
- ISO Standards
- 40 hours
Objectives
This CQI & IRCA training course provides participants with in-depth Quality Assurance knowledge and Auditing Know-how.
- Highlight the significant changes on the new 2015 standard as compared to the interpretation and application of the current Standard.
- Focus on the appreciation of The Seven Quality Management Principles, ISO 9001, ISO 19011 and ISO/IEC 17021 Standard requirements.
- Strengthen the foundation of audit methodology, skill & techniques to perform audits and draw audit conclusion based on audit findings.
- Learn how to lead an audit team, conduct opening & closing meetings, collection of audit evidence against audit criteria and to present audit findings.
Duration
5 days | 9am – 5pm | 40 hours
Who should attend
Executives, Supervisor, Engineer, Managers, Safety Officer, Quality Professionals and Management Consultants who wishes to acquire this qualification as one of the pre-requisite for registration of CQI & IRCA QMS Auditor/Lead Auditor OR to enhance their professional auditing skills.
Entry Requirement
With reference to the latest CQI & IRCA requirements, you are expected to acquire the following prior knowledge before attending the class:
- The Application of Plan, Do, Check, ACT (PDCA) Cycle in all processes within a Quality Management System.
- The Seven Quality Management Principles and Its Application in The Context of ISO 9001:2015.
- Commonly used Quality Management Terms and Definitions in Relation To ISO 9001:2015.
- The adoption of “Process Approach” and “Risk-based Thinking” in formulating Quality Management System requirements.
- The Model of a Process Based Quality Management System, showing the links to the clauses of this standard.
Special Note
CQI& IRCA reminds all certified QMS auditors that they must fulfil the transition requirements for the ISO 9001:2015 update before completing any audits against the new standard.
Course Fees
Member Fee: S$1,995.35
Non-Member Fee: S$2,190.90
All fees stated are inclusive of Registration Fee, Exam & Certification Fees & 9% GST
Award of Certificate
Certificate of Achievement (CQI & IRCA certified)
Course Content
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Understanding the requirements of ISO 9001:2015, ISO 19011:2011 and ISO/IEC 17021:2011 Standards
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Changes arising as a result of the adoption of Annex SL (The Management System Writer’s Standard)
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Major differences In Terminology Between ISO 9001:2008 & ISO 9001:2015
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Application of the “Seven Quality Management Principles”, “Plan, Do, Check, Act (PDCA) Cycle” & “Process Approach”
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Risk-based Thinking in Formulating Quality Management Systems Requirements
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Terms & Definition: Audit, Audit Objective, Audit Scope, Audit Criteria, Audit Evidence, Audit Findings & Audit Conclusion
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Six Principles of Auditing and Their Application (Ref: ISO 19011:2011)
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Audit Plan vs Audit Program / Management of an Audit Program (Ref: ISO 19011:2011)
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Six Essential Steps in Performing an Audit (Ref: ISO 19011:2011)
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Responsibilities and Authorities of Auditor and Lead Auditor
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Prepare Audit Plan, Audit Checklist and Corrective Action Form
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Execution of Audit by Applying the Six Points of Audit Methodology (Ref: ISO 19011:2011)
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Documenting Non-conformity / Non-compliance, Corrective Action & Follow up Verification Audit
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Analysis and Presentation of Audit Findings and Audit Conclusion
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How to deal with classic problems during an audit?
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Desk-top audit session (Case study with role play)
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