ISO 17025 Lead Auditor: Ensuring trustworthy results in testing and calibration laboratories
ISO 17025 Lead Auditor Certification shows a person’s capabilities in reviewing laboratory management systems in accordance with ISO 17025. Recognized worldwide, the certification lays the foundation for minimum requirements regarding impartiality, high quality, and technical competence within testing and calibration laboratories. ISO 17025 Lead Auditor Certification demonstrates competence of standard along with knowledge of in-depth theories. The professionals who acquire this certification, acquire the knowledge and skills which access the knowledge of audit extensively and assess the compliance of the laboratory documentation. Furthermore, these professionals are able to see gaps in the system of operation and ways of improving them. The certification enables them to conduct tests that are consistent, authentic, and acceptable which builds trust and boosts goodwill and confidence in the market and in the prevailing industry.
What is the role of a lead auditor in managing ISO 17025 audit?
The management initiated by the lead auditor is of key importance who is responsible for audit conduction. The Lead Auditors supervise an audit team defining rational use of resources and fulfilment of the timetable by adhering to ISO 17025 standard. They function as the main link between the lab, being the one who holds the opening and closing meetings nurturing the communication in the process. During the audit, the Lead Auditor pays serious attention to the audit results and makes sure they are exact and full. Ultimately they bring all these results to a conclusion and compose an audit report to show the evaluation result of whether or not the laboratory adheres to ISO 17025:2017 standard.
Fastrack your career: Earn your ISO 17025 Lead Auditor Certification in Laos
ISO 17025 Lead Auditor Training in Laos is for those who intend to lead laboratory accreditation audits with detailed information for audits. Candidates will get a thorough understanding of the requirements for quality management systems, technical competence, and testing and calibration processes. The program covers detailed audit techniques inclusive of strategic planning, interviewing skills, and precise documentation of evidence. After completing the course of training, participants are required to sit for a rigorous examination to demonstrate their auditing knowledge. This evaluation consists of 20 multiple-choice questions and it is necessary to score 70% within 2 hours in order to be granted the Lead Auditor qualification.
Corporate Group Training
- Customized Training
- Live Instructor-led
- Onsite / Online
- Flexible Dates
ISO 17025 Lead Auditor Exam Format | |
Exam Name | ISO 17025 Lead Auditor Certification |
Exam Format | Multiple choice, subjective |
Total Questions | 20 Questions |
Passing Score | 70% |
Exam Duration | 2 Hours |
Key Features of ISO 17025 Lead Auditor Certification Training in Laos
ISO 17025 Lead Auditor Training program in Laos by Unichrone, offers a comprehensive curriculum designed to lead professionals towards successful laboratory accreditation audits. The program provides a thorough exploration and knowledge of the ISO 17025 standard. This ensures a deep understanding of its critical requirements for laboratory quality management systems. The training program includes technical competence needs, testing and calibration processes, and the overarching principles of laboratory management. During the training, professionals will gain proficiency in advanced audit methodologies. Through practical exercises, mastering the art of effective audit planning, insightful interview techniques, and meticulous documentation they will be equipped with a complete audit picture. The training program will equip professionals with comprehensive exam preparation with insightful resources. Upon successful completion, professionals will earn a globally recognized ISO 17025 Lead Auditor certification.
