
Your suppliers should be an asset, not a liability. We help manufacturers reduce supplier defects by 40-60%, cut scrap costs by $780K+, and build audit-ready compliance — backed by 30+ years of OEM SQE leadership and the ExceleorQMS digital platform.
From audits to PPAP packages to regulatory readiness — every engagement is designed to deliver measurable ROI and funnel into ongoing quality improvement.
Trust-Building Entry Point
Professional on-site and remote assessments conducted by former OEM Lead Auditors with insider audit perspective. We don't just read standards — we enforce them.
Proven 40-60% Reduction in 90 Days
Data-driven root cause analysis and corrective action methods that eliminate supplier-caused scrap at the source. Our programs identify the top 5 suppliers causing 80% of your scrap.
Production Part Approval — Done Right
Complete PPAP documentation packages prepared by certified quality engineers. We handle the entire 18-element PPAP submission so your team can focus on production — not paperwork.
FDA QMSR Is Effective NOW — Are You Ready?
The FDA's Quality Management System Regulation is already in effect, giving inspectors authority to review supplier audit reports, internal quality audits, and management reviews. We prepare you for inspection readiness.
High-Barrier Niche. Few Can Match.
Supplier quality compliance for defense contractors with security-cleared personnel. We navigate the complexity of federal acquisition regulations so you can focus on delivering to the warfighter.
Proactive Risk Detection — Not Reactive Crisis
Risk-based supplier evaluation using our proprietary 6-dimension assessment framework. Identify at-risk suppliers before they become supply chain disruptions — because 69% of CEOs cite supplier disruption as a primary concern.
Scrap reduction engagement that identified 5 suppliers responsible for 80% of quality escapes. Implemented SCAR process with full accountability tracking.
Production Part Approval Process documentation is where contracts are won or lost. Our certified quality engineers prepare complete 18-element PPAP packages with a 100% first-submission approval rate — so your team can focus on production, not paperwork.
Our auditors hold active certifications across all major quality standards. We don't generalize — we specialize in the verticals driving supplier quality demand.
AS9100, NADCAP, DFARS, ITAR
IATF 16949, PPAP, APQP, VDA
ISO 13485, FDA QMSR, EU MDR
ISO 9001, Lean, Six Sigma
Every consulting engagement is a funnel into ExceleorQMS. Every ExceleorQMS deployment generates data that justifies deeper consulting. This is the compounding flywheel.
Automated supplier performance dashboards with real-time data, auto-escalation, and trend analytics. Cuts manual data-entry errors by 90%.
Learn MoreMobile field auditing, customizable checklists, closed-loop CAPA tracking, and immutable digital audit trails. ROI within 6-12 months.
Learn MoreTemplated PPAP package builder with auto-populated forms, dimensional report integration, and customer-specific formatting. Submit with confidence.
Learn MoreProfessional-grade SCAR templates, audit checklists, supplier scorecards, incoming inspection forms, and APQP/PPAP documentation kits.
Learn MoreUnlike generalist consultancies that lack vertical depth or enterprise software vendors that sell tools without operational judgment — we deliver both.
Not consultants who read standards — auditors who enforce them. We bring the insider OEM audit perspective.
$1.85B in managed assets, 43,000+ component SKUs. Real operational experience at Fortune 500 scale.
Security-cleared personnel for DFARS, ITAR, and classified defense supplier quality work.
Seamless handoff to ISO consulting, EHS auditing, Lean Six Sigma, training, and fractional leadership across the Exceleor family.
In a market where competitors hide pricing, we publish ours. No hidden fees, no surprises.
Our digital quality platform sustains the gains — right-sized for SMEs that Tier 1 platforms over-serve.
Common questions about our supplier quality services
We serve aerospace & defense (AS9100, NADCAP, DFARS), automotive (IATF 16949, PPAP), medical devices (ISO 13485, FDA QMSR), and general manufacturing (ISO 9001). Our auditors hold active certifications across all major standards.
Our scrap reduction programs typically deliver 40-60% reduction within 90 days. In a recent engagement, we reduced an automotive Tier 2 supplier's scrap from $87K/month to $22K/month — a $780K annual savings.
We prepare complete PPAP packages covering all 18 elements per AIAG PPAP 4th Edition, including design records, control plans, PFMEAs, process flow diagrams, dimensional results, material certifications, MSA studies, and customer-specific requirements.
Yes. The FDA's Quality Management System Regulation became effective February 2, 2026. It incorporates ISO 13485:2016 by reference and gives the FDA explicit authority to inspect supplier audit reports, internal quality audits, and management review records.
ExceleorQMS is our digital quality platform that provides supplier scorecards, audit automation, CAPA tracking, and document control. It integrates with every consulting engagement to sustain gains and provide ongoing visibility into supplier performance.
Yes. We offer quarterly supplier risk monitoring retainers that include ongoing performance tracking, re-assessment of risk scores, and proactive escalation when supplier health indicators deteriorate.
Schedule a free consultation with our certified Lead Auditors. We'll diagnose your top supplier quality gaps and give you a clear path forward.