Industries

Built to the strictest bar.
Applied across regulated industries.

SQOS runs the same supplier quality record, captured at the source, across regulated discrete manufacturing. The workflows and standards differ by industry; the system of record doesn't.

Aerospace & defense

Where first-article and full traceability are non-negotiable.

AS9100 AS9102 · FAI AS9145 · APQP/PPAP

First-article inspection, source inspection, and lot traceability aren't optional, and a customer or DCMA audit can pull any record at any time. Reconstructing it from email and spreadsheets is where programs lose time and lose trust.

How SQOS maps
  • FAI and AS9102 evidence captured against the part, not rebuilt after the fact.
  • Containment lives inside the SCAR, tied to the lot and disposition.
  • Export-controlled data handled with scoped, logged access, and CAC/PIV where required.

Automotive

High volume, tiered supply, zero tolerance for a line-down.

IATF 16949 PPAP · APQP 8D FMEA

PPAP submissions and 8D responses pile up across hundreds of suppliers, and a missed containment surfaces as a recall risk. The 8D discipline was born here; the tooling around it usually wasn't.

How SQOS maps
  • PPAP and APQP tracked to the part, program, and submission level.
  • 8D and SCAR run in-system, with containment tied to the lot.
  • Live supplier scorecards and chargebacks across the tier, not a monthly export.

Medical devices

Where the record has to stand up to an FDA inspection.

ISO 13485 21 CFR 820 · QMSR CAPA UDI

Device traceability and CAPA have to be complete and attributable, and a supplier nonconformance feeds directly into product risk. Gaps in the record are gaps in the audit.

How SQOS maps
  • Nonconformances and dispositions captured with full part and lot traceability.
  • Supplier corrective actions linked to the CAPA they belong to.
  • Every action logged, timestamped, and attributable for inspection.

Electronics & EMS

Fast NPI, many suppliers, workmanship standards that vary by customer.

IPC-A-610 J-STD ISO 9001

Inspection results and deviations need to move at the speed of the line, across a supplier base that turns over quickly and a set of acceptance criteria that changes by program.

How SQOS maps
  • Inspection routing and results captured at the source, as the work runs.
  • Deviations and dispositions tied to the part and lot.
  • Counts pulled from MES, so scorecards reflect what actually shipped.

Industrial & general manufacturing

Supplier quality that's real, but under-tooled.

ISO 9001

For a lot of manufacturers, supplier quality lives in a spreadsheet and a shared drive. It works until you try to scale it across sites and suppliers, and then the seams show.

How SQOS maps
  • One system of record across sites and suppliers.
  • SCAR/8D, NCR/MRB, and scorecards without the spreadsheet sprawl.
  • Connectors to the ERP and WMS you already run.

Energy

Long-lead, high-consequence components where an escape is expensive.

ISO 9001 Sector requirements

Components are long-lead and high-consequence, traceability is mandatory, and the quality record often has to outlive the people who created it and survive the life of the asset.

How SQOS maps
  • Full traceability from receipt through disposition.
  • Containment and corrective action tied to the part and lot.
  • Audit-ready records retained for the life of the asset.
See it in your world

Bring your standard. We'll map it.

Tell us your industry and the framework you answer to. We'll walk SQOS against the workflows and records that matter to you.