顺丰质量经理

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。

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）。