OPPO质量经理
任职要求
1.本科及以上学历，通信、电子、机械等工科类相关专业；
2.掌握质量管理方法及工具，具有手机产品质量管理或项目管理经验者优先；
3.熟悉新产品开发流程（IPD流程），对流程审计、优化知识有一定的了解；
4.具有跨部门协调沟通的能力，具有团队精神，性格稳重、扎实，有快速吸纳新知识的能力工作职责
1.负责手机研发项目的质量策划，组织团队制定项目质量目标、品质改善管控计划，并监控实施； 2.负责研发项目三新风险识别，在关键节点进行质量风险控制及评估，并不断优化； 3.在项目不同阶段，组织项目团队进行技术成熟度评审及验收，及时分析与改善不达标问题，持续改进； 4.产品上市质量达成情况的跟踪及问题的推动解决； 5.负责产品研发过程中IPD流程的引导、审计； 6.有品牌手机ODM工作经验者优先。
1.全面负责公司质量管理工作，策划、建立和维护公司的质量管理体系（包括设计和生产），组织制定产品标准和质量控制方案； 2.组织制定公司质量目标，分解目标，并监督、指导各部门制定和达成质量目标； 3.负责公司设计开发、生产过程的质量监督和管理； 4.负责供应商研发过程及制造过程的质量监督和管理； 5.负责质量体系内部审核和监督； 6.负责质量问题的分析和处理。
Position: QM (Quality Manager) Department: DI PA CNP What are my responsibilities? · Product Quality Management: o Establish, implement and maintain the comprehensive product R&D quality management system with alignment with Headquarters (Siemens global R&D / PLM quality standard) o Lead the product and process audits to ensure compliance with standards/guidelines o Manage product/process change to ensure product quality o Conduct the failure analysis and risk assessment for the product. And implement preventive/corrective actions o Analysis and follow up to fast response to customer complaints on product quality · Project Quality Management: o Define the project quality plan based on the specific requirements of the project o Project specific process tailoring (if needed) together with project/product manager o Milestone Check: § Prepare and perform the milestone readiness check (Quality Gate) with project/product manager and the project core team § Signoff the quality related documents o Track/analysis on the project quality metrics/KPI and generate project quality report o Drive continuous improvement initiatives on project quality · Supplier Quality Management: o Qualify and evaluate the supplier quality performance o Conduct supplier audit and assessment on their quality system and process o Help supplier understand the Siemens Quality requirements and drive supplier quality development program o Monitor supplier delivery and quality metrics · Process Definition & Optimization: o Align with BU Headquarters to define/optimize the quality management process (including gate-stage, waterfall, agile etc.) which fits to the local product development. o Define the quality related process for both internal development products and ODM products o Define the templates, instructions and best practices for the documents to be used in the product lifecycle management process o Provide the process, quality awareness and EHS training to employees o Continuous optimization on the process to fit on the actual project/product situation and challenges · Compliance & Certification: o Coordinate the manufacturer audit and certificate (e.g. ISO, CNAS, TSG, CE/FM/CSA etc.) o Manage Product certification process (e.g. CCC, CE, CPA, NEPSI etc.) o Coordinate with Notified Body, metrology bureaus and international quality departments o Ensure the implementation of the components traceability system o Implement and maintain EHS management system compliant with regulations o Guide product development follows the Siemens sustainability requirements o Coordinate the EPD (Environmental Product Declaration) o Coordinate the EcoTech analysis/report · Configuration Management: o Define the configuration management guidelines for all product development assets (e.g. source code, drawings, design documents, project documents, certificates etc.) o Conduct audit to ensure the defined configuration management guideline is properly implemented
1、可按照GSP要求建立、实施和维护企业质量管理体系，确保符合最新法规要求。 2、熟悉计算机系统验证（如温控系统、药品追溯系统等）。 3、负责供应商/客户资质审核、质量协议签订及动态管理。 4、处理药品验收、养护、退货、不合格品销毁等关键环节的质量问题。 5、主导药品不良反应报告、质量投诉、召回等突发事件的处理。 6、主导药监部门检查、飞行检查及第三方审计。 7、制定和审核质量管理文件（如操作规程SOP、质量档案、温湿度记录等）。 8、可协调业务、仓储或跨部门落实质量要求。 9、熟练使用药品经营质量管理软件（如ERP、GSP管理系统）。
1、可按照GSP要求建立、实施和维护企业质量管理体系，确保符合最新法规要求。 2、熟悉计算机系统验证（如温控系统、药品追溯系统等）。 3、负责供应商/客户资质审核、质量协议签订及动态管理。 4、处理药品验收、养护、退货、不合格品销毁等关键环节的质量问题。 5、主导药品不良反应报告、质量投诉、召回等突发事件的处理。 6、主导药监部门检查、飞行检查及第三方审计。 7、制定和审核质量管理文件（如操作规程SOP、质量档案、温湿度记录等）。 8、可协调业务、仓储或跨部门落实质量要求。 9、熟练使用药品经营质量管理软件（如ERP、GSP管理系统）。