pWe'rerecruitingforanexcitingopportunitywithanaward-winningPharmaceuticalorganizationinCork.Thispositionisexcellentforthosewhowanttojoinaleadingmultinational./ppDuties:/pulliExecutecycledevelopment,cleaningvalidation,andequipmentPQ./liliWriteandadheretovalidationstrategies,coordinatewithoutsidevendors,writeprotocols,submitsamples,analyzeresults,andpreparetechnicalreports./liliExecutebusinessactivitiessuchasequipmentperiodicreviews,cleaningperiodicreviews,CAPAs,deviations,changecontrol,riskassessments./liliSupportcommissioningphasebyreviewingandapprovingdocuments.Ensuredocumentationcomplieswithstandards./liliParticipateincross-functionalproblem-solvingteamsfortroubleshootingandinvestigations./liliWritetechnicalreportsandanalyzedatastatistically./liliAdheretothelatestregulatoryguidelines./liliRepresenttheIPToncross-functionalprojectteams./liliProvidetechnicalinputandpresentasanSMEonrelevanttopics./liliEnsurecompliancewithsiteEHSpolicy,cGMP,andotherbusinessregulations./liliParticipateinManufacturingDivisionQualityManagementSystem(QMS)requirements./li/ulpRequirements:/pulliExperienceasavalidationspecialistinapharmaceuticalorregulatedenvironmentandaB.Sc.Degreeorrelatedqualification./liliExperienceinC&Qvalidation,cleaningvalidation,equipmentvalidation,processoperations,ormanufacturing./liliWorkingknowledgeofGxPsystemssuchasGLIMSandeVAL./li/ulpPleasecontactSeánMcCarthyforfurtherinformation./p