- 4 Day Interactive Instructor –led Online Classroom or Group Training in Laos
- Course study materials designed by subject matter experts
- Mock Tests to prepare in a best way
- Highly qualified, expert & accredited trainers with vast experience
- Enrich with Industry best practices and case studies and present trends
- ISO 17025 Lead Auditor Training Course adhered with International Standards
- End-to-end support via phone, mail, and chat
- Convenient Weekday/Weekend ISO 17025 Lead Auditor Training Course schedule in Laos
ISO 17025 Lead Auditor Certification Benefits
Higher Salary
With this renowned credential, aspirants earn higher salary packages when compared to non-certified professionals in the field
Individual accomplishments
Aspirants can look for higher career prospects at an early stage in their life with the most esteemed certification
Gain credibility
Owning the certification makes it easier to earn the trust and respect of professionals working in the same field
Rigorous study plan
The course content is prescribed as per the exam requirements, covering the necessary topics to ace the exam in the first attempt
Diverse job roles
Attaining the certification enhances the spirit of individuals to pursue diverse job roles in the organization
Sophisticated skillset
With this certification, individuals acquire refined skills and techniques required to play their part in an organization
ISO 17025 Lead Auditor Course Curriculum
-
Module 1: Introduction to ISO 17025
Topics
- · ISO 17025
-
Module 2: Requirements of ISO 17025
Topics
- · Overview
-
Module 3: ISO 19011 Relationship to ISO 17025
Topics
- · ISO 19011
- · ISO 17025
-
Module 4: Scope
Topics
- · Overview
-
Module 5: Normative References
Topics
- · Introduction to Normative References
-
Module 6: Terms and Definitions
Topics
- · Overview
-
Module 7: General Requirements
Topics
- · Overview
- · Impartiality
- · Confidentiality
-
Module 8: Structural Requirements
Topics
- · Overview of Structural Requirements
-
Module 9: Resource Requirements
Topics
- · Introduction
- · General
- · Personnel
- · Facilities and Environmental Conditions
- · Equipment
- · Metrological Traceability
- · Externally Provided Products and Services
-
Module 10: Process Requirements
Topics
- · Introduction to Process Requirements
- · Review - Requests, Tenders, and Contracts
- · Selection, Verification, and Validation of Methods
- · Sampling
- · Handling Test or Calibration Items
- · Technical Records
- · Evaluation of Measurement Uncertainty
- · Ensure Results Validity
- · Reporting of Results
- · Complaints
- · Nonconforming Work
- · Control of Data and Information Management
-
Module 11: Management System Requirements
Topics
- · Options
- · Option A
- · Option B
- · General
-
Module 12: Management System Documentation
Topics
- · Overview
- · Document Categories
-
Module 13: Control Management System Documents
Topics
- · Overview
- · Primary Document Control Requirements in the ISO 17025 Standard
-
Module 14: Control of Records
Topics
- · Overview
-
Module 15: Address Risks and Opportunities
Topics
- · Overview of Address Risks and Opportunities
-
Module 16: Improvement
Topics
- · Overview of Improvement
-
Module 17: Corrective Actions
Topics
- · Steps to Take Corrective Actions
-
Module 18: Management Reviews
Topics
- · Management Reviews
-
Module 19: Terminology – ISO 9000, VIM etc.
Topics
- · ISO 9000 Terminology in English
- · What is ISO 9000?
- · Common ISO Definitions
-
Module 20: Fundamental Audit Concepts and Principles
Topics
- · Overview
-
Module 21: Auditing Requirements and Assessment: ISO 17011:2017, ISO 19011:2018
Topics
- · Auditing: ISO 17011:2017
- · Auditing: ISO 19011:2018
-
Module 22: Recognition and Oversight of ILAC, IAAC, APAC etc.
Topics
- · Description of ILAC
- · ILAC’s Global Role
- · Abbreviations
- · ILAC Documents
- · ILAC P10 Traceability Policy
-
Module 23: Test Reports, AB Symbols, Equipment Stickers, and Certificates
Topics
- · AB Symbols
- · Certificates
- · Certificate Naming Convention
-
Module 24: Clauses 4, 5, and 6 Review
Topics
- · Case studies on clauses 4, 5 and 6
-
Module 25: Clauses 7 and 8 Review
Topics
- · Case studies on clauses 7 and 8
-
Module 26: Guidelines for Auditing: ISO 19011
Topics
- · ISO 19011 Auditing Guidelines
- · What is ISO 19011?
- · Standard Facts of ISO 19011
- · Who ISO 19011:2018 should be Used?
