Job Descriptions :
I. Management System Operation
一.管理体系运行
1.Overall responsibility for the quality management of the department; participate in or independently conduct the formulation, revision, and promotion of quality manuals, procedures, quality-related work instructions, and record forms.
总体负责所在部门的质量管理工作，参与或独立进行质量手册、程序文件、质量相关工作指引、记录表单的编制、修订及宣贯工作
2.Responsible for the operation and implementation of the management system in the department; ensure all quality activities of the business comply with accreditation standards such as ISO/IEC 17025, ISO/IEC 17065, ISO/IEC 17029, ISO 9001, and relevant accreditation and evaluation recognition criteria.
负责所在部门的管理体系运行及实施，推动业务部门的各项质量活动满足认可质量标准，如ISO/IEC 17025, ISO/IEC 17065，ISO/IEC 17029, ISO 9001等标准，以及相关认可机构的认可准则/评审准则等的要求
3.Cooperate with the corporate quality management department to complete conduct internal audits; independently perform assigned internal audit tasks including organizing internal audits, developing audit plans, conducting audits, and issuing audit reports; independently carry out department-level special specified internal audits when necessary.
配合总公司质量管理部门完成内审工作，独立完成指定范围内的内审任务，包括但不限于；组织内部审核工作，编写内部审核计划、实施内审及形成报告；必要时，独立开展部门级专项内部审核
4.Support the corporate quality department in management review; assist in organizing management reviews, preparing review plans and reports, and implementing improvement and follow-up actions.
配合总公司质量管理部门完成管理评审工作，协助组织实施管理评审，编写管理评审计划和评审报告，以及所制定的改进/跟进措施的实施；
5.Responsible for the investigation, handling, and verification of corrective actions for customer complaints and quality incidents.
负责客户投诉、质量事故的调查、处理及整改结果的验证
6.Manage non-conformities and track the implementation and effectiveness of corrective actions; identify risks and opportunities in laboratory activities, develop response corresponding measures, and supervise monitoring implementation and verify effectiveness check.
负责组织对不符合项的控制，并对纠正措施的执行情况进行跟踪验证；识别实验室活动中的风险与机遇，制定应对措施，并监督执行和验证措施的有效性
7.Develop, implement, and monitor the effectiveness of quality improvement measures.
质量改进措施的制定，实施和效果监控
II. Qualification Acquisition
二.资质获取
1.Track and study accreditation requirements from relevant bodies authorities; collect and update external regulations, laws, and testing standards; organize internal training and promotion as needed.
组织和学习本部门涉及的认可机构的相关认可要求，包括：跟踪外部监管及认可机构文件、法律法规收集、跟踪检测标准的查新工作等，并按需组织部门内部培训和宣贯
2.Coordinate company-level qualification accreditation applications and expansions for the department, including CNAS, CMA, CBTL, A2LA, DAkkS, and other domestic and international authorities bodies (NB, CB, testing, inspection bodies, etc.); communicate with external accreditation bodies and coordinate with audit teams during on-site assessments.
总体协调本部门相关各项公司级（当地公司及国内外NB，CB，检测机构，检验机构等）资质申请和资质扩充，包括CNAS/CMA/CBTL/A2LA/DAkkS等，包括：与相关各类外部认可机构的沟通工作以及在具体的外部审核及检查中，负责与评审组的沟通协调工作；协调本部门资源配合评审组工作，包括：申请前准备，审核应对，审核后整改及追踪
3.Coordinate department resources for audit preparation, response on-site audit, post-audit implements corrective actions, and follow-up
主导并协助本部门获取专项的外部认可资质，支持本部门产品/服务满足相关国际市场准入要求
Ⅲ. Cross-department Support & Others
三.跨地区/部门支持及其它
1.Provide cross-department and cross-location support for management system operation and qualification acquisition as assigned by leadership.
根据领导安排及部门需要，跨部门和地址支持管理体系运行及资质获取工作
2.Support departmental HSE-related work as required.
根据领导安排及部门需要，支持部门HSE相关工作
3.Complete other tasks assigned by the supervisor.
完成领导交办的其他工作
Job Requirements：
1.Bachelor degree or above, major in Engineering related or Quality Management.
本科及以上学历，工程类或质量管理相关专业
2.Familiar with ISO/IEC 17025 and 17065, have basic knowledge of ISO/IEC 17020, 17029, 17021 and relevant support standards including ISO/IEC 17000, 17067, etc.
熟悉 ISO/IEC 17025、17065，掌握 ISO/IEC 17020、17029、17021 及 ISO/IEC 17000、17067 等相关支持标准的基础知识
3.Familiar with qualify management.
熟悉质量管理体系
4.Good communication/coordination skill which could support handling complex projects and cross department cooperation.
具备良好的沟通协调能力，能够支撑复杂项目推进及跨部门协作
5.With 5 years working experience in TIC industry qualify management.
拥有 5 年 TIC 行业（检测、检验、认证）质量管理相关工作经验
6.Good at Speaking and writing in English.
英语听说读写流利
In the Products division at TÜV Rheinland, we are looking for talented individuals who want to join us at the forefront of safety, quality, and innovation. Our goal is to ensure that products on international markets are safe and compliant with standards—from consumer goods to highly complex medical devices. In doing so, we help companies meet national and international standards.
Equal opportunities are particularly important to us at TÜV Rheinland. We are committed to breaking down barriers and creating an inclusive working environment characterised by respect, diversity and genuine participation. We therefore particularly welcome applications from people with severe disabilities.
Join a strong team! At TÜV Rheinland, you can apply and expand your expertise in an international setting. We offer a dynamic work environment that fosters innovation and is committed to diversity and continuous learning. Together, we are shaping a future where safety and quality go hand in hand.
