ISSO/IEC17025: 2017 Lead Auditor Quality Management System
CQI & IRCA COURSE
Course Overview
- DELIVERY LANGUAGE: English and French
- FEATURES & BENEFITS: Gain first class auditing skills and start your journey in becoming a certified 3rd party auditor for ISO 50001:2018 Standard.
- COURSE CERTIFICATION: This course is fully recognized by CQI & IRCA
- DELIVERY METHOD: 70% Instructor Led 30% Role Plays & Case Studies
- COURSE PRE-REQUISITE: Learners are required to be familiar with ISO/IEC
17025:2017 requirements or have completed a recognized QMS Fundamentals course based on ISO/17025:2017 prior to registering for this course.
- COURSE OVERVIEW: Develop the skills to professionally audit a quality management system, and objectively assess compliance
Programme Details
of laboratories to meet accreditation body requirements, with our CQI and IRCA certified ISO/IEC 17025 Lead Auditor training course
Delegates on this in-depth course will learn how to conduct internal and external quality management systems audits against ISO/IEC 17025. They will develop the knowledge and skills to:
- Plan, conduct, report and follow up internal and external audits against ISO 17025, in line with ISO 19011 and ISO 17021 as applicable
- Promote the role of audits within the organization’s overall management system program, and the role of auditors in supporting laboratory compliance and competency improvements
- This practical, intensive and highly interactive 5-day course is based around a central case study and workshops, enabling students to practice their newly acquired skills.
- Delegates will achieve the formal training requirements to allow progression to becoming a CQI and IRCA Registered QMS Lead Auditor. Students are assessed by continuous evaluation and written exam.
LEARNING TOPICS:
- Quality and its assurance
>Introduction to auditing
>ISO 17025 and other ISO standards
>Documented systems
>Audit planning
>Checklist
>Opening meetings
>Nonconformity writing
>Auditing techniques
>Closing meetings
>Audit reporting
>Closing meeting
>Follow up and corrective action
1st, 2nd and 3rd party audits
HOW WILL I BE ASSESSED?
The delegate is assessed based on participation and performance throughout the duration of the course. This includes all exercise, role plays, case studies and all other activities during the course. Please note, full attendance is required during the training course.
There is a 2-hour written examination at the end of the course. The exam is closed book in that a delegate is entitled to use only their copy of the International Standards in question or dictionary if delivery language is not their native language. The minimum pass rate for the examination is 70%.
WHO SHOULD ATTEND?
This course is suitable for individuals in organization’s interested in operating effective laboratory management systems. They include:
- Those seeking to undertake 1st, 2nd and 3rd party audit against ISO 17025
>Laboratory quality and technical managers, technicians and Supervisors
>Supplier quality auditors wishing to evaluate laboratory services suppliers
>Existing auditors who wish to expand their skillset
NEBOSH Diploma Tutor | North Africa’s 1st Chartered IOSH Member & CSP | Co-Founder & CEO at Safeness | +23 years experience
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