Supplier Auditor Training Program — Auditing the Machines™

Artificial Intelligence has quietly become part of everyday supplier operations — shaping documentation, quality analysis, process optimization, and even PFMEA and CAPA workflows. Yet most MedTech audit programs remain focused on traditional QMS controls and are not designed to detect unvalidated AI tools, cross-client data contamination, or invisible AI-assisted decisions.

NoioMed’s Supplier Auditor Training Program — Auditing the Machines™ closes this critical gap.

This online training equips experienced MedTech auditors with the AI literacy, risk-awareness, and practical audit techniques needed to evaluate suppliers who use AI in quality, design, analytics, and manufacturing environments. Built on NoioMed’s industry-leading frameworks for Responsible AI, this course teaches auditors how to identify hidden AI use, ask the right questions, and assess the governance controls necessary to protect IP, ensure compliance, and maintain supply-chain integrity.

What Auditors Will Learn

✓ How AI is being used (often invisibly) by suppliers

From CAPA summaries and PFMEA edits to predictive analytics and documentation drafting, auditors discover where AI is likely embedded in supplier workflows — even when not disclosed.

✓ The new risks AI introduces into supplier operations

Including cross-client data contamination, vector database leakage, prompt logging, unvalidated AI outputs, loss of traceability, and improper use of public AI platforms.

✓ How to expand supplier audits to include AI governance

Auditors gain a practical, structured approach to evaluating AI usage:
– What evidence to request
– What questions to ask engineers and quality teams
– How to recognize AI-assisted content
– How to assess data segregation and model validation
– When AI requires formal QMS controls

✓ How to integrate AI into supplier qualification and risk scoring

Including the use of AI Use Declarations, validation expectations, contractual updates, and the emerging regulatory landscape (FDA, QMSR, EU AI Act).

✓ How to future-proof audits for regulated industries

Auditors learn the foundational skills needed to evaluate AI systems as confidently as they evaluate CAPA, Document Control, or Design Controls today.

Who Should Attend

This program is designed for:
• Internal & external supplier auditors
• Supplier quality engineers (SQE)
• Quality & regulatory professionals
• Operations and engineering leaders involved in supplier oversight

Prior AI knowledge is not required.
Auditors only need strong existing QMS experience.

Course Format & Duration

This is a live, instructor-led online training hosted via NoioMed’s secure virtual learning environment.

Estimated Total Duration: 2.5 hours
– 2 hours of core training modules
– 30 minutes for live Q&A and applied case discussions

Participants receive:
• A downloadable AI-Audit Checklist
• A Supplier AI Use Declaration template
• A Certificate of Completion (digital)
• Optional add-ons for private team workshops

Why NoioMed?

NoioMed is at the forefront of Responsible AI adoption in regulated industries. Our frameworks, including AI With Integrity™, CP²T Tags, and CAPA360, help MedTech manufacturers integrate AI safely, effectively, and compliantly — without compromising IP protection or regulatory readiness.

This training distills the latest thinking from industry guidance, regulatory trends, and real supplier audit scenarios to give your auditors a decisive edge.

Prepare Your Audit Team for the Future of Supplier Oversight

AI will soon be part of every supplier’s workflow.
The question is whether your audit program is ready.

Equip your auditors to see what has always been invisible —
how the machines think, analyze, and remember.

→ Purchase the online training now
→ Group rates and corporate licensing available