VDA 6.3 Process Audit
When to use
Use this skill when:
- Conducting a VDA 6.3 process audit at a supplier or internally
- Preparing for an OEM process audit visit (BMW, VW, Audi, Mercedes, Porsche, Stellantis)
- Auditing a new supplier during qualification
- Responding to a customer concern by conducting a focused process audit
- Evaluating a supplier's manufacturing process capability before SOP
Prerequisites
- Customer audit scope (which process/product to audit)
- VDA 6.3 question catalogue (the auditor works from the standard questions)
- Process Flow Diagram, PFMEA, Control Plan, and Work Instructions for the audited process
- Access to the production area, equipment records, personnel, and quality records
Workflow
Step 1 — VDA 6.3 Structure Overview
VDA 6.3 is organised into 7 process elements (P1–P7):
| Element |
Name |
Applies to |
| P1 |
Potential Analysis |
New suppliers — evaluates readiness before series production |
| P2 |
Project Management |
APQP and product/process development process |
| P3 |
Planning the Product and Process Development |
Design and process planning activities |
| P4 |
Supplier Management (Purchasing) |
Sub-supplier control and qualification |
| P5 |
Process Input / Series |
Incoming materials and components |
| P6 |
Process Execution / Customer Satisfaction / Service |
The manufacturing process itself |
| P7 |
Customer Support / Customer Satisfaction / Service |
Delivery performance, escalation, field support |
For a focused series production audit (most common): P5, P6, P7 are mandatory. P1–P4 are added for new supplier qualification or product launch audits.
Step 2 — Rating system
Every question in VDA 6.3 is scored on a 0–10 scale:
| Score |
Meaning |
| 10 |
All requirements fulfilled — systematic, effective, and documented evidence exists |
| 8 |
Requirement largely fulfilled — minor gaps, no systematic risk |
| 6 |
Requirement partially fulfilled — deviations exist, limited risk |
| 4 |
Requirement insufficiently fulfilled — significant gaps, risk to quality |
| 2 |
Requirement not fulfilled — systematic failure, high risk |
| 0 |
Not applicable OR not fulfilled with no evidence |
A score of 4 or less on any question is a deficiency and must be documented with a finding and corrective action requirement.
Step 3 — Degree of Fulfillment calculation
For each process element:
Element score (%) = (Sum of all question scores) / (Maximum possible score) × 100
Weighting system (critical): Each question in the VDA 6.3 question catalogue has a pre-assigned weighting factor of 1, 2, or 3. These weights are fixed in the standard — the auditor cannot change them. Questions covering safety-critical topics (error-proofing, special characteristics control, non-conformance segregation) typically carry weight 2 or 3. The maximum possible score per question = 10 × weighting factor.
To calculate the degree of fulfillment correctly:
- Use the official VDA 6.3 question catalogue, which lists each question with its weight
- Sum (score × weight) for all applicable questions in the element
- Divide by the sum of (10 × weight) for all applicable questions
- Do not average raw scores — applying equal weight to all questions is a calculation error that produces incorrect element ratings
If a question is not applicable (N/A), it is excluded from both the numerator and denominator.
VDA 6.3 rating thresholds
| Degree of fulfillment |
Rating |
Interpretation |
| ≥ 90% |
A |
Process suitable for series production — no significant concerns |
| 75% – < 90% |
B |
Conditionally suitable — corrective actions required within agreed timeframe |
| < 75% |
C |
Not suitable — series production release blocked until corrective action complete |
A rating of C blocks SOP — the customer will not release the supplier for series production until re-audit achieves at least B.
Step 4 — P6 — Process Execution (the core audit)
P6 is the most extensive element and covers the actual manufacturing process. Key areas:
P6.1 — Process inputs
- Are incoming materials and components controlled?
- Are change management procedures in place and effective?
- Are specifications current and accessible at point of use?
P6.2 — Personnel
- Are operators qualified and trained for the tasks they perform?
- Are training records current?
- Is a qualification matrix maintained and used?
P6.3 — Resources (equipment, tools, gauges)
- Is equipment maintained per a preventive maintenance plan?
- Are calibration records current for all measurement equipment?
- Are work instructions present at every workstation and at the correct revision?
P6.4 — Failure mode prevention (error-proofing)
- Are poka-yoke devices in place for all High-AP failure modes?
- Are error-proofing devices checked at the correct frequency?
- Is the check result documented?
P6.5 — Quality inspections and tests
- Are incoming inspection, in-process inspection, and final inspection defined and performed?
- Are inspection records maintained and traceable?
- Is SPC in place for all special characteristics?
P6.6 — Non-conformance management
- Is non-conforming material identified, segregated, and controlled?
- Is there a defined reaction plan for out-of-control conditions?
