EXAM ISO-9001-LEAD-AUDITOR VOUCHER & ISO-9001-LEAD-AUDITOR RELIABLE EXAM SIMULATIONS

Exam ISO-9001-Lead-Auditor Voucher & ISO-9001-Lead-Auditor Reliable Exam Simulations

Exam ISO-9001-Lead-Auditor Voucher & ISO-9001-Lead-Auditor Reliable Exam Simulations

Blog Article

Tags: Exam ISO-9001-Lead-Auditor Voucher, ISO-9001-Lead-Auditor Reliable Exam Simulations, ISO-9001-Lead-Auditor Visual Cert Test, ISO-9001-Lead-Auditor Certification Exam Cost, ISO-9001-Lead-Auditor Exam Braindumps

It is a truth universally acknowledged that the exam is not easy but the related ISO-9001-Lead-Auditor certification is of great significance for workers in this field, I am glad to tell you that our company aims to help you to pass the ISO-9001-Lead-Auditor examination as well as gaining the related certification in a more efficient and simpler way. During nearly ten years, our ISO-9001-Lead-Auditor Exam Questions have met with warm reception and quick sale in the international market. Our ISO-9001-Lead-Auditor study materials are not only as reasonable priced as other makers, but also they are distinctly superior.

If you want to pass the ISO-9001-Lead-Auditor exam, you should buy our ISO-9001-Lead-Auditor exam questions to prapare for it. Our sincerity stems from the good quality of our ISO-9001-Lead-Auditor learning guide is that not only we will give you the most latest content. Also we will give you one year's free update of the ISO-9001-Lead-Auditor Study Materials you purchase and 24/7 online service. Now just make up your mind and get your ISO-9001-Lead-Auditor exam braindumps!

>> Exam ISO-9001-Lead-Auditor Voucher <<

Use PECB ISO-9001-Lead-Auditor Dumps To Deal With Exam Anxiety

There are a lot of experts and professors in our company. All ISO-9001-Lead-Auditor study torrent of our company are designed by these excellent experts and professors in different area. We can make sure that our ISO-9001-Lead-Auditor test torrent has a higher quality than other study materials. The aim of our design is to improving your learning and helping you gains your ISO-9001-Lead-Auditor Certification in the shortest time. If you long to gain the certification, our QMS ISO 9001:2015 Lead Auditor Exam guide torrent will be your best choice.

PECB QMS ISO 9001:2015 Lead Auditor Exam Sample Questions (Q101-Q106):

NEW QUESTION # 101
Select six of the activities that are specifically required by ISO 17021-1 as part third-party (Certification Body) surveillance audit processes.

  • A. Review the calibration status of the instrumentation.
  • B. Review the status of previously raised findings and audit effectiveness of any outstanding findings.
  • C. Audit use of certification marks on marketing materials.
  • D. Review changes to the QMS since last visit.
  • E. Failing to meet financial responsibilities.
  • F. Conduct a minimum number of annual surveillance audits during the certification period.
  • G. Verify legal compliance.
  • H. Handling of customer complaints since last visit.
  • I. Confirm effectiveness of internal audit and management review.
  • J. Complete a full document review of the quality management system.

