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Senior Specialist II Quality Assurance
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Manufacturing Transport Logistics
💰 Salary Not shared
📊 Market 20,000 GBP–35,000 GBP/mo (240,000 GBP–420,000 GBP/yr)
About the Company
Typical Accountabilities 主要职责 Definition of Responsibilities 职责界定 Understand/interpretation of principal to drive improvement of process 理解/解释相应的原则以推动过程改进 Issue/risk identified 问题/风险识别 Solve the problem and drive the improvement across function 解决问题并推动跨职能部门改进 Make quality decision - Quality review, approval, release 做出质量决定-质量审核 批准 放行 BPC (Business process champion) role 业务流程负责人角色 SME(Subject Matter Expert) 特定领域专家 Team management 团队管理 Coach and mentor 培训及指导 Management of QA affairs QA 日常业务的处理 1. Shop Floor quality management 生产一线质量管理 Identify the quality risk during daily work, improve continuously. 识别日常工作中的质量风险点 持续改善 Critical shop floor issue handling and decision 生产一线严重事件的现场处理及决策 2. Quality issues handling 质量事件处理 Qualified investigator to lead Major/Critical quality issue handling, investigation and assessment 作为有资质的调查员 主导重大/严重质量事件的处理 调查和评估 Minor deviation approval 负责微小偏差的批准 3. Product releaser 产品放行 4. Business support and continuous improvement 业务支持及持续改善 Support PET business processes regarding compliance and quality 就法规符合性和质量给予PET 业务支持 Drive continuous improvement in cross function 推动跨部门的持续改善 Lead team project/support cross team project 负责团队项目/支持跨团队项目 5. Inspections and audit 自检及审计 To be involved in regulatory inspections and self-inspection 参与审计和自检 Act as coordinator in regulatory or global audit if needed. 在审计过程中担当协调员(如需要) 6. Perform and deliver quality activities assigned. 执行其他安排的质量活动 Quality systems management 质量体系管理 1. Draft,
Requirements
- ● University graduate, major in pharmaceutical or related subjects
- ● 大学毕业 药学或相关学科
- ● years of QA or production working experience
- ● 年以上QA 或生产工作经验
- ● years of QA working experience
- ● Have multiple national enterprise working experience
- ● Cross Function working experience
- ● Capabilities
- ● Solid GMP and quality system management knowledge 良好的GMP 和质量体系管理知识
- ● Familiar with up-to-date technology and regulatory trend 熟悉行业技术和法规
- ● Familiar with quality risk management 熟悉质量风险管理专家
- ● Knowledge of process control methodology and statistics, for example Cpk, FMEA 具备过程控制方法和统计学的知识 类似Cpk,FEMA 等工具
- ● Working knowledge of Microsoft applications, SAP or similar system 熟悉微
- ● 软应用 SAP 或类似系统
- ● Good English 英语水平良好
- ● Good Computer skill 电脑使用熟练
- ● Good communication skills, proactive leadership, strong quality minds and strong service minds 良好的沟通技巧 主动的领导意识 强烈
- ● Date Posted 29-Sep-2026
- ● Closing Date 30-Oct-2026
- ● AstraZeneca embraces diversity and equality of opportunity. We are committed to building an inclusive and diverse team representing all backgrounds, with as wide a range of perspectives as possible, and harnessing industry-leading skills. We believe that the more inclusive we are, the better our work will be. We welcome and consider applications to join our team from all qualified candidates, regardless of their characteristics. We comply with all applicable laws and regulations on non-discrimination in employment (and recruitment), as well as work authorization and employment eligibility verification requirements.
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