- · What does ISO 19011:2018 Accomplish?
-
Module 27: GUM (Uncertainty), PT/ILC, and Traceability
Topics
- · GUM (Uncertainty)
- · PT/ILC
- · Traceability
-
Module 28: Opening and Closing Meeting Activities
Topics
- · Opening Meeting
- · What Happens in an Opening Meeting?
- · Closing Meeting
- · What Happens in a Closing Meeting?
-
Module 29: Auditing Technical Methods
Topics
- · Auditing Technical Methods
-
Module 30: Reporting Audit Results
Topics
- · Reporting Audit Results
-
Module 31: Audit Checklists and Audit Reports
Topics
- · Audit Checklists and Audit Reports
-
Module 32: Review of Standards and Internal Auditing Issues
Topics
- · Review of Standards
- · Internal Auditing Issues
-
Module 33: Introduction to Lab Management System (LMS)
Topics
- · Standards and regulatory frameworks
- · Laboratory management systems
- · Laboratories and accreditation fundamental principles
- · Testing and calibration concepts
- · Implementation of LMS
- · Understanding the organisation
- · Analysing existing systems
-
Module 34: Planning LMS Implementation
Topics
- · Leadership and LMS project approval
- · Scope of LMS
- · Laboratory policies
- · Organisational structure
- · Document management process
-
Module 35: Implementing an LMS
Topics
- · Design of controls
- · Drafting of specific policies and procedures
- · Communication planning
- · Training and awareness planning
- · Resource management
- · Customer management
- · Operations management
-
Module 36: LMS Monitoring, Measurement, and Continuous Improvement
Topics
- · Monitoring, analysis, and evaluation
- · Treating problems and nonconformities
- · Continual improvement
- · Accreditation preparation
- · Implementers evaluation
-
Module 37: Planning an ISO 17025 Audit
Topics
- · Audit approach
- · Preparing the ISO 17025 Audit
- · Conducting an opening meeting
-
Module 38: Conducting the ISO 17025 Audit
Topics
- · Communication during audit
- · Audit procedures
- · Observation
- · Document review
- · Interview
- · Sampling techniques
- · Technical verification
- · Corroboration and evaluation
- · Audit test plans
- · Formulation of audit findings
- · Documenting nonconformities
-
Module 39: Concluding and Follow-Up of ISO 17025 Audits
Topics
- · Audit documentation
- · Quality review
- · Closing meeting
- · Evaluation of corrective action plans
- · ISO 17025 surveillance audits
- · ISO 17025 internal audit management program
Frequently Asked Questions
For whom is ISO 17025 Lead Auditor Training in Laos generally meant for?
The ISO 17025 Lead Auditor Training in Laos is designed for professionals seeking to lead laboratory accreditation audits, ensuring laboratories comply with quality management systems and testing or calibration processes.
What are the prerequisites for enrolling in the ISO 17025 Lead Auditor Training in Laos?
The ISO 17025 Lead Auditor Training in Laos requires a general understanding of the quality management system and the ISO 17025 standard principles.
What topics are covered in the training course?
The topics which will be covered in the training are:
- Introduction to ISO 17025
- Requirements to ISO 17025
- The relationship between ISO 19001 and IS 17025
- Auditing technical methods
- Planning and implementation of audits
What is the format of the ISO 17025 Lead Auditor Training?
The format of the ISO 17025 Lead Auditor Training is both online and live instructor-led lectures.
What is the duration of the training program?
The duration of the training will be 4 days
What are the study materials included in the training program?
Study materials for the ISO 17025 Lead Auditor Training program typically include:
- Course manuals
- Presentations
- Practice exams and resources
Is there any pre-reading or preparation recommended before starting this course?
Pre-reading materials or familiarizing yourself with the ISO 17025 standard's basics can enhance your understanding during the ISO 17025 Lead Auditor Training program.
