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QA Ops与PCU经理
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33-52万 北京 本科 10年及以上 招聘 1 人 预计佣金 9K 08:40发布
72小时新发
JD基本信息
岗位职责
• Act as the QA PCU Lead to respond to operational QA business for PCU. 作为PCU质量保证团队的负责人负责相关的现场QA质量管理业务。 • Provide quality assurance oversight by performing routine walk-throughs and inspections on production, laboratory, warehouse, engineering deportment and other areas assigned where the business is responsible to ensure that all aspects of operations comply with cGMP legal and regulatory requirements as well as global guidelines 通过日常现场巡视及检查的方式对生产,实验室,库房,工程以及其它区域进行监督,保证所有相关操作符合cGMP、注册法规以及总部文件要求 • Ensure all batch records are reviewed, and when needs, ready for release as required, on behalf of site quality responsible. 确保批记录被审核,且需要时,可代表工厂质量负责人按照要求放行。 • Ensure that all manufacturing/packaging activities comply with the validated processes and the relevant sops and cGMPs 确保所有生产、包装活动符合工艺验证以及相关的SOP和GMP要求。 • Establish procedures and ensure continuous improvement of the PCU quality oversight and GMP documentation. 建立流程并持续改进关于PCU质量运营监督的设计和GMP相关的支持文件。 • Manage the PCU deviation and related customer complaint, corrective and preventative actions (CAPA), out of specification (OOS) handling, and monitor the CAPAs to prevent the recurrence of the not compliance incidents; demonstrate a high level of independent judgment and discretion in the timely identification, investigation and resolution of deviations potentially impacting the quality of products and processes; providing support and advice during cross functional investigations and when required, devise sampling procedures and directions for recording and reporting quality data. As quality representative, approve deviation and lab investigation, to ensure the process handling meet the requirement of regulatory and Sanofi procedure. 有效管理PCU偏差,纠正预防措施和OOS处理,并监控CAPA的落实以预防不符合事件的重现;需在工作中展现高度独立的、及时的判断决断能力;以及理清偏差对产品及工艺影响的能力; 如需要,在跨部门调查中提供支持和建议如提出取样方案,调查方向以及汇报相关质量数据。作为质量代表批准偏差及实验室调查,确保整个过程符合法规及总部要求。 • Support CAPA implementation and review CAPA effectiveness, approve the extension requests of CAPA in systems. 支持CAPA执行和回顾CAPA效果,作为质量代表批准系统中CAPA的延期请求。 • Ensure the plan in place. ensures all critical process parameters and quality attributes are monitored or analyzed. 确保监控和分析所有的关键工艺参数和关键质量特性。 • Support and participate project or improvement of products and product launch and technical study. Ensure a proper prioritization approach for high-level product assessments, product validation, compliance activities 支持和参与项目或产品的改善行动,产品转移和技术研究,对验证进行建议。确保产品质量风险评估、工艺验证和合规行动被优先考虑。 • Establish procedures and ensure continuous improvement of the operational quality oversight and GMP documentation. 建立流程并持续改进关于质量运营监督的设计和GMP相关的支持文件。 • Participate inspection, including the supplier inspection. 参与审计应对包括供应商审计。 • Establish and assure a continuous GMP training to APU to maintain a high level of GMP awareness. 建立并持续开展GMP培训以维护APU员工高水准的GMP意识。 • Act as the final evaluator of change quality to ensure changes are properly evaluated 作为变更质量最终评估人评估确保变更得到正确的评估。 • Develop people via training and coaching to enable them qualified for QA PCU work. Training curriculum up to dat. Ensure associates trained according to the training curriculum. 发展人员,使其能符合QA PCU工作要求。安装计划的要求实施培训,并保证培训及时更新。 • Perform people performance management. Make individual develop plan with personnel within team and build up technical ladder. 进行人员绩效管理。制定团队的个人发展计划,建立人才梯队。 • Approval of relevant documents on behalf of the QA Manager when the QA Manager is absent. 当QA经理缺席时代表QA经理批准相关文件 • Any other specific responsibility appointed by the senior management. 其他未尽职责,遵照上一级管理团队的要求执行。
任职要求
• Experience: 工作经验: with minimum 10 years’ experience in quality control and /or quality assurance, 3 years of which in management position. 至少5年QC或QA工作经验,3年以上管理经验。 • Soft skill: 通用技能: Problem solving and good communication良好的沟通及问题解决能力 • Technical skill: 专业技能: Must be a committed "quality" professional with knowledge of regulated quality systems within the pharmaceutical or related industry. 必须具备制药或相关行业的质量体系的“质量”专业知识经验。 • Education: 教育背景: At least a bachelor degree in pharmacy or chemistry or biology disciplines至少药学或化学或生物学或相关专业大学本科学历 • Languages: 语言要求: Good English verbal & written communications. 英语口语和书写熟练
所属行业:
生物技术/生物工程、制药
职能分类:
药品生产/质量管理
工作城市:
北京,招聘1人,详细地址:亦庄经济技术开发区兴盛街7号
职位要求
学历要求:
本科·统招·985/211
工作年限:
10年及以上
技能/证书:
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薪资福利
年薪范围:
33-52万*12薪
薪资福利:
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团队架构
所属部门:
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下属人数:
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职级职称:
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面试信息
面试轮次:
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视频面试:
不可以接受
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