ISO Training • Internal Auditor Certification • Lead Auditor Certification (ISO 9001, ISO 13485, AS9100, IATF 16949)
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Z L G (Zerimar Lagnar Group) provides Quality Management System (QMS) training, including awareness/implementation workshops, Internal Auditor certification, Lead Auditor certification, gap assessments, and audit preparation support.
We provide training and auditor certification for ISO 9001, ISO 13485, AS9100, and IATF 16949.
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.
Our training is designed for:
Yes. We offer live virtual, on-site, and hybrid formats. Content can be customized for single-site or multi-site organizations.
Yes. We tailor training using your procedures, forms, risks, and audit history to make the content immediately usable.
Yes. Z L G provides audit mentoring, gap assesments, pre-certification readiness reviews, and ongoing advisory support.
Core content includes standard overview, ISO 19011 principles, audit planning and checklists, interviewing, evidence collection, nonconformity writing, reporting, and corrective action verification.
Typically 1–2 days depending on the standard, audience experience, and customization level.
Yes. Certification requires course attendance, a written exam, and participation in audit exercises.
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.
Recommended prerequisites include Internal Auditor training and a working knowledge of the applicable standard. Prior quality/compliance experience is strongly recommended.
Typically 3–5 days depending on the standard and training format.
Participants learn clause intent, process auditing, risk-based thinking, and how to identify and document objective evidence and nonconformities that stand up to certification audit scrutiny.
Yes. We cover validation (IQ/OQ/PQ) auditing expectations, CAPA effectiveness, record integrity, and audit trails commonly reviewed in regulated environments.
Yes. We cover product safety planning and responsibilities, counterfeit parts controls, and configuration management/change control evidence expectations.
Yes. We cover how to audit APQP, PPAP, FMEA, MSA, and SPC, plus customer-specific requirements readiness.
Tell us your industry, sites, headcount, and target certification timeline—we’ll recommend the right course and format.