- Are non-conformances escalated to quality and documented?
P6.7 — Continuous improvement
- Are quality KPIs tracked (reject rate, scrap, rework, OEE)?
- Are improvement actions driven by data?
- Are lessons learned captured and applied?
Step 5 — Conduct the audit
Pre-audit:
- Request all relevant documentation: Process Flow, PFMEA, Control Plan, WIs, maintenance records, calibration records, training records
- Review and identify gaps before the site visit
- Confirm auditor qualification: VDA 6.3 audits require a trained, qualified auditor — internal auditors must hold a recognised VDA 6.3 auditor qualification (VDA QMC certification or OEM-equivalent). An unqualified person conducting the audit invalidates the result.
- Confirm auditor independence: the auditor must not have direct responsibility for the process being audited. Self-assessment by the process owner is not a substitute for an independent audit.
Opening meeting:
- Confirm scope, timing, and audit plan
- Introduce audit team and request the process owner to accompany
Process walk (the audit):
- Follow the process flow physically — start from incoming material, end at shipment
- For each step: observe, ask, verify records
- Ask: "Show me the record for this" — never accept verbal confirmation
- Score each question in real time; document evidence (positive and negative)
Findings classification:
- Score 6: Partial fulfilment — finding documented, corrective action required; deadline typically 90 days
- Score 4: Insufficient fulfilment — significant gap, represents active risk to quality; escalate deadline; customer OEMs often treat score-4 findings on critical questions (P6.4, P6.5, P6.6) as major deficiencies requiring immediate corrective action
- Score 2: Not fulfilled — systematic failure, high risk; corrective action with accelerated timeline required before next delivery
- Score 0: No evidence / not implemented — blocking; re-audit required before SOP release (if P1 applicable)
Closing meeting:
- Present scores and degree of fulfillment per element
- Confirm overall rating (A, B, or C)
- Agree on corrective action deadlines (typically 90 days for B-rating findings; accelerated for score-2 and score-4 findings)
- For B rating: schedule a follow-up audit or evidence review within 3 months to verify corrective actions are implemented — do not close the audit without this commitment in writing
- Confirm re-audit requirements if applicable (mandatory for C rating)
Step 6 — Audit report structure
The VDA 6.3 report must contain:
- Audit information: date, location, auditor, auditee, scope
- Degree of fulfillment per element (P1–P7 as applicable)
- Overall rating (A, B, C)
- Finding list: for each score ≤ 6 — question, observation, evidence, score, deadline
- Positive findings: best practices worth noting
- Corrective action plan (CAP): supplier-signed, with root cause and due date per finding
- Re-audit requirement if C rating
Validation criteria
A VDA 6.3 audit is complete when:
- All applicable elements (P5, P6, P7 minimum for series) have been scored
- All findings (score ≤ 6) are documented with evidence
- Degree of fulfillment calculated and overall rating stated
- Corrective action plan signed by supplier quality management
- Re-audit scheduled if rating is C
Common mistakes
- Auditor accepts verbal confirmation as evidence — always request the record
- Skipping the process walk and only reviewing documents — P6 requires observation of the live process
- Not documenting positive evidence — the report must balance findings and strengths
- Calculating degree of fulfillment without applying question weights
- Not confirming error-proofing device checks are being performed at the required frequency
- Closing meeting without confirming the corrective action deadline in writing
- Rating B without scheduling a follow-up to verify corrective actions are implemented
Output Format
At the start of each use, ask the user:
"How would you like to receive the output?
A — Structured Markdown (formatted tables and sections, ready to copy)
B — Plain tables (simplified structure for Excel or Word)
C — Narrative report (flowing text for a formal document or email)
Default: A."
Adapt all output sections to the chosen format. If the platform or session context already defines a format preference, skip this question.
