QMS Software for Manufacturing
End paper SOPs, spreadsheet trackers and missed corrective actions on the shop floor. With QualityWeb 360 your manufacturing QMS lives in the cloud — built for SOPs, CAPA, supplier evaluation and audits.
Discover the QMS software for manufacturers that drives continuous improvement on the shop floor
Why is your manufacturing QMS still living in Excel and shared drives?
If any of these problems sound familiar, it's time to discover QualityWeb 360.
Paper SOPs going stale
Your SOPs and work instructions live in printed binders that get outdated the day after they're printed.
Slow root-cause analysis
Non-conformances logged on paper — root-cause analysis comes days later, after memory fades.
Supplier blind spots
Supplier evaluations live in Excel files nobody trusts, leaving you exposed to upstream quality failures.
Key Modules for Manufacturing Quality
Four QualityWeb 360 modules built around the workflows that matter on the shop floor — from version-controlled SOPs to closing supplier non-conformities.
Document Control
Manage SOPs, work instructions and technical drawings with version tracking, approval workflows and automatic obsolescence.
See moduleModuleCorrective Actions
Log non-conformities from the line, run root-cause analysis (5 Whys, Ishikawa, 8D) and verify effectiveness — all timestamped for audits.
See moduleModuleSuppliers Evaluation
Qualify, score and re-evaluate suppliers. Track incoming non-conformities and protect your supply chain from upstream quality failures.
See moduleModuleInternal Audits
Plan, execute and document internal audits per ISO 9001, IATF 16949 or AS9100 requirements. Export evidence by clause.
See moduleFAQ
Manufacturing QMS — Frequently Asked Questions
Resolve the most common doubts in a single click.
QualityWeb 360 is built on the ISO 9001:2015 framework, which is the common foundation for IATF 16949 (automotive), AS9100 (aerospace) and ISO 13485 (medical devices). You can document the additional clauses, audits and traceability requirements using the same modules: document control, internal audits, CAPA, suppliers evaluation and records.
Yes — the Document Control module handles SOPs, work instructions, technical drawings, calibration procedures and any controlled document. Every version is tracked, every approval is logged with timestamps, and obsolete versions are automatically retired from active use.
Operators or QA staff can log non-conformities directly from any device (web or mobile) — describing the defect, attaching photos, tagging the affected lot or product. The case enters the CAPA workflow with assignable responsibles and deadlines, all timestamped for audit trail.
Yes — the Corrective Actions module supports 5 Whys, Ishikawa (fishbone) diagrams and 8D problem solving. You can document each step, link evidence, define corrective and preventive actions, and verify effectiveness — all timestamped for audit traceability.
Yes — the Suppliers Evaluation module supports initial qualification, periodic re-evaluation with custom criteria (delivery, quality, price), and supplier scoring. Incoming non-conformities are linked directly to the supplier, building an audit trail of performance over time.
Most manufacturing SMEs are fully operational in 2-4 weeks: one week to migrate existing documentation, one week to configure non-conformance and CAPA workflows, and 1-2 weeks of staff training. Larger plants with multiple lines may take 4-8 weeks.
Yes — onboarding includes role-based training: QA managers get advanced setup, shop-floor operators get a lightweight introduction focused on logging non-conformities and accessing current SOPs. Our 24/7 support center has tutorials in plain language, not just for technical users.
Yes — every action in QualityWeb 360 generates an audit trail (who, what, when). For ISO 9001, IATF 16949 or AS9100 external audits, you can export evidence reports filtered by clause directly from the platform, saving days of pre-audit preparation.
You have our 60-day "Love it or leave it" guarantee — full refund, no questions asked, if the platform doesn't fit your operation. You also keep download access to all your documents and data at any time, even after cancellation.
All data is hosted on AWS servers certified ISO 27001. Continuous backups guarantee instant service restoration in case of interruption. Role-based access means operators see only what they need, while QA and plant managers get full visibility. Data residency options available for regulated sectors.
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