具備獨(dú)特的優(yōu)勢(shì),能為客戶合作伙伴提供不僅僅局限于測(cè)試的獨(dú)到見(jiàn)解。
我們還向化學(xué)品、農(nóng)用化學(xué)品和食品行業(yè)提供實(shí)驗(yàn)室測(cè)試服務(wù),同時(shí)也是毒理學(xué)分析服務(wù)、中心實(shí)驗(yàn)室服務(wù)、藥物篩選服務(wù)的市場(chǎng)領(lǐng)導(dǎo)者,以及III期臨床試驗(yàn)管理服務(wù)的全球頂級(jí)提供商。
科文斯官網(wǎng): https://www.covance.com/
職位發(fā)布企業(yè)

科文斯醫(yī)藥研發(fā)(北京)有限公司上海分公司
企業(yè)性質(zhì):外資企業(yè)
企業(yè)規(guī)模:5000-10000人
成立年份:2006
企業(yè)網(wǎng)址:www.covance.com
企業(yè)地址:上海市普陀區(qū)嵐皋路555號(hào)602-606室
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職位發(fā)布日期: 2019-04-25