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[size=1em] 规划(Plan)——供应商开发与准入
[size=1em](1)明确采购需求
[size=1em]产品/服务规格(技术参数、质量标准
[size=1em]供应商准入标准
[size=1em]资质 营业执照、行业认证(ISO9001、IATF16949、ISO13485等)
[size=1em]质量能力 质量体系、检测设备、过程控制能力(SPC、FMEA)
[size=1em]交付能力 产能、交货准时率、应急响应
[size=1em]成本竞争力 报价合理性、降本潜力
[size=1em]服务与配合度 沟通效率、问题响应速度
[size=1em]可持续性 环保合规、社会责任、ESG表现
[size=1em]现场审核(On-site Audit)
[size=1em]质量体系审核(QSA)
[size=1em]制造过程审核(如VDA6.3)
[size=1em]仓储与物流能力检查
[size=1em]📌 输出:《供应商审核报告》《准入审批表》
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[size=1em]2. 实施(Do)——合作与订单执行
[size=1em](1)签订协议
[size=1em]采购合同
[size=1em]质量协议(Quality Agreement)
[size=1em]保密协议(NDA)
[size=1em]SOP(标准操作程序)
[size=1em](2)小批量试产(PPAP)
[size=1em]样品确认(FAI:首件检验)
[size=1em]提交PPAP文件(生产件批准程序),常见等级3:
[size=1em]PSW(零件提交保证书)
[size=1em]FMEA、控制计划、MSA、SPC报告
[size=1em]全尺寸报告、材料证明
[size=1em](3)批量供货
[size=1em]下达采购订单(PO)
[size=1em]跟踪生产进度与物流状态
[size=1em]执行IQC(来料检验)
[size=1em]3. 检查(Check)——绩效评估与监控
[size=1em]建立KPI指标体系(月度/季度评估)
[size=1em]4. 改进(Act)——持续优化与协同
[size=1em](1)问题处理(CAPA)
[size=1em]发出《8D报告》或《纠正预防措施单》
[size=1em]跟踪根本原因分析与整改措施落地
[size=1em]验证有效性(如复检、过程验证)
[size=1em](2)联合改进项目
[size=1em]成本优化(VA/VE:价值分析/价值工程)
[size=1em]质量提升(六西格玛、精益改善)
[size=1em]交付协同(VMI、JIT、CPFR)
[size=1em]5. 淘汰与更新(Close & Renew)
[size=1em]对长期绩效差(C/D级)的供应商启动淘汰流程
[size=1em]引入备选供应商,建立合格供应商名录(AVL / Approved Vendor List)
[size=1em]定期更新供应商库,保持竞争与活力
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Plan - Supplier Development and Access
(1) Clarify procurement requirements
Product/service specifications (technical parameters, quality standards)
Supplier admission criteria
Qualification Business License, Industry Certification (ISO9001, IATF16949, ISO13485, etc.)
Quality Capability Quality System, Testing Equipment, Process Control Capability (SPC, FMEA)
Delivery capacity, on-time delivery rate, emergency response
Cost competitiveness, reasonable pricing, and potential for cost reduction
Service and cooperation, communication efficiency, and problem response speed
Sustainability, environmental compliance, social responsibility, ESG performance
On site Audit
Quality System Audit (QSA)
Manufacturing process audit (such as VDA6.3)
Warehouse and logistics capacity inspection
📌 Output: Supplier Audit Report and Admission Approval Form
2. Implementation (Do) - Collaboration and Order Execution
(1) Sign the agreement
purchase contract
Quality Agreement
Confidentiality Agreement (NDA)
SOP (Standard Operating Procedure)
(2) Small Batch Trial Production (PPAP)
Sample Confirmation (FAI: First Article Inspection)
Submit PPAP documents (Production Part Approval Procedure), common level 3:
PSW (Parts Submission Guarantee)
FMEA、 Control plan, MSA, SPC report
Full size report, material proof
(3) Batch supply
Place a Purchase Order (PO)
Track production progress and logistics status
Execute IQC (Incoming Inspection)
3. Check - Performance Evaluation and Monitoring
Establish KPI indicator system (monthly/quarterly evaluation)
4. Improvement (Act) - Continuous Optimization and Collaboration
(1) Problem Handling (CAPA)
Issue the 8D Report or Corrective and Preventive Action Form
Track root cause analysis and implementation of corrective measures
Validity verification (such as retesting, process validation)
(2) Joint improvement project
Cost optimization (VA/VE: Value Analysis/Value Engineering)
Quality improvement (Six Sigma, Lean Improvement)
Delivery collaboration (VMI, JIT, CPFR)
5. Close&Renew
Initiate elimination process for suppliers with long-term poor performance (C/D level)
Introduce alternative suppliers and establish a qualified supplier list (AVL/Approved Vendor List)
Regularly update the supplier database to maintain competition and vitality
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