LEAD AUDITOR COURSE

Types of ISO Lead Auditor Courses Offered by IAS

IAS delivers CQI-IRCA accreditedISO Lead Auditor Course in Malaysia for the following schemes:

We conducts the lead auditor course with real-time trainers as faculties. Our experienced trainers guide you through the entire audit process, from starting the review, to forming an audit report and initiating corrective actions to help companies achieve ISO certification.

Course Duration: 5 days, 40 hours

IRCA Examination: Participants will take the IRCA examination at the end of the ISO lead auditor course. Upon successful completion of the exam, candidates will receive an IRCA accredited ISO Lead Auditor CourseCompletion Certificate.

Who Can Apply for the ISO Lead Auditor Course?

  • Quality experts keen on leading first-party, second-party, or potentially third party audits
  • Management Representatives
  • Quality Representatives
  • Managers
  • Consultants
  • Food Safety Officers
  • EHS Managers and Executives

IRCA Accredited ISO Lead Auditor Training Course

Our ISO lead Auditor Courses are affirmed by the International Register of Certificated Auditors (IRCA) and meets the preparation prerequisites for IRCA Management Systems Auditor Certification criteria. Candidates who complete this ISO lead auditor course will become globally recognized IRCA Lead Auditors.

Benefits of ISO Lead Auditor Course in Malaysia

The aim of the ISO lead auditor course in Malaysia is to provide participants with the necessary skills and knowledge to plan, conduct and report an audit of an ISO management system. The benefits of attending this ISO lead auditor course in Malaysia include:

  • Understanding the principles and concepts of auditing
  • Developing the skills to plan and conduct an audit
  • Learning how to report on an audit
  • Understanding the requirements of ISO standards
  • Understanding the auditor’s role and responsibilities
  • Developing the ability to analyze management systems
  • Learning how to assess compliance with requirements
  • Developing problem-solving skills

Comments

Post a Comment

Popular posts from this blog

Iso 15189 Certification

Achieving ISO 15189 Certification assists medical laboratories in developing their quality management system and assessing their own competence. It can also be used for confirming or recognizing the competence of medical laboratories by regulating authorities, laboratory customers, and accreditation bodies. Overall, ISO 15189 certification demonstrates a laboratory’s commitment to providing accurate and reliable results. ISO 15189 in Malaysia is becoming increasingly popular as more medical laboratories are striving to become certified. IAS provides a very simple yet efficient ISO 15189 certification process to help your organization achieve ISO 15189 certification in a timely manner! Benefits of ISO 15189 Certification Implementing ISO 15189 in Malaysia can improve medical laboratory processes and increase customer satisfaction. With ISO 15189 certification, medical laboratories can: Enhance the quality of patient care by providing accurate results on tests Develop a systematic approa...
Read more

IATF 16949 CERTIFICATION

ABOUT IATF 16949 CERTIFICATION IATF 16949 certification establishes the requirements for a Quality Management System (QMS) specifically for automotive sectors. The ISO 16949 standard was initially formed in 1999 by International Automotive Task Force to coordinate different analysis and certification schemes globally in the supply chain for the automotive sector. The IATF 16949 standard provides guidance and tools for companies and organizations who want to ensure that their products consistently meet customer requirements and customer satisfaction is consistently improved. The main focus of the IATF 16949 standard is the development of a Quality Management System that assists in continual improvement, focus attention on defect prevention and the reduction of discrepancy and squander in the supply chain. The standard is consolidated with applicable Customer-Specific requirements that define the QMS requirements for automotive production, service, and/or accessory parts. IATF 16949 sta...
Read more

What are the 7 steps to HACCP?

  Hazard Analysis The first step in HACCP is hazard analysis. This step involves identifying all of the potential hazards that could occur during the production of a food product. hazards can be physical, chemical, or biological in nature, and can occur at any stage of the food production process. Critical Control Points The second step in HACCP is to identify the critical control points (CCPs). CCPs are those points in the food production process where a hazard can be controlled or prevented. There may be multiple CCPs for a single food product, and they will vary depending on the type of product being produced. Establishing Critical Limits The third step in HACCP is to establish critical limits for each CCP. A critical limit is a maximum or minimum value that must not be exceeded for a particular hazard. For example, a critical limit for bacterial growth might be an internal temperature of food that must not exceed 40 degrees Fahrenheit. Monitoring Procedures The fo...
Read more