招聘人数：1 人
性别要求：不限性别
Responsibilities: Ensure all the packing activities comply with the GMP requirementTo maintain / improve efficient product release procedure to ensure the product supply is maintained at a high quality standardLead, facilitate and support key business processes on behalf of QA in PETHas a direct involvement in regulatory inspectionsMaintain / Improve procedure, secure operation GMP complianceIdentify the quality and compliance gap and work out improvement plan with area managerLead and provide guidance in the daily job of the teamBuild and develop team and personnel capabilityOptimize performance outcomes of direct reports and ensure high quality IDP reviewIdentify and understand the SHE risk factors within the departmentDevelop and carry out plans to address the key SHE issues in the associated areas and ensure the follow up actions are carried out Requirements: Degree or equivalent professional qualification in a science/technical field such as Pharmacy, Biology, Chemistry8 years prior experience in GXP environment of pharmaceutical industry5 years prior experience in GMP manufacturing and quality management, including in process control or quality controlExperience of packing operation and process improvementExperience of working cross functionally across the supply chain with groups such as regulatory affairs, manufacturing, supply and account management, etcOverall quality management system and GMP knowledge Expert of quality management in packingExpert of quality risk managementKnowledge of up-to-date technology and regulatory trendExperience of internal and external audit managementGood collaboration, team coaching and people development capabilityGood command of English
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