What format is the ISO 17025 Lead Auditor Certification Exam?
The format of ISO 17025 Lead Auditor Certification Exam is multiple-choice questions.
After completing the training is it necessary to sit for ISO 17025 Lead Auditor Exam?
To earn the ISO 17025 Lead Auditor Certification, it is necessary to pass the exam after completing the training.
What will be the duration of the ISO 17025 Lead Auditor Exam?
The candidates will be allotted 2 hours to complete the Lead Auditor exam.
What is the passing percentage for the exam?
To pass the Lead Auditor exam candidates need to score above 70%.
How many questions would be there in the exam?
In the exam, there will be a total of 20 questions in the format of multiple-choice and subjective which are required to be answered.
How is the ISO 17025 Lead Auditor Exam conducted?
The exam is offered online for those taking up live online instructor-led method and offline for those taking up in-classroom method of training.
What career opportunities are available for certified ISO 17025 Lead Auditors in Laos?
ISO 17025 Lead Auditors can find opportunities in laboratory accreditation bodies, consultancies, or within companies seeking to improve their own quality management systems.
Is the ISO 17025 Lead Auditor Certification recognized Internationally?
Yes, the ISO 17025 Lead Auditor Certification is recognized Internationally.
What are the ongoing maintenance requirements to retain the certification?
Retaining ISO 17025 Lead Auditor certification typically involves ongoing professional development activities and potentially re-certification exams to ensure continued competence in the field.
How long does it typically take to complete the training and become certified?
After completing the training, candidates are required to sit for an exam. After scoring the passing percentage of 70%, candidates will become certified Lead Auditors.
Can I acquire the ISO 17025 Lead Auditor Certification without sitting for an exam?
No, to acquire the ISO 17025 Lead Auditor certification sitting for an exam is necessary.
Will ISO 17025 Lead Auditor Certification offered by Unichrone help me in building my network?
While Unichrone's curriculum can't directly build your network, the knowledge and certification gained can open doors to industry events or professional organizations where you can connect with other ISO 17025 Lead Auditors.
What are the career benefits of earning a Lead Auditor Certification?
Lead Auditor Certification has various career benefits, including:
- Increased earning potential
- Enhanced credibility
- Career advancement
- Global recognition
- Increased job security
ISO 17025 Lead Auditor Examination Procedure
PREPARE
Go through the intense 4-day ISO 17025 Lead Auditor Training offered by Unichrone. Fulfil all the requirements before the examination.
APPLY
Apply for the ISO 17025 Lead Auditor Exam conducted by Unichrone. Choose the suitable date for the exam.
ACQUIRE
Get certified with ISO 17025 Lead Auditor after clearing the exam. You will receive an email confirming the status.
What our customers say
Register for a free session with our trainer
Select your city to view ISO 17025 Lead Auditor Certification Training Course Schedule in Laos
Faculty and Mentors
Our certified and highly experienced trainers are handpicked from various industries to assist aspirants with practical insights into the field, thereby providing a comprehensive understanding of fundamentals and complex terminologies
1200+
Instructors
20+
Minimum Experience
100+
Session Expertise
- Improved problem-solving skills
- Enhanced communication skills
- Staying current in the field
- Personal satisfaction
- Broaden skill set
- Testing laboratories
- Calibration laboratories
- Medical Laboratories
- Forensic laboratories and many more
- Enhanced red bitty and reputation
- Improved efficiency and cost savings
- Global recognition
- Stronger client relationships
- Competitive advancement
- Management system
- Technical competence
- Calibration and traceability
- Testing and calibration processes
- Data integrity
- Handling complaints
- Increased reputation and client confidence
- Improved efficiency and effectiveness
- Reduced costs
- Greater access to markets
- Personnel qualifications
- Training and skill development
- Technical records
- Technical procedure
- Equipment maintenance
Base
Understand the fundamentals
Accede
Recognize your talent
Acquiesce
Be awarded
Admit