In today’s quality-driven global market, the ability to establish, implement, and audit effective quality plans is a competitive advantage. The LICQual ISO 10005:2018 Guidelines for Quality Lead Auditor course is a specialized, internationally recognized training program designed to empower professionals with the competencies required to lead audits focused on quality planning as outlined in the ISO 10005:2018 standard.
ISO 10005:2018 provides guidance on the development and application of quality plans that are tailored to specific products, projects, or contracts. This course enables learners to not only understand the structure and principles of ISO 10005:2018 but also apply audit techniques that assess compliance with these guidelines across various industries. The focus is on quality planning as a strategic tool for improving efficiency, compliance, and customer satisfaction.
Delivered by certified and industry-experienced instructors, the LICQual ISO 10005:2018 Guidelines for Quality Lead Auditor course combines theoretical knowledge with practical audit scenarios. Participants will gain deep insight into auditing processes, from planning and execution to reporting and follow-up, with a clear focus on quality planning effectiveness and integration within quality management systems.
Whether you are an internal auditor, quality manager, project lead, or consultant, this course will strengthen your ability to drive value-added audits that support operational excellence. On successful completion, participants will receive the prestigious LICQual certification, recognized internationally as a benchmark of professional competence in quality planning audits.
The LICQual ISO 10005:2018 Guidelines for Quality Lead Auditor course offers an in-depth exploration of ISO 10005:2018, a standard that provides clear and structured guidance on creating and implementing effective quality plans. This course is tailored for professionals who audit or manage quality planning activities within organizational and project settings, especially where compliance with quality management systems is critical.
Participants will begin by understanding the fundamental concepts, scope, and structure of ISO 10005:2018, including its relationship with ISO 9001 and other quality management standards. Emphasis is placed on how quality plans serve as operational tools to ensure that products, services, and processes meet customer and regulatory requirements.
The course then transitions into auditing practices, where learners will develop the skills needed to assess the adequacy, application, and effectiveness of quality plans. Through case studies, interactive discussions, and audit simulations, participants will learn how to conduct comprehensive audits that verify compliance with ISO 10005:2018 and drive continual improvement.
Key topics include audit planning, risk assessment, evidence collection, nonconformity reporting, and follow-up procedures. The course also delves into the leadership and communication skills necessary to lead audit teams and deliver value-driven audit findings to senior management and stakeholders.
By the end of the program, participants will be fully equipped to lead ISO 10005:2018 audits, recommend improvements to quality planning processes, and contribute to enhanced quality performance across industries. The LICQual ISO 10005:2018 Guidelines for Quality Lead Auditor certification serves as a globally respected credential for professionals committed to excellence in quality management and auditing.
Course Overview
Qualification Title
LICQual ISO 10005:2018 Guidelines for Quality Lead Auditor
Total Units
6
Total Credits
40
GLH
120
Qualification #
LICQ2200408
Qualification Specification
To enroll in the LICQual ISO 10005:2018 Guidelines for Quality Lead Auditor applicants must meet the following criteria:
|
Qualification# |
Unit Title |
Credits |
GLH |
|---|---|---|---|
|
LICQ2200408-1 |
Introduction to ISO 10005:2018 |
8 |
24 |
|
LICQ2200408-2 |
Quality Planning Framework |
8 |
24 |
|
LICQ2200408-3 |
Auditing Quality Management Systems |
6 |
18 |
|
LICQ2200408-4 |
Risk-Based Thinking in Quality Planning |
6 |
18 |
|
LICQ2200408-5 |
Implementation of ISO 10005:2018 |
6 |
18 |
|
LICQ2200408-6 |
Reporting and Documentation |
6 |
18 |
By the end of this course, learners will be able to:
1. Introduction to ISO 10005:2018
- Understand the key objectives and structure of ISO 10005:2018 and its relevance in quality management.
- Recognize the relationship between ISO 10005:2018 and other ISO standards, including ISO 9001.
- Explain the purpose and application of quality planning guidelines in the context of the ISO 10005:2018 standard.
2. Quality Planning Framework
- Identify the components of an effective quality planning framework based on ISO 10005:2018.
- Understand how to integrate quality planning into the overall Quality Management System (QMS).
- Demonstrate the ability to create quality plans that meet the specific needs of products, services, or projects.
3. Auditing Quality Management Systems
- Learn auditing techniques to assess the adequacy and effectiveness of QMS based on ISO 10005:2018 guidelines.
- Develop the skills to perform audits that evaluate quality planning, risk management, and process performance.
- Apply audit methodologies to identify nonconformities and areas for improvement within quality management systems.
4. Risk-Based Thinking in Quality Planning
- Understand the principles of risk-based thinking and its application in quality planning processes.
- Assess how risk management and mitigation strategies are embedded in ISO 10005:2018 quality plans.
- Demonstrate the ability to audit and evaluate the effectiveness of risk-based approaches in quality management.
5. Implementation of ISO 10005:2018
- Develop strategies for implementing ISO 10005:2018 quality planning guidelines within an organization.
- Identify the steps required to align quality planning with organizational goals and customer requirements.
- Demonstrate how to manage the challenges and complexities associated with the implementation of ISO 10005:2018.
6. Reporting and Documentation
- Learn how to document audit findings clearly and effectively, ensuring alignment with ISO 10005:2018.
- Understand the key components of audit reports, including evidence, nonconformities, and corrective actions.
- Develop skills in writing actionable recommendations and communicating audit results to stakeholders.
This diploma is ideal for:
- Quality management professionals aiming to specialize in quality planning and auditing based on ISO 10005:2018 guidelines.
- Internal auditors who wish to gain expertise in auditing quality management systems and quality planning processes.
- Project managers and team leads responsible for developing and implementing quality plans within their organizations.
- Consultants working with organizations to improve quality planning and align practices with ISO standards.
- Engineers, production managers, and operations leaders seeking to understand the integration of quality planning in operational workflows.
- Professionals with prior experience in ISO 9001 or related quality management standards who want to expand their skills in quality planning auditing.
- Individuals pursuing certification to enhance their career opportunities and credentials in the field of quality management and auditing.
Assessment and Verification
All units within this qualification are subject to internal assessment by the approved centre and external verification by LICQual. The qualification follows a criterion-referenced assessment approach, ensuring that learners meet all specified learning outcomes.
To achieve a ‘Pass’ in any unit, learners must provide valid, sufficient, and authentic evidence demonstrating their attainment of all learning outcomes and compliance with the prescribed assessment criteria. The Assessor is responsible for evaluating the evidence and determining whether the learner has successfully met the required standards.
Assessors must maintain a clear and comprehensive audit trail, documenting the basis for their assessment decisions to ensure transparency, consistency, and compliance with quality assurance requirements.
