质量工程师
常州市骏马车辆配件厂
- 公司规模：500-1000人
- 公司性质：民营公司
- 公司行业：汽车及零配件
职位信息
- 发布日期：2013-12-05
- 工作地点：常州
- 招聘人数：若干
- 职位类别：质量管理/测试工程师(QA/QC工程师)
职位描述
Title ：Quality Engineer (QMS)
Direct report to：Senior Quality Engineer
Subordinate：Micro Lab Technician
Key Responsibilities：
1. Creation and development of technical documentation as well as the management and control of a corporate Quality documentation system, including the documents, records and associated processes.
建立并发展质量体系文件及技术文档,包括各相关过程的文档和记录
2. Review and distribute the new/revised document as per document change request.
审核并分发文件变更记录所要求的新文件或修改的文件
3. Establishes and maintains a central repository, including history files, for all controlled Quality & Regulatory documents and records.
建立并维护中心文档,包括质量及法规的所有文档记录
4. Perform various duties essential to the implementation and maintenance of a regulated documentation system, including coordinating efforts for the control of new and updated Quality System procedures for ISO/QSR.
承担实施及维护法规体系文件的职责,包括根据ISO/QSR要求新建和更新程序文件
5.Ensure the consistency and quality system of Medical Device product, process, and policy documentation.
确保质量体系的产品,过程,程序文件一致性
6. Clean room monitoring monthly and data analysis.
洁净室月度监控和数据分析
7.Follow up the internal audit and external audit findings to ensure the closure timely.
跟进内审/外审的发现,确保及时关闭
8.Responsible for NEO Induction Training.
负责入职培训(质量部分)
9. In-charge of review the DHR and batch record.
负责评审DHR及批记录
10.Support QA Dept. for the daily grind, including office supply requisition and checking attendance each month by system.
支持QA部门的日常事务,包含日用品的采购,检查每月的出勤
11.Review of Sterilization report and certificate; Issue COC for outgoing goods.
审核灭菌报告,完成成品出货COC
12.Supervise and coordinate with Micro lab technician for Micro lab daily operations.
管理并协助微生物技术员负责微生物实验室的日常运行
job requirement:
1.Degree or diploma 大学或大专以上学历
2.At least 2 year experience in Micro lab as lab technician or supervisor. 至少有两年以上微生物实验技术员或主管经验。
3.Major in Pharmacy, Pharmaceutical Engineering or Microbiology 制药 / 制药工程 / 微生物学专业
Direct report to：Senior Quality Engineer
Subordinate：Micro Lab Technician
Key Responsibilities：
1. Creation and development of technical documentation as well as the management and control of a corporate Quality documentation system, including the documents, records and associated processes.
建立并发展质量体系文件及技术文档,包括各相关过程的文档和记录
2. Review and distribute the new/revised document as per document change request.
审核并分发文件变更记录所要求的新文件或修改的文件
3. Establishes and maintains a central repository, including history files, for all controlled Quality & Regulatory documents and records.
建立并维护中心文档,包括质量及法规的所有文档记录
4. Perform various duties essential to the implementation and maintenance of a regulated documentation system, including coordinating efforts for the control of new and updated Quality System procedures for ISO/QSR.
承担实施及维护法规体系文件的职责,包括根据ISO/QSR要求新建和更新程序文件
5.Ensure the consistency and quality system of Medical Device product, process, and policy documentation.
确保质量体系的产品,过程,程序文件一致性
6. Clean room monitoring monthly and data analysis.
洁净室月度监控和数据分析
7.Follow up the internal audit and external audit findings to ensure the closure timely.
跟进内审/外审的发现,确保及时关闭
8.Responsible for NEO Induction Training.
负责入职培训(质量部分)
9. In-charge of review the DHR and batch record.
负责评审DHR及批记录
10.Support QA Dept. for the daily grind, including office supply requisition and checking attendance each month by system.
支持QA部门的日常事务,包含日用品的采购,检查每月的出勤
11.Review of Sterilization report and certificate; Issue COC for outgoing goods.
审核灭菌报告,完成成品出货COC
12.Supervise and coordinate with Micro lab technician for Micro lab daily operations.
管理并协助微生物技术员负责微生物实验室的日常运行
job requirement:
1.Degree or diploma 大学或大专以上学历
2.At least 2 year experience in Micro lab as lab technician or supervisor. 至少有两年以上微生物实验技术员或主管经验。
3.Major in Pharmacy, Pharmaceutical Engineering or Microbiology 制药 / 制药工程 / 微生物学专业
公司介绍
公司成立于1998年，经过多年努力，产品国内领先