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英语专业术语- 质量类(Quality)
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| 一、质量方面 |
| Accreditation Body:认可机构 |
| Accredited Laboratory:认可的实验室 |
| Active Part: 在用零件 |
| Active Part : 活动 |
| Aftermarket Parts:售后零件 |
| Analysis of Motion/Ergonomics:运动/人机工程学分析 |
| Approved Material:批准的材料 |
| Assessment:评定 |
| Audit:审核 |
| Benchmarking:基准确定 |
| Calibration:校准 |
| Capability:能力 |
| Capability Indices (CP CPK): 能力指数 |
| Certification Body/Registrar):认证机构 |
| Computer –Aided Design:计算机辅助设计 |
| Computer –Aided Design: 计算机辅助工程 |
| Consulting:咨询 |
| control plan(CP): 控制计划 |
| Corrective Action:纠正措施 |
| Corrective Action Plan:纠正措施计划 |
| Cost of Poor Quality:不良质量的成本 |
| Parts per million(PPM):每百万零件不合格数 |
| Performance Indices( PP\PPK):性能指数 |
| Preventive Action:预防措施 |
| Problem Solving:解决问题 |
| Procedures:程序 |
| Process Capability: 过程能力 |
| Process Flow Diagram( PFD):过程流程图 |
| Production Materials:生产用材料 |
| Quality Function Deployment( QFD): 质量功能展开 |
| Quality Manual(QM): 质量手册 |
| Quality Plan: 质量计划 |
| Quality Planning:质量策划 |
| Quality Records:质量记录 |
| Raw Data:原始数据 |
| Reaction Plan:反应计划 |
| Registered Suppliers/Subcontractors:注册的供方/分承包方 |
| Registrar: 注册机构 |
| Remote Location:外部场所 |
| Repair:返修 |
| Rework:返工 |
| Scope-Laboratory:范围—实验室 |
| Service Parts:维修零件 |
| Setup Verification:作业准备验证 |
| Automobile product confirmation :汽车供应链确认 |
| Customer special requirements :顾客特殊要求确认 |
| Business Plan / Quality Policy / Objective:经营计划/质量方针/目标 |
| Quality management system Planning :质量管理体系的策划 |
| Customer satisfaction / complaint :顾客满意监控及顾客投诉 |
| 12 months Performance Data Analysis & Review:绩效分析 |
| Continual Improvement :持续改进 |
| Following up last visit findings:跟进上次审核发现点 |
| Customer change status:客户变化情况 |
| Product Manufacturing Process:产品制造过程 |
| In-process inspection:制程检验 |
| Facility/Equipment/Tooling management Process:设施/设备/工具管理过程 |
| Identification and traceability process:标识和可追溯性过程 |
| Project management process:项目管理过程 |
| Customer special requirement :客户特殊要求 |
| Product approval process:产品批准过程 |
| Facility/Equipment/Tooling management Process :设施/设备/工具管理过程 |
| 2、Audit Team Interim Discussion and Daily Review 审核组讨论及当日小结 |
| Arrive Location to be audited到:达审核现场 |
| Working Lunch, Schedule Review and Audit Team Meeting:简单工作午餐及审核小组会议 |
| Cumlative Sum Charting(CUSUM):累积和图 |
| Design for Manufacturing(DFM):制造性设计 |
| Design of Experiments(DOE):试验设计 |
| Design Record:设计记录 |
| Documentation:文件 |
| Due Care: 应有的注意 |
| Enviroment:环境 |
| Failure Mode and Effects Analysis (FMEA):失效模式及后果分析 |
| Finite Element Analysis(FEA):有限元分析 |
| Functional Verification:功能验证 |
| Geometric Dimensioning&Tolerancing (GD&T):几何尺寸与公差 |
| Initial Process Study:初始过程研究 |
| Job Instructions:作业指导书: |
| Laboratory:实验室 |
| Laboratory Scope:实验室范围 |
| Last off Part Comparison:末件比较 |
| Layout Inspection:全尺寸检验 |
| Match Check:匹配检查 |
| Mistake Proofing:防错 |
| Muti-Disciplinary Approach:多方论证方法 |
| Nonconformance:不合格品 |
| Overall Equipment Effectiveness:设备总效率 |
| Simulation Techniques: 仿真技术 |
| Site:现场 |
| Solid Modeling:实体造型 |
| Special Characteristics:特殊特性 |
| Statistical Process Control:统计过程控制 |
| Subcontractors: 分承包方 |
| Subcontractor Development:分承包方的开发 |
| Supplier: 供方 |
| Suspect Material or Product:可疑的材料或产品 |
| Theory of Constraints:限制理论 |
| Tool:工具 |
| Validation:确认 |
| Value Added Production Process: 增值生产过程 |
| Value Analysis (VA):价值分析 |
| Value Engineering(VE): 价值工程 |
| Verification:验证 |
| 二、体系审核方面: |
| Arrive Location to be audited :到达审核现场 |
| Opening Meeting and Plant Tour: 首次会议及巡厂 |
| 1、Top Management / Management Representative高层/管理代表 |
| General Requirement / Organization Briefing :企业介绍 |
| Brief introduction of business / process flow :简略介绍公司的业务/工序流程 |
| Certificate Scope identify :认证范围确认 |
| Customer complaints management process: 顾客抱怨管理过程 |
| Continual Improvement :持续改进 |
| Data Analysis: 数据分析 |
| Corrective and Preventive Action: 纠正及预防措施 |
| Internal audit and management review: 内部审核及管理评审 |
| Document and Records Control Process:文件记录控制过程 |
| Human Resource Process:人力资源过程 |
| Summarize Audit Findings and Audit Team Meeting:审核总结及审核小组会议 |
| Closing Meeting : 末次会议 |