- 目錄
第1篇 質(zhì)量體系專(zhuān)員職位描述與崗位職責(zé)任職要求
職位描述：
1.本科學(xué)歷：藥學(xué)、生物技術(shù)或生物工程等相關(guān)專(zhuān)業(yè)；
2.兩年以上醫(yī)藥/醫(yī)藥包裝/醫(yī)療器械行業(yè)質(zhì)量體系管理經(jīng)驗(yàn)，參加過(guò)內(nèi)審和外部審核；
3.熟悉iso 9001、iso 13485、cfda、 gmp質(zhì)量管理體系，接受過(guò)iso13485 或iso19001的培訓(xùn)，具有內(nèi)審員資格；
4.熟練使用各種辦公軟件，如：sap， word， e_cel， outlook;
5.能流利的閱讀和書(shū)寫(xiě)英語(yǔ)；
6.文字表達(dá)能力強(qiáng)，能獨(dú)立建設(shè)、編寫(xiě)、匯檔體系文件；
7.認(rèn)真細(xì)致，良好的溝通能力和親和力，責(zé)任心強(qiáng)，有團(tuán)隊(duì)協(xié)作精神，良好的職業(yè)操守和敬業(yè)精神。
第2篇 質(zhì)量體系建設(shè)專(zhuān)員崗位職責(zé)
質(zhì)量體系建設(shè)高級(jí)專(zhuān)員 吉利汽車(chē) 浙江吉利控股集團(tuán)有限公司,吉利控股集團(tuán),吉利控股集團(tuán)有限公司,吉利新能源,吉利汽車(chē),吉利集團(tuán) 工作職責(zé):
建立和維護(hù)質(zhì)量管理體系
任職要求:
1)大學(xué)本科畢業(yè),工科背景;
2)4年以上汽車(chē)或知名零部件企業(yè)質(zhì)量經(jīng)歷;
3)熟悉iatf16949體系建立及運(yùn)行;
4)有與歐美或日系主機(jī)廠配套供貨經(jīng)驗(yàn)。
第3篇 質(zhì)量體系管理專(zhuān)員崗位職責(zé)任職要求
質(zhì)量體系管理專(zhuān)員崗位職責(zé)
質(zhì)量體系高級(jí)專(zhuān)員-供應(yīng)商管理qs sr. specialist 諾化仕(無(wú)錫)制藥有限公司 諾化仕(無(wú)錫)制藥有限公司，諾化仕 job responsibilities:
1. supplier management: management of supplier related sop and wi; guide for the supplier qualification process; generate annual supplier audit plan and report; e_ecute and organize supplier audits; generate supplier audit reports; follow-up the capa actions with supplier; follow-up the stauts of supplier; annual evaluation of suppliers; keep and maintence the supplier list;
2. qs management: update qs of gmp related materials and products;
3. support and participate the self-inspection of site;
4. follow-up the inter audit (corporate) actions and report;
5. supplier dossier management;
6. other supplier management related works from corporate;
7. other assigned works.
job requirements:
1. e_perienced with supplier management in a gmp condition; familiar with gmp and iso9001， and related standards;
2. have the e_perience of gmp self-inspection;
3. good communication and coordination ability;
4. good learning capacity， can learn novacyl procedure smoothly;
5. good with team work， e_ecutive force;
6. can handle pressure from workload;
7. english writing and read ;
8. skillful using microsoft word， e_cel， ppt， windows， etc;
9. basic knowledge about gmp， safty and chemical.
質(zhì)量體系管理專(zhuān)員崗位
第4篇 qmo specialist質(zhì)量體系專(zhuān)員崗位職責(zé)描述崗位要求
職位描述：
職責(zé)描述：
summary
?develop and continual improvement of the quality management system and support the governance of business process.
?ensure e_ecution of proper internal audits to all corporate functions for measuring company’s compliance to the quality system as required by the relevant iso/vda standards.
?support both company and project requirements in driving quality assurance into processes， procedures and departmental activities.
duties and responsibilities
(these are the positions essential duties and is not an all-inclusive list)
main areas of responsibilities are:
?ensure a proper quality management system based on the global one is in place and controlled in compliance with iso/vda relevant standards.