Answer: B,C,D,G,H,I

Explanation:
The activities that are specifically required by ISO 17021-1 as part of third-party (Certification Body) surveillance audit processes are:
*Option A: Audit use of certification marks on marketing materials. This option is correct because ISO 17021-
1:2015 clause 9.6.2.2 requires the certification body to audit the client's use of marks and/or any other reference to certification, as applicable, to ensure conformity with the certification requirements.
*Option B: Review changes to the QMS since last visit. This option is correct because ISO 17021-1:2015 clause 9.6.2.2 requires the certification body to review any changes affecting the client's quality management system and its ability to continue to fulfil the requirements of the standard used for certification.
*Option C: Confirm effectiveness of internal audit and management review. This option is correct because ISO 17021-1:2015 clause 9.6.2.2 requires the certification body to confirm the continuing effectiveness of the client's quality management system, including the effectiveness of the internal audit and management review processes.
*Option F: Review the status of previously raised findings and audit effectiveness of any outstanding findings.
This option is correct because ISO 17021-1:2015 clause 9.6.2.2 requires the certification body to review the status of findings and any corrective actions taken by the client in response to previous audits, and to verify the effectiveness of the implemented corrective actions.
*Option H: Verify legal compliance. This option is correct because ISO 17021-1:2015 clause 9.6.2.2 requires the certification body to verify the client's compliance with applicable statutory and regulatory requirements related to the scope of certification.
*Option I: Handling of customer complaints since last visit. This option is correct because ISO 17021-1:2015 clause 9.6.2.2 requires the certification body to review the client's handling of customer complaints related to the certified activities since the last audit.
The following options are not correct:
*Option D: Complete a full document review of the quality management system. This option is not correct because ISO 17021-1:2015 clause 9.6.2.2 does not require the certification body to complete a full document review of the quality management system during surveillance audits. A full document review is only required during the initial certification audit or when there are significant changes to the quality management system or the certification requirements.
*Option E: Failing to meet financial responsibilities. This option is not correct because ISO 17021-1:2015 clause 9.6.2.2 does not require the certification body to audit the client's financial responsibilities during surveillance audits. The certification body may have contractual arrangements with the client regarding the payment of fees, but this is not part of the surveillance audit process.
*Option G: Review the calibration status of the instrumentation. This option is not correct because ISO 17021-
1:2015 clause 9.6.2.2 does not require the certification body to review the calibration status of the instrumentation during surveillance audits. The certification body may audit the client's monitoring and measuring resources as part of the quality management system requirements, but this is not a specific activity required by ISO 17021-1.
*Option J: Conduct a minimum number of annual surveillance audits during the certification period. This option is not correct because ISO 17021-1:2015 clause 9.6.2.2 does not require the certification body to conduct a minimum number of annual surveillance audits during the certification period. The certification body may determine the frequency and duration of surveillance audits based on the risk and performance of the client, but this is not a specific activity required by ISO 17021-1.
References:
*ISO 17021-1:2015 Conformity assessment - Requirements for bodies providing audit and certification of management systems - Part 1: Requirements
*ISO 9001 Lead Auditor Course Material, Module 7: Audit Follow-up and Surveillance, Slide 8: Surveillance Audit
*ISO 9001 Lead Auditor Training Course - IRCA Certified, Section 7.2: Audit Follow-up and Surveillance
*Lead Auditor Exam Preparation Guide (EPG) Template - PECB, Section 3.2: Exam Content Outline, Subsection 3.2.1: Section 1 - Audit Fundamentals, Subsection 3.2.2: Section 2 - Audit Principles, Subsection
3.2.3: Section 3 - Audit Process, Subsection 3.2.4: Section 4 - Audit Competencies


NEW QUESTION # 102
Noitol is an organisation specialising in the design and production of e-learning training materials for the insurance market. During an ISO 9001 audit of the development department, the auditor asks the Head of Development about the process used for validation of the final course design. She states that they usually ask customers to validate the product with volunteers. She says that the feedback received often leads to key improvements.
The auditor samples the design records for a recently completed course for the 247 Insurance organisation.
Design verification was carried out but there was no validation report. The Head of Development advises that this customer required the product on an urgent basis, so the validation stage was omitted. When asked, the Head estimates that this occurs about 50% of the time. She confirms that they always ask for feedback and often make changes. There is no record of feedback in the design file for the course.
The auditor decides to review the training course design process in more depth.
Select three options that provide a meaningful audit trail for this process.

  • A. How is technical content of courses verified as correct?
  • B. How is the tutor trained to deliver the completed course?
  • C. How is customer feedback integrated into the course?
  • D. How are students advised about prior learning requirements?
  • E. How is the cost of the course calculated?
  • F. What risks and opportunities have been notified to interested parties?
  • G. What are the qualifications of the administrative staff?
  • H. How is design documentation controlled and managed?

