日日噜夜夜草|一级黄色录像高清版|调教白富美加勒比久久|亚洲欧洲精品婷婷|日韩综合无码色色|日韩精品一区妖精视频|亚洲无码中文字幕hd|99亚洲思思丝袜|手机看片国产精品大胆亚洲|成人无码视频一区二区在线播放

【職位概述】
作為制造質(zhì)量團隊的核心成員，此崗位將主導(dǎo)產(chǎn)品全生命周期質(zhì)量管控，通過數(shù)據(jù)驅(qū)動的方法減少過程缺陷，確保符合GEHC等國際質(zhì)量體系標(biāo)準。該職位需協(xié)同全球供應(yīng)鏈團隊，具備跨文化溝通能力和技術(shù)決策能力。
【核心職責(zé)】
1. 質(zhì)量分析與改進
運用Minitab等工具進行缺陷數(shù)據(jù)統(tǒng)計分析，主導(dǎo)8D報告及CAPA制定
管理NCR/MRB流程，推動非符合物料庫存降低（目標(biāo)年降15%）
執(zhí)行SPC監(jiān)控，識別過程變異趨勢并聯(lián)動工藝工程師優(yōu)化
2. 跨職能協(xié)作
作為SQE與制造工程接口，主導(dǎo)供應(yīng)商質(zhì)量缺陷的根因分析
對接美國/印度工廠客戶，處理CT車間及醫(yī)院現(xiàn)場客訴（響應(yīng)時效≤24h）
維護DHR電子記錄系統(tǒng)，確保符合21 CFR Part 11合規(guī)要求
3. 體系運營
主導(dǎo)年度質(zhì)量內(nèi)審，推動ISO 13485體系落地
開發(fā)標(biāo)準化作業(yè)程序（SOP）并培訓(xùn)產(chǎn)線人員
【任職要求】
硬性條件
- 機械/機電工程專業(yè)，統(tǒng)招本科及以上學(xué)歷，3年以上相關(guān)經(jīng)驗
- 英語CET-6以上（口語流利可以熟練溝通）
技術(shù)能力
- 熟悉 APQP, FMEA, MSA, SPC, PPAP, CP 等質(zhì)量工具；
- 具備CPK/PPK分析經(jīng)驗
- 熟悉精益生產(chǎn)基礎(chǔ)
軟性素質(zhì)
- 能領(lǐng)導(dǎo)5-8人跨文化團隊
- 可同時管理3個以上質(zhì)量改進項目
- 可同時管理3個以上質(zhì)量改進項目
優(yōu)先條件
六西格瑪綠帶認證
汽車/醫(yī)療設(shè)備行業(yè)經(jīng)驗
具備供應(yīng)商審核經(jīng)驗（VDA6.3加分項）
專業(yè)路徑：高級質(zhì)量工程師→質(zhì)量經(jīng)理→質(zhì)量總監(jiān)
認證建議：優(yōu)先考取ASQ CQE或IRCA內(nèi)審員資格
Job Overview?
As a core member of the manufacturing quality team, you will lead end-to-end product quality control, leveraging data-driven methodologies to reduce process defects and ensure compliance with GEHC and other international quality standards. This role requires collaboration with global supply chain teams, cross-cultural communication skills, and technical decision-making capabilities.
?Key Responsibilities?
?1. Quality Analysis & Improvement?
Utilize Minitab for defect data analysis and lead 8D reports/CAPA development
Manage NCR/MRB processes, drive non-conforming material inventory reduction (15% annual target)
Implement SPC monitoring, identify process variation trends, and collaborate with process engineers for optimization
?2. Cross-functional Collaboration?
Serve as the interface between SQE and manufacturing engineering, leading root cause analysis of supplier quality defects
Liaise with US/India factory clients, addressing CT workshop and hospital site complaints (24-hour response SLA)
Maintain DHR electronic records to ensure 21 CFR Part 11 compliance
?3. System Operations?
Lead annual quality audits and drive ISO 13485 implementation
Develop SOPs and conduct training for production line personnel
?Qualifications?
?Category? ?Requirements?
?Hard Requirements? - Bachelor's in Mechanical/Electrical Engineering (or 3+ years experience + HS diploma)
- CET-6 English proficiency (fluent speaking)
?Technical Skills? - Proficient in GD&T/FMEA tools
- CPK/PPK analysis experience
- Lean manufacturing fundamentals
?Soft Skills? - Ability to lead 5-8-member cross-cultural teams
- Manage 3+ quality improvement projects concurrently
?Preferred Qualifications?
Six Sigma Green Belt certification
Automotive/medical device industry experience
Supplier audit experience (VDA6.3 preferred)
?Career Path?
?Technical Track?: Senior Quality Engineer → Quality Manager → Quality Director
?Certifications?: ASQ CQE or IRCA Auditor certification recommen