ISO/IEC 17025:2017 Testing and Calibration laboratories
About Course:
The ISO/IEC 17025:2017 Lead Auditor course is a specialized training program designed for professionals in the testing and calibration laboratory industry. This course equips participants with advanced knowledge and skills to lead and manage audits based on the ISO/IEC 17025:2017 standard, which sets the requirements for competence and quality in testing and calibration laboratories. Participants will gain expertise in audit planning, risk assessment, compliance verification, and the application of ISO/IEC 17025 standards to enhance laboratory quality and competence.
Learning outcomes of this course:
Upon completion of the Certified in ISO/IEC 17025:2017 Lead Auditor course, participants can expect to achieve the following learning outcomes:
- Master the principles and intricacies of ISO/IEC 17025:2017 for testing and calibration laboratories.
- Lead all phases of the audit process, from planning to report.
- Apply advanced auditing techniques and methodologies specific to laboratory quality.
- Plan and conduct audits effectively, including risk assessment and objective setting.
- Evaluate the compliance of testing and calibration laboratories with ISO/IEC 17025 standards.
- Communicate audit findings persuasively and provide actionable recommendations.
- Lead continuous improvement initiatives in laboratory quality and competence.
What will you learn?
The course content of the Certified in ISO/IEC 17025:2017 Lead Auditor course typically covers a range of advanced topics. Here are the topics covered:
- Introduction to ISO/IEC 17025:2017 and Laboratory Quality Auditing
- Role and Responsibilities of a Lead Auditor in Laboratory Quality Audits
- Understanding Quality Management Principles and ISO/IEC 17025:2017 Requirements
- Planning and Preparation for Laboratory Quality Audits
- Conducting Effective On-Site Audits: Techniques and Strategies
- Risk-Based Audit Planning and Objective Setting
- Documenting Audit Findings and Observations in the Context of Laboratories
- Non-Conformity Identification and Root Cause Analysis
- Developing Corrective and Preventive Action Plans for Laboratory Quality
- Reporting Audit Results and Recommending Improvements in Laboratory Quality
- Managing Auditor Teams and Audit Program for Laboratories
- Leading Continuous Enhancement in Laboratory Quality Audits
Evaluation Criteria:
The evaluation criteria for the Certified in ISO/IEC 17025:2017 Lead Auditor course may involve the following criteria:
- Written exams and assignments to evaluate understanding of ISO/IEC 17025:2017.
- Active participation in discussions, case studies, and practical exercises.
- Successful completion of lead auditor role-plays scenarios.
- Performance in written examinations or assessments covering course content.
Entry Criteria:
Participants should possess a strong understanding of laboratory quality management principles, auditing practices, and relevant standards. Prior experience in laboratory management, testing, calibration, or auditing is recommended.
Duration of Study:
Recommended Study Duration: 7 days