Training & Professional Certification
Build internal auditor and quality capability your certification depends on.
For: Teams that need qualified auditors and practical quality skills
- ISO 9001
- ISO 13485
- AS9100
- IATF 16949
New free resource: Certification Audit Readiness Checklist — no form required.
QMS Consulting Training & Certification English · Español
Practical ISO training, QMS implementation, internal auditing, certification support, quality applications, and professional staffing for regulated and manufacturing organizations.
The problems we solve
ZLG addresses these problems with practical training, independent audits, hands-on implementation, quality software, and staffing — built around how your organization actually works, and measured by operational results rather than certificates on the wall.
Services
Six services that work independently or together — from training a single auditor to running your entire quality system.
Build internal auditor and quality capability your certification depends on.
For: Teams that need qualified auditors and practical quality skills
Keep your quality system running — documents, audits, CAPA, KPIs — without adding headcount.
For: Organizations without a full-time quality team, or teams stretched thin
Independent, evidence-based internal audits that find issues before your certification body does.
For: Organizations needing impartial audits or a stronger audit program
Replace spreadsheets with connected quality software for documents, CAPA, inspections, and training.
For: Teams drowning in disconnected spreadsheets and shared drives
Go from gap assessment to certification-audit readiness with a system built for daily use.
For: Organizations pursuing initial certification or recovering from audit failures
Qualified quality professionals on your floor — for coverage, surges, or the long term.
For: Organizations with quality vacancies, surges, or special projects
How we work
Six steps from first assessment to a self-sustaining system. Expand any step to see who does what and what you receive.
Provide access to procedures, records, and key personnel for interviews.
Conduct the gap assessment and document findings with objective evidence.
Gap assessment report with prioritized findings.
A clear, evidence-based picture of where you stand.
Confirm business priorities, target dates, and resource availability.
Build the project plan with owners, milestones, and dependencies.
Project plan and responsibility matrix.
A realistic roadmap your team can commit to.
Review drafts and validate that documents match real practice.
Draft documentation, process maps, risk registers, and KPIs.
QMS documentation, process maps, KPI definitions.
A system built for daily use — not just for the audit.
Schedule participants and ensure attendance.
Deliver training with exercises built from your own procedures and findings.
Training records, competency evaluations, certificates.
A workforce that understands and runs the system.
Execute processes and raise issues as they surface.
Coach process owners, run internal audits, and support management review.
Internal audit reports, management review records, CAPA log.
Objective evidence that the system works in practice.
Own corrective actions and sustain the improvement cadence.
Verify effectiveness, refine metrics, and support ongoing audits.
Effectiveness verifications, updated KPIs, improvement log.
A quality system that keeps delivering after certification.
Industries
ISO 9001
Quality systems that reduce scrap, stabilize processes, and satisfy customer audits across general manufacturing.
Relevant servicesISO 13485
Regulated QMS support covering validation, CAPA effectiveness, record integrity, and audit trails.
Relevant servicesAS9100
Product safety planning, counterfeit parts controls, and configuration management evidence expectations.
Relevant servicesIATF 16949
Core Tools auditing — APQP, PPAP, FMEA, MSA, SPC — plus customer-specific requirements readiness.
Relevant servicesIPC / J-STD
IPC and J-STD workmanship training and inspection discipline for electronics assembly operations.
Relevant servicesAll standards
Consistent procedures, harmonized audits, and shared metrics across plants, in English and Español.
Relevant servicesWhat you can expect
Every engagement is aimed at operational results. These are the categories of improvement our clients pursue with us.
Walk into certification and customer audits with organized, objective evidence.
Corrective actions that reach root cause and stay closed.
An audit team that finds what matters before outsiders do.
Current documents, controlled changes, no obsolete copies on the floor.
Standard work followed the same way on every shift and every site.
Effectiveness verified on the job, not just attendance sheets.
KPIs leadership actually uses to run the business.