Changelog
| Version |
Date |
Author |
Change |
| 1.0 |
2026-06-06 |
@RBraga01 |
Initial release |
| 1.1 |
2026-06-06 |
@migmcc |
Expanded weighting system explanation in Step 3; added auditor qualification and independence requirements; improved findings classification (score 4 vs 6 distinction); added B-rating follow-up timeline |
Source: hashgraph-online/awesome-codex-plugins → plugins/RBraga01/Quality-Engineering-Skills/skills/audit/vda-6-3-audit/SKILL.md
1---2name: vda-6-3-audit3description: >- VDA 6.3 Process Audit — conduct or prepare for a process audit using the VDA 6.3 methodology, evaluate process elements P1–P7, calculate degree of fulfillment, classify findings, and generate an audit report. Use when a customer requests a VDA 6.3 audit, when auditing a supplier's manufacturing process, or when preparing for a VDA process audit visit. Covers VDA 6.3 4th edition (2023).4---567# VDA 6.3 Process Audit89## When to use1011Use this skill when:12- Conducting a VDA 6.3 process audit at a supplier or internally13- Preparing for an OEM process audit visit (BMW, VW, Audi, Mercedes, Porsche, Stellantis)14- Auditing a new supplier during qualification15- Responding to a customer concern by conducting a focused process audit16- Evaluating a supplier's manufacturing process capability before SOP1718## Prerequisites1920- Customer audit scope (which process/product to audit)21- VDA 6.3 question catalogue (the auditor works from the standard questions)22- Process Flow Diagram, PFMEA, Control Plan, and Work Instructions for the audited process23- Access to the production area, equipment records, personnel, and quality records2425## Workflow2627### Step 1 — VDA 6.3 Structure Overview2829VDA 6.3 is organised into 7 process elements (P1–P7):3031| Element | Name | Applies to |32|---------|------|-----------|33| P1 | Potential Analysis | New suppliers — evaluates readiness before series production |34| P2 | Project Management | APQP and product/process development process |35| P3 | Planning the Product and Process Development | Design and process planning activities |36| P4 | Supplier Management (Purchasing) | Sub-supplier control and qualification |37| P5 | Process Input / Series | Incoming materials and components |38| P6 | Process Execution / Customer Satisfaction / Service | The manufacturing process itself |39| P7 | Customer Support / Customer Satisfaction / Service | Delivery performance, escalation, field support |4041**For a focused series production audit (most common):** P5, P6, P7 are mandatory. P1–P4 are added for new supplier qualification or product launch audits.4243---4445### Step 2 — Rating system4647Every question in VDA 6.3 is scored on a 0–10 scale:4849| Score | Meaning |50|-------|---------|51| **10** | All requirements fulfilled — systematic, effective, and documented evidence exists |52| **8** | Requirement largely fulfilled — minor gaps, no systematic risk |53| **6** | Requirement partially fulfilled — deviations exist, limited risk |54| **4** | Requirement insufficiently fulfilled — significant gaps, risk to quality |55| **2** | Requirement not fulfilled — systematic failure, high risk |56| **0** | Not applicable OR not fulfilled with no evidence |5758A score of **4 or less** on any question is a deficiency and must be documented with a finding and corrective action requirement.5960---6162### Step 3 — Degree of Fulfillment calculation6364For each process element:6566**Element score (%) = (Sum of all question scores) / (Maximum possible score) × 100**6768**Weighting system (critical):** Each question in the VDA 6.3 question catalogue has a pre-assigned weighting factor of 1, 2, or 3. These weights are fixed in the standard — the auditor cannot change them. Questions covering safety-critical topics (error-proofing, special characteristics control, non-conformance segregation) typically carry weight 2 or 3. The maximum possible score per question = 10 × weighting factor.6970To calculate the degree of fulfillment correctly:71- Use the official VDA 6.3 question catalogue, which lists each question with its weight72- Sum (score × weight) for all applicable questions in the element73- Divide by the sum of (10 × weight) for all applicable questions74- Do not average raw scores — applying equal weight to all questions is a calculation error that produces incorrect element ratings7576If a question is not applicable (N/A), it is excluded from both the numerator and denominator.7778#### VDA 6.3 rating thresholds7980| Degree of fulfillment | Rating | Interpretation |81|----------------------|--------|----------------|82| ≥ 90% | A | Process suitable for series production — no significant concerns |83| 75% – < 90% | B | Conditionally suitable — corrective actions required within agreed timeframe |84| < 75% | C | Not suitable — series production release blocked until corrective action complete |8586A rating of **C blocks SOP** — the customer will not release the supplier for series production until re-audit achieves at least B.8788---8990### Step 4 — P6 — Process Execution (the core audit)9192P6 is the most extensive element and covers the actual manufacturing process. Key areas:9394**P6.1 — Process inputs**95- Are incoming materials and components controlled?96- Are change management procedures in place and effective?97- Are specifications current and accessible at point of use?9899**P6.2 — Personnel**100- Are operators qualified and trained for the tasks they perform?101- Are training records current?102- Is a qualification matrix maintained and used?103104**P6.3 — Resources (equipment, tools, gauges)**105- Is equipment maintained per a preventive maintenance plan?106- Are calibration records current for all measurement equipment?107- Are work instructions present at every workstation and at the correct revision?108109**P6.4 — Failure mode prevention (error-proofing)**110- Are poka-yoke devices in place for all High-AP failure modes?111- Are error-proofing devices checked at the correct frequency?112- Is the check result documented?113114**P6.5 — Quality inspections and tests**115- Are incoming inspection, in-process inspection, and final inspection defined and performed?116- Are inspection records maintained and traceable?117- Is SPC in place for all special characteristics?118119**P6.6 — Non-conformance management**120- Is non-conforming material identified, segregated, and controlled?121- Is there a defined reaction plan for out-of-control conditions?122- Are non-conformances escalated to quality and documented?123124**P6.7 — Continuous improvement**125- Are quality KPIs tracked (reject rate, scrap, rework, OEE)?126- Are improvement actions driven by data?127- Are lessons learned captured and applied?128129---130131### Step 5 — Conduct the audit132133**Pre-audit:**134- Request all relevant documentation: Process Flow, PFMEA, Control Plan, WIs, maintenance records, calibration records, training records135- Review and identify gaps before the site visit136- Confirm auditor qualification: VDA 6.3 audits require a trained, qualified auditor — internal auditors must hold a recognised VDA 6.3 auditor qualification (VDA QMC certification or OEM-equivalent). An unqualified person conducting the audit invalidates the result.137- Confirm auditor independence: the auditor must not have direct responsibility for the process being audited. Self-assessment by the process owner is not a substitute for an independent audit.138139**Opening meeting:**140- Confirm scope, timing, and audit plan141- Introduce audit team and request the process owner to accompany142143**Process walk (the audit):**144- Follow the process flow physically — start from incoming material, end at shipment145- For each step: observe, ask, verify records146- Ask: "Show me the record for this" — never accept verbal confirmation147- Score each question in real time; document evidence (positive and negative)148149**Findings classification:**150- **Score 6:** Partial fulfilment — finding documented, corrective action required; deadline typically 90 days151- **Score 4:** Insufficient fulfilment — significant gap, represents active risk to quality; escalate deadline; customer OEMs often treat score-4 findings on critical questions (P6.4, P6.5, P6.6) as major deficiencies requiring immediate corrective action152- **Score 2:** Not fulfilled — systematic failure, high risk; corrective action with accelerated timeline required before next delivery153- **Score 0:** No evidence / not implemented — blocking; re-audit required before SOP release (if P1 applicable)154155**Closing meeting:**156- Present scores and degree of fulfillment per element157- Confirm overall rating (A, B, or C)158- Agree on corrective action deadlines (typically 90 days for B-rating findings; accelerated for score-2 and score-4 findings)159- For B rating: schedule a follow-up audit or evidence review within 3 months to verify corrective actions are implemented — do not close the audit without this commitment in writing160- Confirm re-audit requirements if applicable (mandatory for C rating)161162---163164### Step 6 — Audit report structure165166The VDA 6.3 report must contain:1671681. Audit information: date, location, auditor, auditee, scope1692. Degree of fulfillment per element (P1–P7 as applicable)1703. Overall rating (A, B, C)1714. Finding list: for each score ≤ 6 — question, observation, evidence, score, deadline1725. Positive findings: best practices worth noting1736. Corrective action plan (CAP): supplier-signed, with root cause and due date per finding1747. Re-audit requirement if C rating175176---177178## Validation criteria179180A VDA 6.3 audit is complete when:181- All applicable elements (P5, P6, P7 minimum for series) have been scored182- All findings (score ≤ 6) are documented with evidence183- Degree of fulfillment calculated and overall rating stated184- Corrective action plan signed by supplier quality management185- Re-audit scheduled if rating is C186187## Common mistakes188189- Auditor accepts verbal confirmation as evidence — always request the record190- Skipping the process walk and only reviewing documents — P6 requires observation of the live process191- Not documenting positive evidence — the report must balance findings and strengths192- Calculating degree of fulfillment without applying question weights193- Not confirming error-proofing device checks are being performed at the required frequency194- Closing meeting without confirming the corrective action deadline in writing195- Rating B without scheduling a follow-up to verify corrective actions are implemented196197## Output Format198199At the start of each use, ask the user:200201> "How would you like to receive the output?202> **A** — Structured Markdown (formatted tables and sections, ready to copy)203> **B** — Plain tables (simplified structure for Excel or Word)204> **C** — Narrative report (flowing text for a formal document or email)205>206> Default: A."207208Adapt all output sections to the chosen format. If the platform or session context already defines a format preference, skip this question.209210## Changelog211212| Version | Date | Author | Change |213|---------|------|--------|--------|214| 1.0 | 2026-06-06 | @RBraga01 | Initial release |215| 1.1 | 2026-06-06 | @migmcc | Expanded weighting system explanation in Step 3; added auditor qualification and independence requirements; improved findings classification (score 4 vs 6 distinction); added B-rating follow-up timeline |216217---218219**Source:** [`hashgraph-online/awesome-codex-plugins`](https://github.com/hashgraph-online/awesome-codex-plugins) → `plugins/RBraga01/Quality-Engineering-Skills/skills/audit/vda-6-3-audit/SKILL.md`