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ISO 9001 QMS Lead Auditor Course

ISO 9001 is an international standard for quality management systems (QMS), which helps organizations demonstrate their commitment to providing products and services of consistent quality. A Lead Auditor Course in ISO 9001 is designed to equip individuals with the knowledge and skills necessary to lead and conduct audits of quality management systems.

Course Name:

5 Days Quality Management Systems Lead Auditor Training Course based on ISO 9001

Learning Objectivea:

  • Understanding ISO 9001:

  • Gain a comprehensive understanding of the ISO 9001 standard, its structure, and its key requirements.

  • Quality Management Principles:

  • Familiarize yourself with the seven quality management principles that form the foundation of ISO 9001.

  • Interpreting Requirements:

  • Learn how to interpret and apply the specific requirements of ISO 9001:2015 to various organizational contexts.

  • Audit Planning and Preparation:

  • Develop skills in creating effective audit plans, including setting objectives, determining scope, and defining criteria.

  • Audit Techniques:

  • Acquire techniques for gathering and evaluating audit evidence, including interviewing, observation, and document review.

  • Conducting an Audit:

  • Learn how to conduct audits, including opening and closing meetings, and managing the audit process.

  • Audit Reporting:

  • Gain the ability to document audit findings, report nonconformities, and provide constructive feedback to auditees.

  • Corrective Action and Follow-Up:

  • Understand the process of identifying and verifying corrective actions, and ensuring their effectiveness.

  • Audit Team Management:

  • Develop skills in managing audit teams, including assigning roles, coordinating activities, and resolving conflicts.

  • Case Studies and Practical Exercises:

  • Apply theoretical knowledge through hands-on exercises, including role-playing and mock audits.

  • Certification Process:

  • Familiarize yourself with the certification process for lead auditors, including eligibility criteria and application procedures.

  • Continual Improvement and Best Practices:

  • Gain insights into strategies for ongoing improvement of quality management systems and share best practices.

  • Legal and Ethical Considerations:

  • Understand the legal and ethical responsibilities of auditors, including confidentiality and impartiality.

  • Final Assessment and Examination:

  • Demonstrate understanding and competence through a final exam or assessment.

Who should attend:

  • Quality Managers and Professionals: Those responsible for overseeing the quality management system within an organization.

  • Internal Auditors: Individuals who conduct internal audits of the organization's quality management system.

  • Lead Auditors: Individuals who lead and manage audit teams, and are responsible for planning and conducting audits.

  • Management Representatives: Individuals appointed by top management to ensure that the quality management system is established, implemented, and maintained.

  • Process Owners: Individuals responsible for specific processes within the organization, and who need to ensure compliance with ISO 9001 requirements.

  • Consultants: Quality management consultants who assist organizations in implementing and maintaining ISO 9001 compliance.

  • Professionals Seeking Career Advancement: Those looking to enhance their skills and knowledge in quality management, potentially for career progression.

  • Supplier Auditors: Professionals responsible for auditing suppliers to ensure compliance with ISO 9001 requirements.

  • Regulatory Compliance Officers: Individuals who need to ensure that the organization adheres to regulatory requirements, which may include ISO 9001 compliance.

  • Anyone Involved in Quality Management: This could include individuals from various departments within an organization who have responsibilities related to quality management.

Course Structure:

  • Introduction to ISO 9001

    • Overview and benefits.

  • Quality Management Principles

    • Seven key principles.

  • QMS Requirements (ISO 9001:2015)

    • Detailed study of standard clauses.

  • Audit Fundamentals

    • Basics of auditing.

  • Audit Planning and Preparation

    • Developing audit plans.

  • Audit Techniques

    • Gathering and evaluating evidence.

  • Conducting an Audit

    • Opening and closing meetings, on-site audits.

  • Audit Reporting

    • Preparing audit reports.

  • Corrective Action and Follow-Up

    • Implementing corrective actions.

  • Audit Team Management

    • Roles and responsibilities.

  • Case Studies and Exercises

    • Practical application.

  • Certification Process

    • Becoming a certified lead auditor.

  • Continual Improvement

    • Strategies for ongoing enhancement.

  • Legal and Ethical Considerations

    • Responsibilities of auditors.

  • Final Assessment and Examination

    • Evaluation of understanding and competence.

Contact Us:

For further information & schedule on ISO 9001 lead auditor training course, please contact us by email @ info@bcicertification.com or call us at +91 95604 72730. We will be happy to assist you.

FAQs

ISO 9001 and ISO 21001 are both international standards, but they focus on different aspects of organizational management. In summary, while both ISO 9001 and ISO 21001 are management system standards, ISO 9001 focuses on quality management in a broad organizational context, applicable to various industries. On the other hand, ISO 21001 is specifically designed for educational institutions and addresses the unique aspects of managing quality in an educational setting.

If you or your organization are currently certified to ISO 9001:2008, it's important to take action to transition to the latest version, which is ISO 9001:2015. Here are the steps you should consider:

  1. Familiarize Yourself with ISO 9001:2015:

    • Get a copy of the ISO 9001:2015 standard and read through it to understand the new requirements and changes compared to ISO 9001:2008.

  2. Gap Analysis:

    • Conduct a gap analysis to identify the areas where your current Quality Management System (QMS) aligns with ISO 9001:2015 and where there are gaps that need to be addressed.

  3. Update Documentation:

    • Revise your QMS documentation, including quality manual, procedures, work instructions, and any other documents, to align with the new standard's requirements.

  4. Implement New Requirements:

    • Integrate new elements like risk-based thinking, context of the organization, and interested parties into your QMS.

  5. Training and Awareness:

    • Provide training to employees to ensure they are aware of the changes in the standard and understand their roles in the updated QMS.

  6. Internal Auditing:

    • Conduct internal audits to verify that the updated QMS is effectively implemented and complies with ISO 9001:2015.

  7. Management Review:

    • Review the QMS with top management to ensure it is still suitable, adequate, and effective in achieving organizational objectives.

  8. Engage a Certification Body:

    • Contact a certification body accredited for ISO 9001:2015. They will guide you through the certification process.

  9. External Certification Audit:

    • Schedule and undergo an external certification audit where the certification body will assess your QMS against the requirements of ISO 9001:2015.

  10. Corrective Actions:

  • Address any non-conformities identified during the certification audit and implement corrective actions as necessary.

  1. Receive ISO 9001:2015 Certification:

    • If your organization successfully demonstrates compliance with ISO 9001:2015, you will receive certification to the new standard.

  2. Maintain and Continually Improve:

    • Continually monitor and improve your QMS to ensure it remains effective in meeting customer requirements and organizational objectives.
Remember that the transition deadline from ISO 9001:2008 to ISO 9001:2015 was in September 2018, so it's crucial to complete the transition as soon as possible to maintain your certification status. If you haven't already, it's important to start this process promptly.

Validity of iso 9001 certificate is valid for 3 years.

Looking forward to your enquiry!