---

name: qms-audit-expert description: > ISO 13485 internal audit expertise for medical device QMS. Use for audit planning and execution, nonconformity classification, CAPA verification, external audit preparation, or audit program management. license: MIT + Commons Clause metadata: version: 1.0.0 author: borghei category: compliance domain: quality-audit updated: 2026-03-31 tags: [iso-13485, audit, nonconformity, quality-audit, certification]

QMS Audit Expert

ISO 13485 internal audit methodology for medical device quality management systems.

---

Table of Contents

• Audit Planning Workflow
• Audit Execution
• Nonconformity Management
• External Audit Preparation
• Reference Documentation
• Tools

---

Clarify First

Before planning or executing the audit, confirm these inputs. If any is unknown or vague, ASK — do not assume:

• Audit purpose — internal scheduled audit, external/certification prep, or mock audit (sets the scope and formality)
• Processes/clauses in scope — which ISO 13485 clauses (drives the checklist and frequency)
• Risk level and prior findings per process — picks audit frequency and sample size

Stop rule: ask only the 2-3 that most change the output. If the user says "just draft it," proceed and list your assumptions at the top of the audit plan.

Audit Planning Workflow

Plan risk-based internal audit program:

1. List all QMS processes requiring audit
2. Assign risk level to each process (High/Medium/Low)
3. Review previous audit findings and trends
4. Determine audit frequency by risk level
5. Assign qualified auditors (verify independence)
6. Create annual audit schedule
7. Communicate schedule to process owners
8. Validation: All ISO 13485 clauses covered within cycle

Risk-Based Audit Frequency

Risk Level	Frequency	Criteria
High	Quarterly	Design control, CAPA, production validation
Medium	Semi-annual	Purchasing, training, document control
Low	Annual	Infrastructure, management review (if stable)

Audit Scope by Clause

Clause	Process	Focus Areas
4.2	Document Control	Document approval, distribution, obsolete control
5.6	Management Review	Inputs complete, decisions documented, actions tracked
6.2	Training	Competency defined, records complete, effectiveness verified
7.3	Design Control	Inputs, reviews, V&V, transfer, changes
7.4	Purchasing	Supplier evaluation, incoming inspection
7.5	Production	Work instructions, process validation, DHR
7.6	Calibration	Equipment list, calibration status, out-of-tolerance
8.2.2	Internal Audit	Schedule compliance, auditor independence
8.3	NC Product	Identification, segregation, disposition
8.5	CAPA	Root cause, implementation, effectiveness

Auditor Independence

Verify auditor independence before assignment:

• Auditor not responsible for area being audited
• No direct reporting relationship to auditee
• Not involved in recent activities under audit
• Documented qualification for audit scope

---

Audit Execution

Conduct systematic internal audit:

1. Prepare audit plan (scope, criteria, schedule)
2. Review relevant documentation before audit
3. Conduct opening meeting with auditee
4. Collect evidence (records, interviews, observation)
5. Classify findings (Major/Minor/Observation)
6. Conduct closing meeting with preliminary findings
7. Prepare audit report within 5 business days
8. Validation: All scope items covered, findings supported by evidence

Evidence Collection

Method	Use For	Documentation
Document review	Procedures, records	Document number, version, date
Interview	Process understanding	Interviewee name, role, summary
Observation	Actual practice	What, where, when observed
Record trace	Process flow	Record IDs, dates, linkage

Audit Questions by Clause

Document Control (4.2):

• Show me the document master list
• How do you control obsolete documents?
• Show me evidence of document change approval

Design Control (7.3):

• Show me the Design History File for [product]
• Who participates in design reviews?
• Show me design input to output traceability

CAPA (8.5):

• Show me the CAPA log with open items
• How do you determine root cause?
• Show me effectiveness verification records

See references/iso13485-audit-guide.md for complete question sets.

Finding Documentation

Document each finding with:

Requirement: [Specific ISO 13485 clause or procedure]
Evidence: [What was observed, reviewed, or heard]
Gap: [How evidence fails to meet requirement]

Example:

Requirement: ISO 13485:2016 Clause 7.6 requires calibration
at specified intervals.

Evidence: Calibration records for pH meter (EQ-042) show
last calibration 2024-01-15. Calibration interval is
12 months. Today is 2025-03-20.

