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Key Job Responsibility 主要工作職責(zé): 1.System specialist in ISO9001, ISO14001, TS16949, SA8000, C-TPAT, ISO13485...whom has rich experience on the system set up, upgrading and maintaining; 體系專(zhuān)家:ISO9001, ISO14001, TS16949, SA8000, C-TPAT, ISO13485…對(duì)系統(tǒng)的搭建、升級(jí)和維護(hù)有豐富的經(jīng)驗(yàn) 2.Plan and implement process audit activities and the annual audit, coordinate with cross-function team on the continual improvement; 計(jì)劃和實(shí)施過(guò)程審核活動(dòng)和年度審核，與跨職能團(tuán)隊(duì)協(xié)調(diào)持續(xù)改進(jìn) 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; 負(fù)責(zé)編制第二方和第三方體系審核，并監(jiān)督體系糾正措施的實(shí)施，負(fù)責(zé)對(duì)糾正措施的有效性進(jìn)行評(píng)價(jià)和報(bào)告; 4.Lead the external customer audit, 3rd party audit, Internal audit and CAP; 領(lǐng)導(dǎo)外部客戶(hù)審核、第三方審核、內(nèi)部審核和CAP 5.Review the standardization of company management system documents to ensure the simplification, unification, coordination and optimization of internal management standards, continuous improvement; 審核公司管理體系文件的標(biāo)準(zhǔn)化，確保內(nèi)部管理標(biāo)準(zhǔn)的簡(jiǎn)化、統(tǒng)一、協(xié)調(diào)和優(yōu)化，持續(xù)改進(jìn) 6.Document review and release, Quality reporting; 文件審核和發(fā)布，質(zhì)量報(bào)告 7.Initiation, implementation and control of factory manufacture process corrective action and proventive actions. 發(fā)起，實(shí)施和控制工廠(chǎng)生產(chǎn)過(guò)程的糾正措施和預(yù)防措施 8.Implementation and continuous improvement of all Sigma factories related incident management (CAP). 實(shí)施并持續(xù)改進(jìn)所有Sigma工廠(chǎng)相關(guān)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) 有害物質(zhì)管理體系的建立、運(yùn)行和維護(hù)(收集相關(guān)法規(guī)和客戶(hù)標(biāo)準(zhǔn)，并向客戶(hù)提供相關(guān)環(huán)保信息) Qualification Requirements資質(zhì)要求: 1.Very good commands of English (Both orally & written); 良好的英語(yǔ)聽(tīng)說(shuō)讀寫(xiě)能力 2.Good computer skills on Microsoft office series; 熟練使用微軟辦公軟件 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; 非常好的系統(tǒng)和閉環(huán)思維 5.DCC experience; DCC經(jīng)驗(yàn) 6.Can communicate with peoples and the skills are good. 能與人溝通，技能較好 7.Experience in electronics industry is required 需要有電子行業(yè)的從業(yè)經(jīng)驗(yàn)

Key Job Responsibility 主要工作職責(zé): 1.System specialist in ISO9001, ISO14001, TS16949, SA8000, C-TPAT, ISO13485...whom has rich experience on the system set up, upgrading and maintaining; 體系專(zhuān)家:ISO9001, ISO14001, TS16949, SA8000, C-TPAT, ISO13485…對(duì)系統(tǒng)的搭建、升級(jí)和維護(hù)有豐富的經(jīng)驗(yàn) 2.Plan and implement process audit activities and the annual audit, coordinate with cross-function team on the continual improvement; 計(jì)劃和實(shí)施過(guò)程審核活動(dòng)和年度審核，與跨職能團(tuán)隊(duì)協(xié)調(diào)持續(xù)改進(jìn) 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; 負(fù)責(zé)編制第二方和第三方體系審核，并監(jiān)督體系糾正措施的實(shí)施，負(fù)責(zé)對(duì)糾正措施的有效性進(jìn)行評(píng)價(jià)和報(bào)告; 4.Lead the external customer audit, 3rd party audit, Internal audit and CAP; 領(lǐng)導(dǎo)外部客戶(hù)審核、第三方審核、內(nèi)部審核和CAP 5.Review the standardization of company management system documents to ensure the simplification, unification, coordination and optimization of internal management standards, continuous improvement; 審核公司管理體系文件的標(biāo)準(zhǔn)化，確保內(nèi)部管理標(biāo)準(zhǔn)的簡(jiǎn)化、統(tǒng)一、協(xié)調(diào)和優(yōu)化，持續(xù)改進(jìn) 6.Document review and release, Quality reporting; 文件審核和發(fā)布，質(zhì)量報(bào)告 7.Initiation, implementation and control of factory manufacture process corrective action and proventive actions. 發(fā)起，實(shí)施和控制工廠(chǎng)生產(chǎn)過(guò)程的糾正措施和預(yù)防措施 8.Implementation and continuous improvement of all Sigma factories related incident management (CAP). 實(shí)施并持續(xù)改進(jìn)所有Sigma工廠(chǎng)相關(guān)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) 有害物質(zhì)管理體系的建立、運(yùn)行和維護(hù)(收集相關(guān)法規(guī)和客戶(hù)標(biāo)準(zhǔn)，并向客戶(hù)提供相關(guān)環(huán)保信息) Qualification Requirements資質(zhì)要求: 1.Very good commands of English (Both orally & written); 良好的英語(yǔ)聽(tīng)說(shuō)讀寫(xiě)能力 2.Good computer skills on Microsoft office series; 熟練使用微軟辦公軟件 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; 非常好的系統(tǒng)和閉環(huán)思維 5.DCC experience; DCC經(jīng)驗(yàn) 6.Can communicate with peoples and the skills are good. 能與人溝通，技能較好 7.Experience in electronics industry is required 需要有電子行業(yè)的從業(yè)經(jīng)驗(yàn)

職位概要(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. 工作職責(zé)(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. 任職資格(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.

職位概要(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. 工作職責(zé)(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. 任職資格(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.

崗位職責(zé)： 1、負(fù)責(zé)維護(hù)公司質(zhì)量管理體系的程序指引文件符合性和有效性； 2、與相關(guān)方定時(shí)溝通確保取得新標(biāo)準(zhǔn)及要求； 3、評(píng)審?fù)鈦?lái)文件的適用性； 4、?以系統(tǒng)的思維協(xié)助及指導(dǎo)內(nèi)部相關(guān)部門(mén)完成糾正措施方案； 5、監(jiān)視客戶(hù)反饋信息以至傳達(dá)到內(nèi)部相關(guān)單位； 6、持續(xù)改進(jìn)及優(yōu)化質(zhì)量系統(tǒng)； 7、工作地點(diǎn)可接受江門(mén)臺(tái)山市。 崗位要求： 1、大專(zhuān)或以上學(xué)歷，專(zhuān)業(yè)不限，具備3年以上汽車(chē)制造行業(yè)經(jīng)驗(yàn)，及1年質(zhì)量相關(guān)工作經(jīng)驗(yàn)； 2、辦公軟件操作熟練，英語(yǔ)能力熟練優(yōu)先考慮； 3、熟悉ISO,?IATF16949,專(zhuān)業(yè)知識(shí)，對(duì)體系與審核工具有一定的觀(guān)念以及技巧； 4、具備一定的數(shù)據(jù)分析及基本質(zhì)量工具使用能力； 5、思維敏捷，反應(yīng)迅速、邏輯思維能力強(qiáng)； 6、良好的溝通、協(xié)調(diào)能力，語(yǔ)言表達(dá)能力強(qiáng)； 7、個(gè)性活潑開(kāi)朗，能夠承受工作壓力，能獨(dú)立完成工作。