Answer: A,C,H

Explanation:
According to clause 8.3 of ISO 9001:2015, the organization should establish, implement, and maintain a design and development process that is appropriate to ensure the subsequent provision of products and services. The design and development process should include the following activities:
*Determining the requirements for the products and services to be designed and developed, considering the intended use, the statutory and regulatory requirements, the customer and other relevant interested parties' needs and expectations, and the potential risks and opportunities.
*Defining the design and development objectives, stages, responsibilities, and authorities, and ensuring the availability of adequate resources and competence.
*Implementing design and development controls, such as reviews, verification, and validation, to ensure that the design and development outputs meet the design and development inputs, and to identify and resolve any problems or errors.
*Maintaining documented information on the design and development inputs, outputs, reviews, verification, validation, and changes, and ensuring the traceability and conformity of the products and services to the requirements.
*Managing the design and development changes, by identifying, reviewing, and controlling them, and evaluating their effects on the products and services and the QMS.
In this case, the evidence statements that provide a meaningful audit trail for the design and development process are B, E, and F, because they relate to the design and development controls, the documented information, and the verification activities that are required by the standard. These options can help the auditor to assess the effectiveness and conformity of the design and development process, and to identify any nonconformities or opportunities for improvement. The other options are not directly related to clause 8.3, although they may be relevant for other aspects of the QMS, such as clause 7.2 on competence, clause 7.3 on awareness, clause 7.4 on communication, clause 8.2 on requirements for products and services, clause 8.4 on externally provided processes, products, and services, and clause 8.7 on control of nonconforming outputs.
References: ISO 9001:2015, ISO 9001 Auditing Practices Group Guidance on Design and Development, ISO
9001 Clause 8.3 Design and development of products and services


NEW QUESTION # 103
A Health Trust has contracted with Servitup, a catering services organisation which has been certified to ISO
9001 for 1 year. It provides services to ten, small rural
hospitals in remote locations involving purchase and storage of dry goods and fresh produce, preparing meals and loading heated trolleys for ward service by hospital staff. An auditor is conducting the first sole surveillance audit at one site with the Deputy Catering Manager (DCM).
At the closing meeting attended solely by the DCM, the auditor informs him that he has found numerous gaps in the QMS processes which lead him to consider recommending suspension of the organisation's certification. He is particularly concerned with the evidence that patient health is being adversely affected by produce stored beyond its safe consumption date, poor kitchen hygiene and undercooked meals. The DCM says that he cannot make any decisions about these issues in the absence of the Catering Manager due to illness but will write everything down and report to the Catering Manager.
Which two actions should you take in the context of the audit?

  • A. Call the individual(s) managing the audit programme to explain the situation and recommend immediate suspension of certification to protect the integrity of the Certification Body.
  • B. Thank the DCM for his time and express an expectation that improvements will be made in the QMS.
  • C. Recommend that all personnel should be given urgent in-depth training in the QMS.
  • D. Continue with the meeting, present the audit conclusions and inform the DCM that the organisation will receive the audit report in due course.
  • E. Close the meeting immediately after the DCM's response and advise that the issues will be addressed at the next surveillance visit.
  • F. Conclude the meeting early and advise that it will be rescheduled once the Catering Manager has returned to work.

Answer: A,D

Explanation:
The actions that should be taken in the context of the audit are:
*Option B: Call the individual(s) managing the audit programme to explain the situation and recommend immediate suspension of certification to protect the integrity of the Certification Body. This option is correct because the auditor has found serious and significant gaps in the QMS processes that affect the health and safety of the patients, which is a major nonconformity that may warrant suspension of certification. The auditor should inform the individual(s) managing the audit programme of the situation and the audit findings, and recommend immediate suspension of certification to protect the integrity of the Certification Body and the credibility of the certification scheme. The auditor should also follow the Certification Body's procedures and rules for suspension of certification and communicate the decision and the consequences to the auditee.
*Option C: Continue with the meeting, present the audit conclusions and inform the DCM that the organisation will receive the audit report in due course. This option is correct because the auditor should not terminate or postpone the closing meeting due to the absence of the Catering Manager, as the DCM is the auditee's nominated representative for the audit. The auditor should continue with the meeting, present the audit conclusions and the audit findings, and inform the DCM that the organisation will receive the audit report in due course. The auditor should also explain the audit outcome recommendation and the suspension of certification, and request the DCM to acknowledge the receipt and understanding of the audit results.
The following options are not correct:
*Option A: Close the meeting immediately after the DCM's response and advise that the issues will be addressed at the next surveillance visit. This option is not correct because the auditor should not close the meeting without presenting the audit conclusions and the audit findings, as this would violate the audit principles of fairness and transparency. The auditor should also not advise that the issues will be addressed at the next surveillance visit, as this would imply that the auditor is accepting the auditee's delay and inaction, and that the auditor is not taking the major nonconformity seriously.
*Option D: Conclude the meeting early and advise that it will be rescheduled once the Catering Manager has returned to work. This option is not correct because the auditor should not conclude the meeting early or reschedule it due to the absence of the Catering Manager, as this would disrupt the audit process and the audit schedule. The auditor should also not wait for the Catering Manager to return to work, as this would delay the communication and resolution of the major nonconformity, and potentially compromise the health and safety of the patients.
*Option E: Recommend that all personnel should be given urgent in-depth training in the QMS. This option is not correct because the auditor should not recommend or prescribe specific corrective actions to the auditee, as this would violate the audit principles of independence and objectivity. The auditor should only report the audit findings and the audit outcome recommendation, and leave the responsibility and authority for determining and implementing the corrective actions to the auditee.
*Option F: Thank the DCM for his time and express an expectation that improvements will be made in the QMS. This option is not correct because the auditor should not thank the DCM for his time and express an expectation that improvements will be made in the QMS, as this would imply that the auditor is satisfied and optimistic with the auditee's performance and response, and that the auditor is not taking the major nonconformity seriously. The auditor should instead express the concern and dissatisfaction with the auditee's QMS processes and the impact on the health and safety of the patients, and communicate the suspension of certification and the need for urgent and effective corrective actions.
References:
*ISO 19011:2018 Guidelines for auditing management systems, Clause 6.4.2: Conducting audit activities, Subclause k) and l)
*ISO 9001 Lead Auditor Course Material, Module 5: Conducting an Audit, Slide 20: Closing Meeting
*ISO 9001 Lead Auditor Training Course - IRCA Certified, Section 5.5: Closing Meeting
*Lead Auditor Exam Preparation Guide (EPG) Template - PECB, Section 3.2: Exam Content Outline, Subsection 3.2.1: Section 1 - Audit Fundamentals, Subsection 3.2.2: Section 2 - Audit Principles, Subsection
3.2.3: Section 3 - Audit Process, Subsection 3.2.4: Section 4 - Audit Competencies


