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AI CAPA Workflow Management Agent

CAPA workflow management tool for automotive manufacturing: automate RCA, risk scoring, and effectiveness checks
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Overview
Custom solution
Workflow

Automating CAPA Workflow Management with AI

Automate your complete CAPA workflow—from NCR intake and containment through root cause analysis, risk-based prioritization, corrective action tracking, and effectiveness verification.
001
Intelligent intake and risk triage

The Agent classifies incoming nonconformances, auto-links related events, triggers containment tasks, and assigns Action Priority based on AIAG/VDA severity, occurrence, and detection scores—escalating stop-ship decisions when risk warrants it.

002
AI-assisted root cause analysis

Pattern mining across SPC data, maintenance logs, supplier lot records, and machine alarms surfaces candidate causes, while a 5-Why copilot guides teams to verify both occurrence and escape causes with objective evidence.

003
Automated effectiveness verification

The system defines metrics, baselines, and acceptance thresholds for each corrective action—then monitors PPM, Cp/Cpk, SPC trends, and complaint rates over the verification window, blocking closure until criteria are met.

How Cassidy automates 8D / Nonconformance Response using AI

Step 1: Trigger on new nonconformance

The Workflow activates when an NCR, customer complaint, SCAR, or audit finding enters your QMS—whether from in-process inspection, end-of-line test, warranty return, or supplier escape.

Step 2: Classify and triage

Cassidy uses NLP to parse the defect description, auto-assign defect codes and suspected stations, link related events, and calculate an initial Action Priority score using AIAG/VDA logic. High-severity issues automatically trigger stop-ship holds in MES.

Step 3: Launch containment tasks

Based on defect type and severity, Cassidy generates a containment checklist—lot quarantine, 100% sort, rework instructions—and assigns tasks to the cross-functional 8D team with SLA-driven reminders.

Step 4: Guide root cause analysis

Cassidy pulls process parameters, SPC streams, maintenance logs, supplier CoAs, and prior 8D records into a unified view. Its 5-Why copilot proposes hypotheses, prompts for evidence, and ensures both occurrence and escape causes are addressed.

Step 5: Plan and approve corrective actions

The Workflow templates D6 tasks—process changes, Poka-Yoke, training, PFMEA/Control Plan updates—with owners, due dates, and e-signature approvals. Cassidy flags which FMEA entries need revision and drafts updated Action Priority assessments.

Step 6: Verify effectiveness

Cassidy builds a verification plan with defined metrics (PPM, Cp/Cpk, complaint rate), baselines, and pass/fail thresholds. It monitors production data over the effectiveness check window and alerts if metrics regress—preventing closure until all criteria are met.

Step 7: Close and propagate lessons learned

Once verification passes, Cassidy archives the complete 8D record with audit trail and e-signatures, pushes updates to PFMEA/Control Plans, and indexes the corrective action in the Knowledge Base so similar issues across products or processes can reuse proven fixes.

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A dedicated team to drive adoption and results

Our implementation experts work hands-on with your team to make sure you see real value - fast. From setup to optimization, we’re here to help every step of the way.

We enable your teams - no IT required

We train your builders, support their workflows, and make sure they get the most out of Cassidy without ever waiting on engineering.

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