Key Job Responsibility 主要工作职责: 1.System specialist in ISO9001, ISO14001, TS16949, SA8000, C-TPAT, ISO13485...whom has rich experience on the system set up, upgrading and maintaining; 体系专家:ISO9001, ISO14001, TS16949, SA8000, C-TPAT, ISO13485…对系统的搭建、升级和维护有丰富的经验 2.Plan and implement process audit activities and the annual audit, coordinate with cross-function team on the continual improvement; 计划和实施过程审核活动和年度审核，与跨职能团队协调持续改进 3.Responsible for the preparation of the 2nd party and 3rd party system audit, and supervise the implementation of the system corrective measures, responsible for the effectiveness of corrective measures evaluation and report; 负责编制第二方和第三方体系审核，并监督体系纠正措施的实施，负责对纠正措施的有效性进行评价和报告; 4.Lead the external customer audit, 3rd party audit, Internal audit and CAP; 领导外部客户审核、第三方审核、内部审核和CAP 5.Review the standardization of company management system documents to ensure the simplification, unification, coordination and optimization of internal management standards, continuous improvement; 审核公司管理体系文件的标准化，确保内部管理标准的简化、统一、协调和优化，持续改进 6.Document review and release, Quality reporting; 文件审核和发布，质量报告 7.Initiation, implementation and control of factory manufacture process corrective action and proventive actions. 发起，实施和控制工厂生产过程的纠正措施和预防措施 8.Implementation and continuous improvement of all Sigma factories related incident management (CAP). 实施并持续改进所有Sigma工厂相关事件管理(CAP) 9.Establishment, operation and maintenance of hazardous substances management system (collect relevant regulations and customer standards, and provide relevant environmental protection information to customers) 有害物质管理体系的建立、运行和维护(收集相关法规和客户标准，并向客户提供相关环保信息) Qualification Requirements资质要求: 1.Very good commands of English (Both orally & written); 良好的英语听说读写能力 2.Good computer skills on Microsoft office series; 熟练使用微软办公软件 3.Very familiar with ISO9001, ISO9001, ISO14001,SA8000, C-TPAT, TS16949, ISO13485...; 熟悉ISO9001、ISO9001、ISO14001、SA8000、C-TPAT、TS16949等 4.Very good systematic and Closed Loop thinking; 非常好的系统和闭环思维 5.DCC experience; DCC经验 6.Can communicate with peoples and the skills are good. 能与人沟通，技能较好 7.Experience in electronics industry is required 需要有电子行业的从业经验

Key Job Responsibility 主要工作职责: 1.System specialist in ISO9001, ISO14001, TS16949, SA8000, C-TPAT, ISO13485...whom has rich experience on the system set up, upgrading and maintaining; 体系专家:ISO9001, ISO14001, TS16949, SA8000, C-TPAT, ISO13485…对系统的搭建、升级和维护有丰富的经验 2.Plan and implement process audit activities and the annual audit, coordinate with cross-function team on the continual improvement; 计划和实施过程审核活动和年度审核，与跨职能团队协调持续改进 3.Responsible for the preparation of the 2nd party and 3rd party system audit, and supervise the implementation of the system corrective measures, responsible for the effectiveness of corrective measures evaluation and report; 负责编制第二方和第三方体系审核，并监督体系纠正措施的实施，负责对纠正措施的有效性进行评价和报告; 4.Lead the external customer audit, 3rd party audit, Internal audit and CAP; 领导外部客户审核、第三方审核、内部审核和CAP 5.Review the standardization of company management system documents to ensure the simplification, unification, coordination and optimization of internal management standards, continuous improvement; 审核公司管理体系文件的标准化，确保内部管理标准的简化、统一、协调和优化，持续改进 6.Document review and release, Quality reporting; 文件审核和发布，质量报告 7.Initiation, implementation and control of factory manufacture process corrective action and proventive actions. 发起，实施和控制工厂生产过程的纠正措施和预防措施 8.Implementation and continuous improvement of all Sigma factories related incident management (CAP). 实施并持续改进所有Sigma工厂相关事件管理(CAP) 9.Establishment, operation and maintenance of hazardous substances management system (collect relevant regulations and customer standards, and provide relevant environmental protection information to customers) 有害物质管理体系的建立、运行和维护(收集相关法规和客户标准，并向客户提供相关环保信息) Qualification Requirements资质要求: 1.Very good commands of English (Both orally & written); 良好的英语听说读写能力 2.Good computer skills on Microsoft office series; 熟练使用微软办公软件 3.Very familiar with ISO9001, ISO9001, ISO14001,SA8000, C-TPAT, TS16949, ISO13485...; 熟悉ISO9001、ISO9001、ISO14001、SA8000、C-TPAT、TS16949等 4.Very good systematic and Closed Loop thinking; 非常好的系统和闭环思维 5.DCC experience; DCC经验 6.Can communicate with peoples and the skills are good. 能与人沟通，技能较好 7.Experience in electronics industry is required 需要有电子行业的从业经验

