The training for Lead Auditor Course of ISO 9001:2015 can help an individual to understand, implement and evaluate the importance of each and every substance of a management system.

TQCAS will provide International Register of Certificated Auditors (IRCA) approved training from one of its business partners for promising Quality Management Systems Lead Auditors based on ISO 9001:2015. ISO 9001:2015 Lead Auditor course will be a 5 day course. This course will provide delegates with an in-depth knowledge as emphasis will be given to practical application of assessment skills.

Topics covered in the 5 day Training:

  • Introduction to Quality and ISO 19011
  • Types of Audits
  • Understanding the ISO 9001:2015 Standard requirements
  • Pre-audit management
  • Desktop Audit/Quality Manual Review
  • Audit Programming
  • Conducting an Opening Meeting
  • Audit Methods and Techniques
  • Syndicate Presentations
  • Audit Design Activities
  • Quality Audit Process
  • Raising Non-Conformances
  • Conducting a Closing Meeting
  • Writing the Audit Report
  • Audit Follow up Actions
  • Clearance of Non-Conformance Reports
  • Lead Auditor’s Management Responsibilities
  • Auditor Code of Conduct
  • IRCA Auditor Registration Scheme

Benefits of QMS Lead Auditor Training:

  • All the people who have successfully finished the training course will be able to apply ISO 9001:2015 standard in any organization or industry.
  • The person involved in the training will get ability to effectively use their interviewing skills and thus will help the organization to keep the right person for a particular process.
  • Reports which will be generated by trained person will be accurate and clear post completion of the course.
  • Trained people will exhibit knowledge and required skills to initiate and lead a management systems audit.
  • The person will be able to gauge if all the objectives evidences involved in the process are in agreement with ISO 9001:2015
  • With the help of this course, person will be able to effectively find and document the non-conformities which will enable him to take the required corrective actions.

Who should attend the training?

  • Management Representatives
  • Quality Directors
  • Managers
  • Engineers
  • Consultants