01

QMS Gap Analysis & Implementation

ISO 9001:2015 AS9100 Rev D IATF 16949
Whether you're preparing for initial certification, a surveillance audit, or you know your QMS has gaps — this service delivers a clear, evidenced picture of where you stand and a structured plan to get you to compliance.

Starting with a clause-by-clause gap analysis against your chosen standard, the engagement produces a documented findings report with graded conformance status and a prioritised remediation roadmap. Implementation support is available at whatever depth required — from advisory guidance through to full document development and pre-certification readiness review.

Deliverables

  • Written gap analysis report — clause-by-clause conformance status
  • Prioritised remediation plan with effort estimates
  • QMS documentation developed to standard requirements
  • Process interaction map and quality objectives register
  • Pre-certification readiness review and internal audit
  • Management review facilitation and minutes
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02

Internal & Supplier Auditing

ISO 19011 ISO 9001:2015 AS9100 Rev D
Internal and supplier audits are only valuable if they produce findings that reflect reality. This service provides rigorous, evidence-based auditing that will hold up under scrutiny — from your certification body, a customer, or a regulatory authority.

Audits are conducted in accordance with ISO 19011 and can be structured as clause-by-clause, process-based, or supplier qualification assessments. All findings are formally graded (Major NC, Minor NC, Observation, OFI) with objective evidence recorded. A formal audit report is issued after every engagement.

Deliverables

  • Annual audit programme and individual audit plans
  • Clause-by-clause or process-based audit execution
  • Formal audit report with graded findings and objective evidence
  • Audit findings log and corrective action tracking matrix
  • Supplier qualification audit reports
  • Opening and closing meeting facilitation
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03

NCR & CAPA Management

ISO 9001 Cl.10 8D 5 Whys Ishikawa
Recurring nonconformances, unresolved CARs, or a CAPA process that doesn't reach verified root cause — these are common, and they compound. This service gets your NCR/CAPA process working as the standard intends.

Nonconformances are investigated using structured root cause analysis — 8D, 5 Whys, and Ishikawa as appropriate to the complexity and consequence of the issue. Corrective action plans are developed with clear ownership, timescales, and effectiveness verification criteria. Systemic issues are escalated to management review.

Deliverables

  • Nonconformance investigation and formal NCR documentation
  • Root cause analysis using 8D, 5 Whys, or Ishikawa
  • Corrective action plans with verifiable acceptance criteria
  • CAPA tracker and status register
  • Effectiveness review and formal closure
  • NCR trend analysis and management review input
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04

Quality Documentation

ISO 9001 Cl.7.5 All sectors
Generic documentation that doesn't reflect how you actually operate will fail under audit. Quality documentation needs to be purposeful, controlled, and genuinely used.

Documented information is developed to clause 7.5 requirements — appropriate scope, controlled, version-managed, and written to reflect actual processes. All documents are authored in Microsoft Word and Excel for immediate use and straightforward revision by your team.

Deliverables

  • Quality manual aligned to ISO 9001:2015 clause structure
  • Mandatory and recommended procedures
  • Work instructions and process documentation
  • Operational forms: NCR, CAR, audit finding, change request
  • Document and record control register
  • Documented information control procedure (Cl.7.5)
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05

Defence Supply Chain Quality

SC Cleared AS9100 Rev D AQAP 2110 AQAP 2310
Defence and aerospace quality requirements go significantly beyond ISO 9001. If you're supplying into a prime contractor's supply chain, working towards AS9100 certification, or responding to AQAP contractual quality requirements, this service is built for your environment.

Delivered by a practitioner with 12 years' British Army service as an Ammunition Technician and CT EOD Operator. SC clearance held to October 2031. Work can be conducted in sensitive environments and on classified programmes.

Deliverables

  • AS9100 Rev D gap analysis (clause-by-clause vs. ISO 9001 baseline)
  • Quality plan authored to AQAP 2110/2310 format
  • First Article Inspection (FAI) and FAIR documentation
  • Supplier quality audit against AS9100 Rev D requirements
  • Key characteristics identification and control log
  • Configuration management and product/process change notification (PCN) documentation

SC clearance held to October 2031 (UKSV, 1_33A64FP). Note this in your enquiry if your programme involves classified material or a security-controlled environment.

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06

Programme-Level Quality Management

Government IT PRINCE2 Complex programmes
Large delivery programmes often inherit a QMS designed for something else, or have no coherent quality function at all. Embedded programme-level quality management prevents issues compounding across workstreams and delivery phases.

Drawing on direct experience building and remediating programme-level QMS in a multi-million pound government IT delivery programme, this service covers the full quality function for complex engagements. PRINCE2 Practitioner certified.

Deliverables

  • Programme quality plan and internal audit schedule
  • QMS gap analysis and remediation roadmap
  • Quality KPIs and management information reporting pack
  • Workstream-level internal audit programme
  • Management review facilitation and board-ready quality reporting
  • QA Lead coaching and embedded quality function support
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07

Training & Coaching

ISO 9001 ISO 19011 QA Leadership
A quality system is only as strong as the people maintaining it. Whether you need internal auditors trained, a QA Lead developed, or your team's understanding of ISO 9001 brought up to standard, this service builds internal capability.

Training is practical, sector-relevant, and tailored to your team's existing knowledge level. It is not generic classroom content. Internal auditor training covers the full audit cycle with worked examples relevant to your industry. QA Lead coaching is delivered as a structured programme over an agreed period.

Deliverables

  • Internal auditor training (ISO 19011-aligned, full audit cycle)
  • ISO 9001:2015 awareness training for staff and management
  • QA Lead 1:1 coaching programme
  • Root cause analysis workshop (8D, 5 Whys, Ishikawa)
  • NCR/CAPA investigation training with practical exercises
  • Written training materials and reference guides
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08

QMS Document Review

ISO 9001:2015 All sectors
If you already have a QMS but want an independent expert review of your documented information before an audit or certification assessment — this service provides exactly that, without the commitment of a full implementation engagement.

Your existing quality manual, procedures, forms, and documented information are reviewed against ISO 9001:2015 (or your applicable standard). A written report identifies gaps, areas of non-compliance, and documents requiring revision — with specific, actionable recommendations.

Deliverables

  • Review of all submitted quality documents
  • Written report with clause-referenced findings
  • Prioritised list of required changes
  • Specific revision recommendations for each document
  • Optional follow-on support to implement recommended changes
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