| name | control-plan |
| description | Control Plan — build, review, or audit a Prototype, Pre-launch, or Production Control Plan linked to PFMEA failure modes and controls. Use when creating a new control plan, updating after a process change or corrective action, or auditing an existing CP for completeness and PFMEA alignment. Covers AIAG Control Plan reference manual and IATF 16949 §8.5.1. |
| license | MIT |
| metadata | {"author":"RBraga01","version":"1.1","iso-9001":"8.5.1","iatf-16949":"8.5.1","aiag-reference":"AIAG Control Plan Reference Manual","domain":"quality-engineering","subdomain":"planning","industries":"automotive,electronics,aerospace,medical,general","status":"approved","created":"2026-06-06","last_updated":"2026-06-06","updated_by":"migmcc","reviewed_by":"RBraga01","standard_edition":"AIAG Control Plan Reference Manual (1995) / IATF 16949:2016 §8.5.1"} |
Control Plan
When to use
Use this skill when:
- Creating a new Control Plan for prototype, pre-launch, or production
- Reviewing an existing Control Plan for completeness and accuracy
- Updating the CP after a process change, corrective action (D7), or PFMEA update
- Auditing a supplier's Control Plan during qualification or an IATF audit
- Linking PFMEA controls to the Control Plan after FMEA review
Prerequisites
- Process Flow Diagram (required — CP must mirror the process flow sequence)
- PFMEA (required — CP controls derive from PFMEA recommended actions)
- Drawing with ballooned characteristics and tolerance data
- List of special and significant characteristics (SC, CC, KPC, KCC)
- MSA results for measurement systems referenced in the CP (for production CP)
Workflow
Step 1 — Determine the CP type
| Type | When | Purpose |
|---|
| Prototype | During prototype builds | Describes dimensional, material, and functional tests in prototype phase |
| Pre-launch | After prototype, before PPAP | Describes controls in place during pilot/pre-production runs |
| Production | After PPAP approval, at SOP | The living document — updated throughout product life |
All three types may coexist during APQP phases. The Production CP is the one submitted as PPAP Element 7.
Step 2 — Build the Control Plan structure
The CP is a table with one row per characteristic per process step. Each row contains:
Header section (document-level):
- Control Plan number and revision
- Part number and revision
- Part name / description
- Supplier / plant
- Supplier code (OEM code)
- Key contact / phone
- Core team (multi-functional)
- Date (original) and date (revised)
- Customer engineering approval (name/date) — if required
- Customer quality approval (name/date) — if required
- Supplier approval (name/date)
Detail columns (one row per characteristic):
| Column | What to enter |
|---|
| Part/process number | Reference number from Process Flow |
| Process name / operation description | Name of the process step |
| Machine, device, jig, or tool | Equipment used at this step |
| Number | Characteristic number (links to balloon drawing) |
| Product characteristic | Product feature being controlled (dimension, material property, appearance) |
| Process characteristic | Process parameter being controlled (temperature, pressure, speed, torque) |
| Special characteristic classification | SC, CC, KPC, KCC, *, ▲ per customer symbology |
| Product/process specification / tolerance | Nominal value and tolerance band |
| Evaluation / measurement technique | Gauge type, method, or test used |
| Sample size | Number of parts per sample |
| Frequency | How often samples are taken (every hour, every lot, 100%) |
| Control method | How the process is controlled (SPC chart, go/no-go gauge, visual, 100% inspection) |
| Reaction plan | What to do if out-of-control or out-of-specification (who, what action, containment) |
Step 3 — Populate from PFMEA
For each high-severity failure mode in the PFMEA:
- Identify the current prevention and detection controls from the PFMEA
- Transfer these controls into the corresponding CP row
- The reaction plan must address what happens if the control detects a non-conformance
Every special characteristic (SC, CC, ★, ◆) in the PFMEA must appear in the CP.
Every recommended action completed in the PFMEA must be reflected in the updated CP controls.
Step 4 — Special characteristics — mandatory coverage
| Classification | OEM symbol | CP requirement |
|---|
| Safety / Regulatory | ★ SC / ⬟ | 100% inspection OR demonstrated Cpk ≥ 1.67 + statistical monitoring |
| Critical Characteristic | CC / ◆ | Same as above — automatic stop if out of spec |
| Significant Characteristic | SC (Ford) / KPC | Process monitoring with defined sample plan and reaction |
| Key Control Characteristic | KCC | Process parameter monitoring (not product) — SPC or other control |
OEM symbol conventions vary. Always use the exact symbol specified in the customer's CSR:
- Ford: CC (Critical Characteristic) and SC (Significant Characteristic) — do not use ★ or ◆
- GM: ★ for safety-critical; Δ for significant
- VW / Audi: D (design feature, = CC), E (significant characteristic), I (functional dimension) per FORMEL Q
- BMW: G-SC (significant characteristic), G-CC (critical characteristic) per BMW standard
- Stellantis: CC and SC per MAQMSR — requires AIAG-VDA FMEA format alignment
Using the wrong symbol for the customer's OEM is an immediate finding at PPAP and IATF audit.
For all special characteristics: the reaction plan must specify who is notified, containment action, and when the process can restart.
Step 5 — Reaction plan requirements
Every row in the CP must have a reaction plan. Minimum requirements:
- Who is responsible for taking action
- What immediate containment is applied (tag, sort, hold, stop production)
- Who is notified (supervisor, quality, engineering)
- When production may restart (after what verification)
- Reference to relevant Work Instruction or SOP for the reaction
A reaction plan that says only "notify supervisor" or "quarantine parts" is insufficient — it must specify the next step after notification.
Step 6 — Audit an existing Control Plan
When reviewing a supplier's or internal CP, check:
Structure:
Characteristics:
Controls:
Reaction plan:
Alignment:
Validation criteria
A complete Production Control Plan for PPAP submission must:
- Cover every operation in the Process Flow
- Include every special and significant characteristic with correct classification
- Have a MSA-validated measurement system for every variable characteristic on SC/CC
- Have a reaction plan for every row
- Be signed by the APQP team (multi-functional) and have customer approval if required
- Match the PFMEA revision level
Common mistakes
- Control Plan created without reference to PFMEA — controls are generic, not linked to actual failure modes
- Reaction plan says "notify supervisor" only — not a reaction plan, just escalation
- Missing process characteristics — CP only controls product dimensions, not process parameters like temperature or torque
- Sample plan says "as required" — must specify a number and frequency
- SC/CC characteristics not identified with correct customer symbol — auditor will flag this immediately
- CP not updated after D7 of an 8D — the most common disconnect in corrective action systems
- Gauge type not specified — "visual inspection" or "measure" is not sufficient; must name the tool
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 | Added OEM-specific special characteristic symbol conventions (Ford, GM, VW, BMW, Stellantis) in Step 4 |