- 目錄
第1篇 生產(chǎn)質(zhì)量工程師崗位職責任職要求
生產(chǎn)質(zhì)量工程師崗位職責
崗位職責:
1、建立產(chǎn)品檢驗標準，檢驗標準培訓:
2、生產(chǎn)質(zhì)量問題處理:
3、生產(chǎn)過程質(zhì)量監(jiān)控:
4、生產(chǎn)質(zhì)量檢測設備維護:
任職資格:
1、大?；蛞陨蠈W歷，電子類理科專業(yè)優(yōu)先，2年以上工廠現(xiàn)場的質(zhì)量管理經(jīng)驗。
2、熟悉led 產(chǎn)品生產(chǎn)工藝流程、光電特性、產(chǎn)品工藝結構、產(chǎn)品質(zhì)量檢驗標準、生產(chǎn)各站質(zhì)量控制點;
3、能熟練運用各種質(zhì)量工具(qc七大手法 、5why等)分析解決客戶投訴的質(zhì)量問題、能夠熟練操作質(zhì)量檢測和分析設備、能夠組織和全面分析質(zhì)量問題;
4、較強的組織能力和溝通能力。
生產(chǎn)質(zhì)量工程師崗位
第2篇 生產(chǎn)質(zhì)量管理工程師崗位職責
職位要求:
機械設計或相關專業(yè)?？萍耙陨蠈W歷
在機加、鈑金行業(yè)擁有5年以上生產(chǎn)或質(zhì)量管理工作經(jīng)驗
精通各種機械制造工藝及工序(cnc加工/焊接/鑄造/車/銑/線切割等),能根據(jù)圖紙初步檢測零件的質(zhì)量
熟悉采購與新供應商的開發(fā)流程,熟悉深圳周邊機加、鈑金、齒輪加工、模組等非標加工的供應商,擁有此類優(yōu)質(zhì)渠道資源者優(yōu)先
熟悉電機、電機驅動及常用電氣元件采購流程
了解機械加工零件的校價、核價過程,對市場價格的變動敏感,擁有一定的商務談判、議價能力
熟悉常用辦公軟件(word, e_cel, powerpoint)的使用
有能力使用solidworks、autocad查看圖紙相關信息
有駕照者優(yōu)先
職位描述:
跟蹤產(chǎn)品制作全過程,負責產(chǎn)品工藝性驗證和質(zhì)量把控,督促生產(chǎn)進度,并及時反饋。
做好預先品管,提醒供應商生產(chǎn)過程及檢測時的品質(zhì)注意事項。
負責與供應商談判價格、品質(zhì)要求、交貨日期等,確定后下采購訂單,及時跟進進度,處理異常,確保按計劃交期交貨。
供應商資源開發(fā),定期對供應商進行審核;按供應商的加工能力、品質(zhì)質(zhì)量、交貨準時率等對其進行比對分析。
負責采購過程中的退、換貨工作,對倉庫物料的退貨等處理工作。
維護與供應商的良好合作關系,參與對供應商進行考核、評估、巡場等。
第3篇 生產(chǎn)質(zhì)量工程師崗位職責
生產(chǎn)質(zhì)量工程師 聚飛光電 深圳市聚飛光電股份有限公司,聚飛光電,聚飛 崗位職責:
1、建立產(chǎn)品檢驗標準,檢驗標準培訓:
2、生產(chǎn)質(zhì)量問題處理:
3、生產(chǎn)過程質(zhì)量監(jiān)控:
4、生產(chǎn)質(zhì)量檢測設備維護:
任職資格:
1、大?；蛞陨蠈W歷,電子類理科專業(yè)優(yōu)先,2年以上工廠現(xiàn)場的質(zhì)量管理經(jīng)驗。
2、熟悉led 產(chǎn)品生產(chǎn)工藝流程、光電特性、產(chǎn)品工藝結構、產(chǎn)品質(zhì)量檢驗標準、生產(chǎn)各站質(zhì)量控制點;
3、能熟練運用各種質(zhì)量工具(qc七大手法 、5why等)分析解決客戶投訴的質(zhì)量問題、能夠熟練操作質(zhì)量檢測和分析設備、能夠組織和全面分析質(zhì)量問題;
4、較強的組織能力和溝通能力。
第4篇 生產(chǎn)質(zhì)量管理工程師崗位職責任職要求
生產(chǎn)質(zhì)量管理工程師崗位職責
質(zhì)量工程師 項目工程師 生產(chǎn) 工程 供應商質(zhì)量管理 sqe - 無紡布 non-woven 美國醫(yī)療耗材公司因業(yè)務需求新招職位，市中心上班。
要求候選人熟悉無紡布，生產(chǎn)，質(zhì)量，工程，項目都可以?？山邮荛L三角和東南亞60%出差，。英文口語流利
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. 美國醫(yī)療耗材公司因業(yè)務需求新招職位，市中心上班。
要求候選人熟悉無紡布，生產(chǎn)，質(zhì)量，工程，項目都可以?？山邮荛L三角和東南亞60%出差，。英文口語流利
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.
生產(chǎn)質(zhì)量管理工程師崗位
