生产质量工程师岗位职责4篇

第1篇 生产质量工程师岗位职责任职要求

生产质量工程师岗位职责

岗位职责:

1、建立产品检验标准，检验标准培训:

2、生产质量问题处理:

3、生产过程质量监控:

4、生产质量检测设备维护:

任职资格:

1、大专或以上学历，电子类理科专业优先，2年以上工厂现场的质量管理经验。

2、熟悉led 产品生产工艺流程、光电特性、产品工艺结构、产品质量检验标准、生产各站质量控制点;

3、能熟练运用各种质量工具(qc七大手法 、5why等)分析解决客户投诉的质量问题、能够熟练操作质量检测和分析设备、能够组织和全面分析质量问题;

4、较强的组织能力和沟通能力。

生产质量工程师岗位

第2篇 生产质量管理工程师岗位职责

职位要求:

机械设计或相关专业专科及以上学历

在机加、钣金行业拥有5年以上生产或质量管理工作经验

精通各种机械制造工艺及工序(cnc加工/焊接/铸造/车/铣/线切割等),能根据图纸初步检测零件的质量

熟悉采购与新供应商的开发流程,熟悉深圳周边机加、钣金、齿轮加工、模组等非标加工的供应商,拥有此类优质渠道资源者优先

熟悉电机、电机驱动及常用电气元件采购流程

了解机械加工零件的校价、核价过程,对市场价格的变动敏感,拥有一定的商务谈判、议价能力

熟悉常用办公软件(word, e_cel, powerpoint)的使用

有能力使用solidworks、autocad查看图纸相关信息

有驾照者优先

职位描述:

跟踪产品制作全过程,负责产品工艺性验证和质量把控,督促生产进度,并及时反馈。

做好预先品管,提醒供应商生产过程及检测时的品质注意事项。

负责与供应商谈判价格、品质要求、交货日期等,确定后下采购订单,及时跟进进度,处理异常,确保按计划交期交货。

供应商资源开发,定期对供应商进行审核;按供应商的加工能力、品质质量、交货准时率等对其进行比对分析。

负责采购过程中的退、换货工作,对仓库物料的退货等处理工作。

维护与供应商的良好合作关系,参与对供应商进行考核、评估、巡场等。

第3篇 生产质量工程师岗位职责

生产质量工程师 聚飞光电 深圳市聚飞光电股份有限公司,聚飞光电,聚飞 岗位职责:

1、建立产品检验标准,检验标准培训:

2、生产质量问题处理:

3、生产过程质量监控:

4、生产质量检测设备维护:

任职资格:

1、大专或以上学历,电子类理科专业优先,2年以上工厂现场的质量管理经验。

2、熟悉led 产品生产工艺流程、光电特性、产品工艺结构、产品质量检验标准、生产各站质量控制点;

3、能熟练运用各种质量工具(qc七大手法 、5why等)分析解决客户投诉的质量问题、能够熟练操作质量检测和分析设备、能够组织和全面分析质量问题;

4、较强的组织能力和沟通能力。

第4篇 生产质量管理工程师岗位职责任职要求

生产质量管理工程师岗位职责

质量工程师 项目工程师 生产 工程 供应商质量管理 sqe - 无纺布 non-woven 美国医疗耗材公司因业务需求新招职位，市中心上班。

要求候选人熟悉无纺布，生产，质量，工程，项目都可以。可接受长三角和东南亚60%出差，。英文口语流利

job description

1. establish detailed product， material， manufacturing and inspection specifications for drapes and gowns (non-woven). prepare the detailed specifications for new supplier/new product development.

2. establish and meet new development project schedules， work close with supplier development teams and manage the projects to achieve target date and objectives.

3. review manufacturing process and translate to workable procedures， responsibilities include but not limited to the setup ofproduct specifications， setup of process control， setup of inspection criteria， supplier trainings， process validations， etc.

4. work closely with suppliers， the shanghai office and the corporate office in the usa to lead product changes and improvements.

5. be responsible for quality control of the products manufactured by supplier factories， responsibilities include but are not limited to process audits， capas， deviations， calibrations， inspections， trainings， maintenance， environmental control， data collection and analysis， development of quality related methodology， etc.

6. lead the root cause investigations and analysis for quality issues such as customer complaints and inspection rejections. implement solutions to reduce complaint numbers. ensure that solutions to quality issues are properly implemented and upheld.

7. identify opportunities and implement activities for continuous improvement. for e_ample， upon initial setup， assist in resolving issues and helping inefficiencies

qualifications:

1. b.s. degree in engineering， background in non-woven manufacturing is preferred.

2. fluent in english is a must.

3. 2+ years of e_perience in process control and quality control is required， preferably with relevant e_perience in medical device industries.

4. detail oriented with strong communication， problem solving， and organizational skills.

5. professional attitude with a heightened sense of urgency to complete tasks accurately and efficiently.

6. proficiency of pc skills: ms word， ms e_cel， adobe and e-mail， autocad or solidworks is a plus. 美国医疗耗材公司因业务需求新招职位，市中心上班。

要求候选人熟悉无纺布，生产，质量，工程，项目都可以。可接受长三角和东南亚60%出差，。英文口语流利

job description

1. establish detailed product， material， manufacturing and inspection specifications for drapes and gowns (non-woven). prepare the detailed specifications for new supplier/new product development.

2. establish and meet new development project schedules， work close with supplier development teams and manage the projects to achieve target date and objectives.

3. review manufacturing process and translate to workable procedures， responsibilities include but not limited to the setup ofproduct specifications， setup of process control， setup of inspection criteria， supplier trainings， process validations， etc.

4. work closely with suppliers， the shanghai office and the corporate office in the usa to lead product changes and improvements.

5. be responsible for quality control of the products manufactured by supplier factories， responsibilities include but are not limited to process audits， capas， deviations， calibrations， inspections， trainings， maintenance， environmental control， data collection and analysis， development of quality related methodology， etc.

6. lead the root cause investigations and analysis for quality issues such as customer complaints and inspection rejections. implement solutions to reduce complaint numbers. ensure that solutions to quality issues are properly implemented and upheld.

7. identify opportunities and implement activities for continuous improvement. for e_ample， upon initial setup， assist in resolving issues and helping inefficiencies

qualifications:

1. b.s. degree in engineering， background in non-woven manufacturing is preferred.

2. fluent in english is a must.

3. 2+ years of e_perience in process control and quality control is required， preferably with relevant e_perience in medical device industries.

4. detail oriented with strong communication， problem solving， and organizational skills.

5. professional attitude with a heightened sense of urgency to complete tasks accurately and efficiently.

6. proficiency of pc skills: ms word， ms e_cel， adobe and e-mail， autocad or solidworks is a plus.

生产质量管理工程师岗位