ISO/IEC 17025:2017 LEAD ASSESSOR (CQI IRCA) TRAINING

LIVE VIRTUAL TRAINING SCHEDULE

• 12th - 16th October 2020: ISO/IEC 17025:2017 Lead Assessor Training
  Day 1 - 4: 9 am to 6 pm (Virtual Training) | Day 5: 9 am - 1 pm (Classroom Training) & 2 - 5 pm (Exam)

• 7th - 11th December 2020: ISO/IEC 17025:2017 Lead Assessor Training
  Day 1 - 4: 9 am to 6 pm (Virtual Training) | Day 5: 9 am - 1 pm (Classroom Training) & 2 - 5 pm (Exam)

ABOUT THE COURSE

The purpose of this training course is to provide knowledge and skills required to perform first, second and third-party assessments of laboratory QMS against ISO/IEC 17025, in accordance with ISO 19011 and ISO/IEC 17011, as applicable. This training course has been adapted to requirements of ISO/IEC 17025 for the competence in testing and calibration laboratories.

Capitalizing on the powerful Accelerated Learning Technique, this course spends a good portion of the time on discussions, exercises and case studies to help students to consolidate knowledge and acquire hands on experience that are instrumental in their capacity as a QMS auditor or as a quality professional in a laboratory environment. Students who passed the continuous assessment and the 2-hour closed book examination will be awarded a Certificate of Achievement. This course satisfies the training requirement for certification as a CQI IRCA registered QMS Lead Auditor/Auditor.

Duration: 5 - day course

WHAT WILL YOU LEARN FROM THE COURSE?

On completion, successful students will be able to:

Knowledge

• Describe the purpose of a QMS and the technical requirements of ISO/IEC 17025
• Explain the role of an assessor to plan, conduct, report and follow up an assessment in accordance with ISO/IEC 17011

Skills

• Plan, conduct, report and follow up an assessment of a laboratory based on ISO/IEC 17025

Topics to be covered in this course include:

• General introduction
• ISO 9000 series and laboratory QMS; ISO/IEC 17025 requirements
• Document and record review
• Assessment planning
• On-site assessment; Assessment skills
• Reporting NC reports
• Assessment report and follow up

WHAT IS THE COURSE METHODOLOGY?

There is a balance between knowledge-based presentation, discussions, exercises and case studies. About two third of the time is spent on activity based learning. A mock examination paper will be discussed throughout the course to help students to be familiar with the style of the examination. Certificates will only be issued to participants with 100% full attendance.

WHO SHOULD TAKE THE COURSE?

This course is specially designed for:

• Staff who are responsible to establish, implement and maintain a laboratory QMS
• Potential assessors nominated by accreditation bodies who wish to receive an intensive training in order to fulfill the prerequisite requirements of assessors/lead assessors
• Those who wish to explore career opportunities in testing and calibration laboratories

Prerequisite:

CQI IRCA recommends that students are expected to have the following prior knowledge:

• QMP and concepts: the Plan, Do, Check, Act (PDCA) cycle; the relationship between QM and customer satisfaction; QM terms and definitions and the 8 Q Principles as given in ISO 9000; the process approach used in QM; The QMS Process Model, the structure and content of ISO 9001.
• The requirements of ISO 9001 and ISO/IEC 17025, which may be gained by completing a CQI IRCA certified QMS Foundation Training course or equivalent.

WHO IS THE COURSE ADVISOR?

The course content and structure are designed by the domain experts from TÜV SÜD.

With immense experience and knowledge in the relevant standards, our team of product specialists and technical experts at TÜV SÜD, developed the course content based on current business landscape and market requirements.