- 目录
第1篇 质量体系专员职位描述与岗位职责任职要求
职位描述：
1.本科学历：药学、生物技术或生物工程等相关专业；
2.两年以上医药/医药包装/医疗器械行业质量体系管理经验，参加过内审和外部审核；
3.熟悉iso 9001、iso 13485、cfda、 gmp质量管理体系，接受过iso13485 或iso19001的培训，具有内审员资格；
4.熟练使用各种办公软件，如：sap， word， e_cel， outlook;
5.能流利的阅读和书写英语；
6.文字表达能力强，能独立建设、编写、汇档体系文件；
7.认真细致，良好的沟通能力和亲和力，责任心强，有团队协作精神，良好的职业操守和敬业精神。
第2篇 质量体系建设专员岗位职责
质量体系建设高级专员 吉利汽车 浙江吉利控股集团有限公司,吉利控股集团,吉利控股集团有限公司,吉利新能源,吉利汽车,吉利集团 工作职责:
建立和维护质量管理体系
任职要求:
1)大学本科毕业,工科背景;
2)4年以上汽车或知名零部件企业质量经历;
3)熟悉iatf16949体系建立及运行;
4)有与欧美或日系主机厂配套供货经验。
第3篇 质量体系管理专员岗位职责任职要求
质量体系管理专员岗位职责
质量体系高级专员-供应商管理qs sr. specialist 诺化仕(无锡)制药有限公司 诺化仕(无锡)制药有限公司，诺化仕 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.
质量体系管理专员岗位
第4篇 qmo specialist质量体系专员岗位职责描述岗位要求
职位描述：
职责描述：
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
职位要求：
第5篇 质量体系管理专员岗位职责
质量体系管理专员 景兴健护 广东景兴健康护理实业股份有限公司,abc,广东景兴,景兴健护,景兴 主要职责:
1、负责公司所有质量管理体系文件及表单的归口管理及定期评审。
2、负责体系文件培训宣贯,促进各部门及时学习质量体系文件和相关标准法规。
3、协助质量体系年度审核工作安排,协助开展滚动式质量体系有效性检查。
4、负责对工作相关的重要文件资料作及时完善、整理、归档。
5、负责研发中心相关制度流程的修改跟进。
6、负责原材料样板、供应商资料(如msds、coa等)的接收、归档、整理工作。
7、协助供应商现场审核的工作,跟踪验证供应商的整改情况。
8、协助工作:部门日常团建活动、协助各组及上司完成部门行政工作。
任职要求:
1、大专及以上学历,1年以上卫生用品、医药、食品、化妆品等相关行业质量体系管理的工作经验。
2、熟悉iso或者gmp等知识,了解相关行业生产、质量流程。