A CAPA system that prevents recurrence instead of producing paperwork.
Training & certification
Proof
Automotive · IATF 16949
Training plus live 8D coaching cut repeat customer complaints by more than half and cleared a year-old CAPA backlog.
Read case studyMedical Devices · ISO 13485
From zero documented QMS to certification recommendation in eleven months — without stopping a production ramp.
Read case studyAerospace · AS9100
How an independent internal audit program helped an aerospace supplier eliminate repeat findings and pass surveillance with zero majors.
Read case studyFree downloads
Checklist
A clause-by-clause internal audit checklist with space for objective evidence, aligned with ISO 19011 practice.
Get the resourceChecklist
The records, evidence, and logistics to have in place before your certification or surveillance audit.
Download freeTemplate
A structured 8D template with root cause analysis prompts and effectiveness verification built in.
Get the resourceWorksheet
Self-assess your quality system against ISO 9001 requirements and prioritize the gaps that matter.
Get the resourceWhat clients say
We had eleven months to reach ISO 13485 certification without slowing a production ramp. ZLG sequenced everything backwards from the audit date, and we passed Stage 2 with four weeks to spare.
After three surveillance audits with the same repeat findings, ZLG rebuilt our internal audit program in nine months. The next audit closed with zero majors — and our own team now runs the program with confidence.
Every exercise used our own procedures and our own findings. I planned and led a real audit two weeks after the course — that never happened with the generic training we tried before.
Credentials
Internal Auditor and Lead Auditor certifications follow ISO 19011 auditing guidance and industry best practices, with written exams and evaluated audit exercises.
Through our partnership with KCertification, clients can access accredited third-party certification for ISO 9001, ISO 13485, and ISO 14001 — independent of our consulting role.
Our consultants come from commercial, medical device, aerospace, automotive, and electronics manufacturing environments — and deliver in English and Español.
Certificate acceptance depends on your customer and certification body requirements. Certification decisions are always made by an independent certification body, never by ZLG.
About ZLG
Zerimar Legnar Group was built by quality professionals who have run production floors, closed real findings, and sat on both sides of the audit table. We teach what auditors look for, implement systems people actually use, and stay until the results are measurable.
Insights
QMS Implementation
The difference between audit-driven and operations-driven quality systems, and three signs your QMS is working for the certificate instead of the company.
Read articleCAPA & Problem Solving
Closed is not the same as effective. The discipline of effectiveness verification is what separates CAPA systems that work from CAPA systems that churn.
Read articleInternal Auditing
A weak nonconformity starts a debate. A strong one starts a corrective action. Here is the structure experienced auditors use.
Read articleQuestions
Our certifications are aligned with ISO 19011 auditing guidelines and industry best practices. The certificates are suitable for internal audits, supplier audits, second-party audits, and certification audit preparation. Acceptance depends on your customer and/or certification body requirements.
Internal Auditor training focuses on executing audits within your organization. Lead Auditor training prepares participants to plan, lead, manage, and report audits, including supplier and multi-site audits.
ZLG (Zerimar Legnar Group) provides Quality Management System (QMS) training — including awareness and implementation workshops, Internal Auditor certification, and Lead Auditor certification — plus QMS management, independent internal auditing, quality software applications, implementation and certification support, gap assessments, audit preparation, and professional quality staffing.
Yes. We offer live virtual, on-site, and hybrid formats. Content can be customized for single-site or multi-site organizations, and programs are available in English and Español.
We provide training, auditing, and auditor certification for ISO 9001, ISO 13485, AS9100, and IATF 16949, along with IPC and J-STD workmanship programs, Lean Manufacturing, and Six Sigma. Our auditing practice follows ISO 19011 guidance.
Tell us where you are — a deadline, a finding, a gap, a vacancy — and we will map the most direct path to a measurable result.
Prefer to talk? 712-430-4103 · info@zlgus.com
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