Gap: Equipment is 2 months overdue for calibration,
representing a gap in calibration program execution.

---

Nonconformity Management

Classify and manage audit findings:

1. Evaluate finding against classification criteria
2. Assign severity (Major/Minor/Observation)
3. Document finding with objective evidence
4. Communicate to process owner
5. Initiate CAPA for Major/Minor findings
6. Track to closure
7. Verify effectiveness at follow-up
8. Validation: Finding closed only after effective CAPA

Classification Criteria

Category	Definition	CAPA Required	Timeline
Major	Systematic failure or absence of element	Yes	30 days
Minor	Isolated lapse or partial implementation	Recommended	60 days
Observation	Improvement opportunity	Optional	As appropriate

Classification Decision

Is required element absent or failed?
├── Yes → Systematic (multiple instances)? → MAJOR
│   └── No → Could affect product safety? → MAJOR
│       └── No → MINOR
└── No → Deviation from procedure?
    ├── Yes → Recurring? → MAJOR
    │   └── No → MINOR
    └── No → Improvement opportunity? → OBSERVATION

CAPA Integration

Finding Severity	CAPA Depth	Verification
Major	Full root cause analysis (5-Why, Fishbone)	Next audit or within 6 months
Minor	Immediate cause identification	Next scheduled audit
Observation	Not required	Noted at next audit

See references/nonconformity-classification.md for detailed guidance.

---

External Audit Preparation

Prepare for certification body or regulatory audit:

1. Complete all scheduled internal audits
2. Verify all findings closed with effective CAPA
3. Review documentation for currency and accuracy
4. Conduct management review with audit as input
5. Prepare facility and personnel
6. Conduct mock audit (full scope)
7. Brief personnel on audit protocol
8. Validation: Mock audit findings addressed before external audit

Pre-Audit Readiness Checklist

Documentation:

• Quality Manual current
• Procedures reflect actual practice
• Records complete and retrievable
• Previous audit findings closed

Personnel:

• Key personnel available during audit
• Subject matter experts identified
• Personnel briefed on audit protocol
• Escorts assigned

Facility:

• Work areas organized
• Documents at point of use current
• Equipment calibration status visible
• Nonconforming product segregated

Mock Audit Protocol

1. Use external auditor or qualified internal auditor
2. Cover full scope of upcoming external audit
3. Simulate actual audit conditions (timing, formality)
4. Document findings as for real audit
5. Address all Major and Minor findings before external audit
6. Brief management on readiness status

---

Reference Documentation

ISO 13485 Audit Guide

references/iso13485-audit-guide.md contains:

• Clause-by-clause audit methodology
• Sample audit questions for each clause
• Evidence collection requirements
• Common nonconformities by clause
• Finding severity classification

Nonconformity Classification

references/nonconformity-classification.md contains:

• Severity classification criteria and decision tree
• Impact vs. occurrence matrix
• CAPA integration requirements
• Finding documentation templates
• Closure requirements by severity

---

Tools

Audit Schedule Optimizer

# Generate optimized audit schedule
python scripts/audit_schedule_optimizer.py --processes processes.json

# Interactive mode
python scripts/audit_schedule_optimizer.py --interactive

# JSON output for integration
python scripts/audit_schedule_optimizer.py --processes processes.json --output json

Generates risk-based audit schedule considering:

• Process risk level
• Previous findings
• Days since last audit
• Criticality scores

Output includes:

• Prioritized audit schedule
• Quarterly distribution
• Overdue audit alerts
• Resource recommendations

Sample Process Input

{
  "processes": [
    {
      "name": "Design Control",
      "iso_clause": "7.3",
      "risk_level": "HIGH",
      "last_audit_date": "2024-06-15",
      "previous_findings": 2
    },
    {
      "name": "Document Control",
      "iso_clause": "4.2",
      "risk_level": "MEDIUM",
      "last_audit_date": "2024-09-01",
      "previous_findings": 0
    }
  ]
}

---

Audit Program Metrics

Track audit program effectiveness:

Metric	Target	Measurement
Schedule compliance	>90%	Audits completed on time
Finding closure rate	>95%	Findings closed by due date
Repeat findings	<10%	Same finding in consecutive audits
CAPA effectiveness	>90%	Verified effective at follow-up
Auditor utilization	4 days/month	Audit days per qualified auditor