?participate in the development of the quality management system based on business processes and their continuous improvement.
?coordinate local certifications with certification bodies and manage e_ternal audits.
?ensure compliance to quality management system and related iso/vda standards by establishing and performing internal audits that measure the effectiveness of the systems; including management of local and cross-country audit plans.
?ensure that quality management system documentation is updated according to guidelines.
?ensure effective e_ecution of the processes milestones (qamm) throughout the project from kick-off to close-out.
?support qmo manager in the implementation of common quality methodologies， tools and information systems， their continuous improvement and alignment on best practices.
?support qmo manager in the monitoring of quality kpis， the analysis of results and the development and monitoring of improvement plans.
?assure lessons learned and nonconformity process are facilitated and driven back into the business processes for continuous improvement.
?responsible to identify and communicate quality general concerns and or issues to appropriate department.
?support continuous improvement activities e.g.， kaizen， 5s， si_ sigma projects， value engineering， lean manufacturing， etc.
knowledge & skills
?knowledge of quality management system， methodologies， tools， best practices， etc.
?knowledge of iso/vda standards principles within the scope of application.
?comau quality management system and business processes， procedures and instructions.
?iso 9001/vda 6.4 internal auditor certification.
?understanding of general corporate operations and business (multiple bu e_perience is a plus).
?quality philosophies – basic principles and practices
?management systems standards
?comau quality foundations
?quality kpi (key performance indicators)
?quality-specific it tools
?management system auditing skills
?supplier auditing skills
?general knowledge of wcm qc-pillar
?problem solving: defect analysis and prevention，
?reliability and risk management
?customer specifications (technical and regulatory)
?outline of product development process / milestones and quality gates management
?chargeback
behavioral competencies
?teamwork with cross functional teams
?communication skills， verbal， written and follow-up
?ability to interface in a multicultural environment.
?business awareness
?managing relationships
?communication
?personal organization
?change minded & driven
qualifications
?education :
obachelor degree in engineering required and organization and industry e_perience.
?previous e_periences
oa minimum of 3 years in quality assurance or process quality management e_perience in the automotive or allied industry.
oe_periences in engineering/manufacturing environment preferred.
?languages
oenglish: fluent
職位要求：
第5篇 質(zhì)量體系管理專(zhuān)員崗位職責(zé)
質(zhì)量體系管理專(zhuān)員 景興健護(hù) 廣東景興健康護(hù)理實(shí)業(yè)股份有限公司,abc,廣東景興,景興健護(hù),景興 主要職責(zé):
1、負(fù)責(zé)公司所有質(zhì)量管理體系文件及表單的歸口管理及定期評(píng)審。
2、負(fù)責(zé)體系文件培訓(xùn)宣貫,促進(jìn)各部門(mén)及時(shí)學(xué)習(xí)質(zhì)量體系文件和相關(guān)標(biāo)準(zhǔn)法規(guī)。
3、協(xié)助質(zhì)量體系年度審核工作安排,協(xié)助開(kāi)展?jié)L動(dòng)式質(zhì)量體系有效性檢查。
4、負(fù)責(zé)對(duì)工作相關(guān)的重要文件資料作及時(shí)完善、整理、歸檔。
5、負(fù)責(zé)研發(fā)中心相關(guān)制度流程的修改跟進(jìn)。
6、負(fù)責(zé)原材料樣板、供應(yīng)商資料(如msds、coa等)的接收、歸檔、整理工作。
7、協(xié)助供應(yīng)商現(xiàn)場(chǎng)審核的工作,跟蹤驗(yàn)證供應(yīng)商的整改情況。
8、協(xié)助工作:部門(mén)日常團(tuán)建活動(dòng)、協(xié)助各組及上司完成部門(mén)行政工作。
任職要求:
1、大專(zhuān)及以上學(xué)歷,1年以上衛(wèi)生用品、醫(yī)藥、食品、化妝品等相關(guān)行業(yè)質(zhì)量體系管理的工作經(jīng)驗(yàn)。
2、熟悉iso或者gmp等知識(shí),了解相關(guān)行業(yè)生產(chǎn)、質(zhì)量流程。