岗位职责： 1、负责维护公司质量管理体系的程序指引文件符合性和有效性； 2、与相关方定时沟通确保取得新标准及要求； 3、评审外来文件的适用性； 4、 以系统的思维协助及指导内部相关部门完成纠正措施方案； 5、监视客户反馈信息以至传达到内部相关单位； 6、持续改进及优化质量系统； 7、工作地点可接受江门台山市。 岗位要求： 1、大专或以上学历，专业不限，具备3年以上汽车制造行业经验，及1年质量相关工作经验； 2、办公软件操作熟练，英语能力熟练优先考虑； 3、熟悉ISO, IATF16949,专业知识，对体系与审核工具有一定的观念以及技巧； 4、具备一定的数据分析及基本质量工具使用能力； 5、思维敏捷，反应迅速、逻辑思维能力强； 6、良好的沟通、协调能力，语言表达能力强； 7、个性活泼开朗，能够承受工作压力，能独立完成工作。

职位概要(Job summary): Quasar’s Program Management Team comprising of Program managers and Program Specialists, manage and are responsible for P&L for designated Programs as well for ensuring Excellent Customer Experience. As a Program Specialist, you will work together with Program Manager to ensure a program meet Customer expectations – defined by On Time Delivery, Quality of products delivered and providing Excellent Customer Support. Program Specialists work with KAM, Quality, Manufacturing, Finance, and other functions across Quasar as well as Customer. 工作职责(Responsibilities): 1. Support Program Manager for reach P&L Targets for assigned program. 2. Maintain excellent relationship with customers by coordinating internal activities and providing timely updates. 3. Suggest and / or manage implementation of cost reduction initiatives. 4. Receive and Manage Customer POs from receiving till fulfilment. 5. Maintain accurate costing files for each program. 6. Manage changes in scope of program that will affect cost and scheduling of orders. 7. Coordinate with Finance Department on Payment issues. 8. Other tasks assigned by superior. 任职资格(Qualification) : Educational Background and Experience 1. Bachelor and above. 2. 5 more years of experience as Program Specialist / Customer Service Specialist in Medical Device / Electronic Industry. Skills and Competencies 1. Good Communication Skills to manage internal and external communications. 2. Knowledge of FDA regulations preferred 3. Must be results-oriented 4. Demonstrated ability to successfully support multiple programs and meet targets for P&L and Customer Satisfaction. 5. Demonstrated proficiency in Microsoft Office Tools is required.

职位概要(Job summary): The Regulatory Compliance Sr. Engineer is to monitor and ensure the compliance to external standards/requirements and Quasar Quality System Requirements in Quasar manufacturing site. 工作职责(Responsibilities): 1. Conduct routine monitoring, checking program to identify site compliance gaps and follow up gap remediation. 2. Participate in Corporate Procedure Development & Maintenance. Join Corporate audit on other sites when required. 3. Provide Regulation Compliance supporting on critical business projects, when necessary, e.g., MAH 4. Facilitate critical external audits/inspection at site. e.g., FDA inspection, NMPA audits. 5. Join cross sites QMS IT system coordination and maintenance. 6. Responsible for liaising with the company’s internal/external stakeholders to identify/understand the required Regulatory Compliance knowledge needed to provide the required expertise and advice. 7. Other tasks assigned by leader. 任职资格(Qualification) : 1. Bachelor or Master’s degree in science related field. 2. Minimum of 5 years’ experiences on Medical Device or Pharmaceutical Industry Quality Regulatory Compliance related work. Knowledgeable on international standards or Health Authorities regulations requirement. 3. Good oral and written communication skills both in English and Chinese. 4. Good interpersonal and influential skills. 5. Ability to work under pressure in a dynamic environment.

工作内容： 1、维护公司体系正常运转，并对其进行持续优化；主导每年内审、管理评审的策划及跟踪改善； 2、主导新老客户/第三方审核员对公司进行的质量、环保、双碳、QSA/QPA/年度等体系的审核，以及跟踪回复； 3、监管品质部门的文控、SQE、IQC相关人员的日常工作； 4、主导负责推行公司5S改善，组织策划管理活动，及评估现场检查及和改善跟踪现场问题； 岗位要求： 1、本科以上学历，男女不限、身体健康、年龄在30-50岁之间； 2、有TS/ISO内审三证资格证（有外审资格证优先）； 3、从事体系专员/主任岗位5年以上工作经验； 4、有良好的沟通能力，有责任担当，改善推动力强； 5、有英语基础，具备基本的读&写能力；