ISO-9001-Lead-Auditor Exam Dumps - PECB ISO 9001 Questions and Answers

Quality management principles:

Customer focus = Increased revenue and market share

Engagement of people = Enhanced trust and collaboration throughout the organisation

Improvement = Enhanced drive for innovation

Evidence-based decision-making = Increased ability to demonstrate effectiveness of past actions

According to the Quality management principles document published by ISO, each quality management principle has a statement, a rationale, key benefits, and actions you can take to apply it. Based on these descriptions, the potential benefits can be matched to the corresponding principles as follows:

Customer focus: The primary focus of quality management is to meet customer requirements and to strive to exceed customer expectations. The key benefits of this principle include increased customer value, customer satisfaction, customer loyalty, repeat business, reputation, customer base, revenue and market share.

Engagement of people: Competent, empowered and engaged people at all levels throughout the organization are essential to enhance its capability to create and deliver value. The key benefits of this principle include improved understanding of the organization’s objectives and values, increased involvement in improvement activities, enhanced personal development, increased motivation and empowerment, enhanced trust and collaboration, and increased recognition and rewards.

Improvement: Successful organizations have an ongoing focus on improvement. The key benefits of this principle include improved organizational capabilities, alignment of improvement activities at all levels, increased ability to anticipate and react to opportunities and threats, enhanced drive for innovation, and increased levels of satisfaction.

Evidence-based decision-making: Decisions based on the analysis and evaluation of data and information are more likely to produce desired results. The key benefits of this principle include improved decision-making processes, increased ability to demonstrate the effectiveness of past decisions, increased ability to review, challenge and change opinions and decisions, and increased ability to improve performance.

ISO 9001:2015 makes it clear that an organisation remains responsible for conformity to requirements even when processes are outsourced . Certification audits must therefore evaluate not only the organisation’s internal activities, but also the control and effectiveness of externally provided processes .

ISO 9001:2015, Clause 8.4.1 requires that the organisation ensure externally provided processes, products and services conform to requirements. The organisation must determine controls to be applied to those outsourced processes.

ISO 9001:2015, Clause 4.4.1 further requires the organisation to determine processes needed for the quality management system and their application throughout the organisation, including outsourced processes.

For a third-party certification audit , sufficient objective evidence must be obtained to demonstrate that:

Outsourced processes are effectively controlled

The organisation’s quality management system achieves its intended results

Why option C is the best decision:

Proceeding with the audit in Bolivia and including all ABC personnel and all outsourced processes ensures that the certification audit:

Covers the full scope of the QMS , including outsourced production, maintenance, procurement, and HR activities

Allows direct evaluation of how ABC controls and manages its external providers in the location where those processes are actually performed

Provides sufficient objective evidence to support a valid certification decision

Reviewing only internal audits or auditing only planning activities would not provide adequate assurance of conformity for a high-risk, core operational activity such as lithium extraction.

Why the other options are not acceptable:

A : Auditing only the Planning function would exclude core operational and support processes that are within the scope of the QMS.

B : Reviewing internal audit results alone is insufficient for a third-party certification audit and does not replace direct assessment of outsourced processes.

D : ISO 9001 explicitly allows outsourcing of processes; the organisation remains responsible for control, not prohibited from outsourcing.

ISO-aligned conclusion:

In a third-party ISO 9001 certification audit, outsourced processes that are within scope must be audited , either directly or through appropriate controls. In this scenario, auditing the outsourced processes in Bolivia is necessary to ensure a complete, credible, and compliant certification audit.

According to clause 8.4 of ISO 9001:2015, the organization should ensure that externally provided processes, products, and services conform to the specified requirements. To do so, the organization should:

•Establish the criteria for the selection, evaluation, and re-evaluation of external providers, based on their ability to provide processes, products, and services in accordance with the requirements. The criteria should be documented and applied consistently.

•Evaluate the potential external providers before selecting them, using the established criteria. The evaluation methods may include questionnaires, audits, references, samples, etc. The results of the evaluation should be documented and reviewed.

•Select the external providers that have demonstrated their competence and conformity to the requirements. The selection should be based on the evaluation results and the organization’s needs. The selection should be documented and approved.

•Communicate the requirements for the processes, products, and services to be provided by the external provider, including the verification and validation activities, the acceptance criteria, the documentation requirements, the changes control, etc. The communication methods may include purchase orders, contracts, agreements, etc. The communication should be clear, complete, and timely.

•Monitor the performance and conformity of the external provider, using the established criteria and methods. The monitoring methods may include inspections, tests, audits, feedback, complaints, etc. The monitoring results should be documented and analyzed.

