Education/Training:? BachelordegreeWorkExperience:? Minimum3yearsrelevantexperienceRequiredpre-requisitesskills/experience:? WorkingknowledgeforGMPcrequirements,ISO9001qualitysystems.
? Workingexperienceinpharmaceuticalindustryand/orcosmeticsindustrywithMultinationalCompanies(MNCs)ispreferred? Knowledgeofprocesscontrol&
capabilitymethodology,forexampleCpk,FMEA.
? Knowledgeofqualityinvestigation? GoodinEnglish? GoodMSOfficeSkills? GoodcoordinationandcommunicationDutiesandResponsibilities? CreateandMaintaintheQualityDocumentSystemProcedureaccordingtoGMPc,corporatepolices,regulatoryrequirementthroughthecoordinationofotherfunctions.
? OrganizeandimplementtheeffectivemanagementofqualityfilessuchasSOPs,specification,eBRtoensurethevalidversionsareusedintherighttimeandtherightplace.
? CarryroutineQAactivities,include:a) Deviation,CAPAmanagementb) Changerequestevaluationandfollowupc) Takepartininternalauditd) Complianthandlinge) Batchrecordreviewingf) In-processcontrolg) Investigationforqualityissuesh) Dailycoordinationwithallfunctionsregardingcomplianceandquality? SupportforHRforGMPtraining? EnsureSHEmanagementinhis/herownworkingarea
职位详细信息
工作性质：全职
工作地点：江苏-泰州
学历要求：本科
性别要求：性别不限
薪水待遇：面议
岗位描述