---

Troubleshooting

Problem	Likely Cause	Resolution
Schedule optimizer produces no audits for a process	last_audit_date is recent and risk level is Low	Low-risk processes are scheduled annually. If the last audit was within 365 days, no new audit is generated. Increase risk_level or criticality_score to trigger earlier scheduling.
Optimizer flags all processes as overdue	Date format in processes.json is incorrect	Use ISO 8601 format (YYYY-MM-DD) for last_audit_date. Invalid dates cause the tool to treat the last audit as missing.
Interactive mode does not accept input	Terminal does not support stdin prompts	Use file-based input with --processes processes.json instead of --interactive.
Audit schedule does not cover all ISO 13485 clauses	Input process list is incomplete	The optimizer schedules only the processes provided. Ensure all required clauses (4.2, 5.6, 6.2, 7.3, 7.4, 7.5, 7.6, 8.2.2, 8.3, 8.5) are represented in the input.
Finding classified as Minor but should be Major	Classification was applied inconsistently	Apply the decision tree: systematic failure or absent element = Major; isolated lapse = Minor. Consider whether the finding could affect product safety (auto-escalate to Major).
External auditor raises finding already closed internally	CAPA effectiveness verification not completed before external audit	Ensure all internal audit findings have completed CAPA with documented effectiveness verification before the external audit date. Close the loop, do not just complete the action.
Audit report rejected by process owner	Findings not supported by objective evidence	Every finding must reference specific evidence (document number, record ID, observation details). Rework findings using the Requirement-Evidence-Gap format documented in this skill.

---

Success Criteria

• Annual audit schedule covers 100% of ISO 13485 clauses with risk-based frequency (quarterly for high-risk, semi-annual for medium, annual for low)
• Schedule compliance rate exceeds 90% (audits completed on time vs. planned)
• All Major findings result in full root cause analysis CAPA initiated within 30 days and verified effective within 6 months
• Finding closure rate exceeds 95% by due date, with no overdue Major findings at any point
• Repeat finding rate below 10% across consecutive audit cycles, demonstrating effective corrective actions
• Auditor independence verified and documented for every audit assignment (no self-auditing of own work area)
• Mock audit conducted before every external certification or surveillance audit with all Major and Minor findings resolved

---

Scope & Limitations

In Scope:

• ISO 13485:2016 internal audit planning, scheduling, and execution
• Risk-based audit frequency optimization
• Nonconformity classification (Major/Minor/Observation) with decision tree
• CAPA integration for audit findings
• External audit preparation and mock audit protocols
• Audit program metrics and effectiveness tracking

Out of Scope:

• External audit execution (this skill supports preparation for and response to external audits, not conducting them)
• Regulatory inspection management (FDA, Notified Body inspections have jurisdiction-specific protocols beyond internal audit scope)
• Detailed CAPA root cause analysis methodology (use capa-officer skill for 5-Why, Fishbone, FTA, FMEA)
• ISO 19011 auditor certification or training program administration
• Technical product testing or process validation
• QMSR-specific audit checklist generation (use quality-manager-qms-iso13485 for QMSR gap analysis)

---

Integration Points

Skill	Integration
quality-manager-qms-iso13485	Provides the QMS process framework that the audit program evaluates; audit results feed into management review inputs
capa-officer	Major and Minor audit findings trigger CAPA initiation; CAPA effectiveness verification closes the audit finding loop
quality-documentation-manager	Document control audit coverage (Clause 4.2) validates document numbering, approval workflows, and Part 11 compliance
quality-manager-qmr	Audit program results are a required management review input (Clause 5.6.2); QMR oversees audit program effectiveness
risk-management-specialist	Risk management process audit (Clause 7.1) verifies ISO 14971 implementation and risk file completeness

---

Tool Reference

audit_schedule_optimizer.py

Generates risk-based audit schedules optimized by process risk, findings history, and time since last audit.

Flag	Required	Description
--processes	Yes (or --interactive)	Path to JSON file containing process definitions with name, iso_clause, risk_level (HIGH/MEDIUM/LOW), last_audit_date, previous_findings, and criticality_score
--interactive	No	Launch interactive mode for guided process entry (alternative to file input)
--output	No	Output format: json for structured output, omit for human-readable text