In this case, the evidence statements that demonstrate a nonconformity with clause 8.4 are A and C, because they show that the organization did not retain documented information of the selection and evaluation of the external provider, and the monitoring of the external provider’s performance. These are requirements of the standard and essential for ensuring the quality of the externally provided processes, products, and services. The other options are not directly related to clause 8.4, although they may indicate other nonconformities or weaknesses in the organization’s QMS. For example, option B may relate to clause 7.1.3 on contingency planning, option D may relate to clause 8.2.3 on review of requirements, option E may relate to clause 8.6 on release of products and services, and option F may relate to clause 5.1.1 on leadership and commitment. References: ISO 9001:2015, [ISO 9001 Auditing Practices Group Guidance on Scope], Mastering the Scope of ISO 9001 Quality Management Systems

According to ISO 9001:2015, clause 6.2.1, the organization is required to establish quality objectives at relevant functions, levels, and processes for the quality management system (QMS). The quality objectives must be consistent with the quality policy, measurable, monitored, communicated, and updated as appropriate. The organization is also required to maintain documented information on the quality objectives, as per clause 7.5.1.

Therefore, in the scenario given, the quality objectives defined by the external consultant are not in alignment with the organization’s quality policy, as they are based on those of a competitor, rather than the organization’s own purpose, strategic direction, and customer requirements. This creates a mismatch between the organization’s vision and goals, and the quality objectives that are supposed to guide and measure the QMS performance. Moreover, the quality objectives are not maintained as documented information, which makes it difficult to communicate, monitor, and update them, as well as to demonstrate evidence of their implementation and achievement.

Hence, the circumstances in which a nonconformity against clause 6.2 of ISO 9001 could be raised are B and C, as they indicate a failure to comply with the requirements of clause 6.2.1. The other options are either irrelevant or not directly related to clause 6.2, as they do not pertain to the establishment and documentation of quality objectives.

According to ISO 19011:2018, clause 6.3.2, the audit plan is a document that provides the basis for agreement regarding the conduct of the audit. The audit plan should include the following information1:

•the audit objectives, scope and criteria

•the audit team members and their roles and responsibilities

•the audit schedule, including the date, time and location of each audit activity

•the expected time and duration of meetings and interviews

•the allocation of appropriate resources to critical areas of the audit

•the identification of the audit client and the auditee

•the identification of the guides and observers, if any

•the documents and records to be reviewed before and during the audit

•the audit methods and tools to be used

•the audit language and terminology

•the audit report content, format, distribution and expected completion date

•the risk to achieving audit objectives and the contingency plan, if any

Therefore, the issue which is not expected to be included in the audit plan is C, expectations of the organisation’s management. This issue is not relevant to the conduct of the audit, as the audit is based on the audit criteria, not on the management’s expectations. The management’s expectations may be considered during the audit initiation or the audit programme management, but they are not part of the audit plan.

A properly written nonconformity statement should contain:

A clear description of the objective evidence.

Reference to the audit criteria not fulfilled.

Identification of where and when the evidence was found.

Sufficient traceability to allow investigation and corrective action.

Classification/grade where required by the certification body ' s process.

Why B is Correct

If any of the ORANGE+ procedures for bottling and labelling products were not being met.

The nonconformity should reference the specific internal procedure or audit criterion that was not followed.

Why C is Correct

The grade of nonconformity (major or minor).

In certification audits, nonconformities are typically classified according to certification body rules.

Why D is Correct

The date on which the evidence was identified.

The audit record should identify when the evidence was observed.

Why F is Correct

Batch number audited.

The batch number provides traceability and allows the organisation to investigate the affected product.

Why H is Correct

The description of the ISO 9001:2015 requirement not being complied with and the clause number.

A nonconformity must reference the audit criterion that was not fulfilled.

Why I is Correct

The place where the bottles with the wrong label were found.

The location where the evidence was observed should be recorded as part of the objective evidence.

Why the Other Options Are Incorrect

A. The regulatory requirements that apply to the juice being bottled.

May be relevant background information, but it is not essential information required to complete the nonconformity statement.

E. Composition of both sugar and sugarless juices.

Not required to establish the nonconformity.

G. Name of the supervisor and of the workers who were responsible for the bottling process.

Auditors report system failures, not assign blame to individuals.

J. The signature of the M1’s supervisor accepting the non-conformity.

ISO 9001 and ISO 19011 do not require the auditee ' s signature to validate a nonconformity.

ISO-Aligned Conclusion

The six items that should be added to complete the nonconformity report are:

B. If any of the ORANGE+ procedures for bottling and labelling products were not being met.

C. The grade of nonconformity (major or minor).

D. The date on which the evidence was identified.

F. Batch number audited.

H. The description of the ISO 9001:2015 requirement not being complied with and the clause number.

I. The place where the bottles with the wrong label were found.

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