NEW QUESTION # 104
The following are stages of an audit, put them in the order they would be conducted.

Answer:

Explanation:

Explanation:

Establishing the audit programme objectives
Determining and evaluating the audit programme risks and opportunities
Establishing the audit programme
Initiating the audit
Preparing all audit activity
Conducting the audit activities
To complete the sequence, you can drag and drop the options to the appropriate blank section.
Here is a brief explanation of each stage:
Establishing the audit programme objectives: This is the first stage of the audit process, where the purpose, scope, and criteria of the audit programme are defined. The audit programme objectives should be aligned with the strategic direction and policies of the organization, and should address the needs and expectations of the interested parties12.
Determining and evaluating the audit programme risks and opportunities: This is the second stage of the audit process, where the factors that can affect the achievement of the audit programme objectives are identified and assessed. The audit programme risks and opportunities should consider the internal and external issues, the requirements and changes of the interested parties, and the results and feedback from previous audits12.
Establishing the audit programme: This is the third stage of the audit process, where the audit programme is designed and implemented. The audit programme should include the audit programme procedures, the audit programme resources, the audit methods and techniques, the audit frequency and schedule, and the audit programme performance indicators12.
Initiating the audit: This is the fourth stage of the audit process, where the audit is prepared and planned. The audit initiation involves selecting the audit team, establishing the contact with the auditee, defining the audit objectives, scope, and criteria, developing the audit plan, and conducting the document review123.
Preparing all audit activity: This is the fifth stage of the audit process, where the audit activities are organized and coordinated. The audit preparation involves assigning the audit tasks, communicating with the auditee and the audit team, arranging the logistics, preparing the working documents, and conducting the opening meeting123.
Conducting the audit activities: This is the sixth and final stage of the audit process, where the audit evidence is collected and evaluated. The audit conduct involves performing the audit activities, such as interviews, observations, document reviews, and tests, documenting the audit findings, preparing the audit conclusions, and conducting the closing meeting123.
I hope this helps you with your ISO 9001 Lead Auditor objectives and content. If you have any further questions, please feel free to ask.
References: 1: ISO 19011:2018 - Guidelines for auditing management systems 2: Audit Process | Flowchart | Summary - Accountinguide 3: What are the Stages of the Auditing Process & Why it is Important ...


NEW QUESTION # 105
XYZ Corporation is an organisation that employs 100 people. As audit team leader, you are conducting a certification audit at Stage 1. When reviewing the quality management system (QMS) documentation, you find that quality objectives have been set for every employee in the organisation except top management.
The Quality Manager complains that this has created a lot of resistance to the QMS, and the Chief Executive is asking questions about how much it will cost. He asks for your opinion on whether this is the correct method of setting objectives.
Three months after Stage 1, you return to XYZ Corporation to conduct a Stage 2 certification audit as Audit Team Leader with one other auditor. You find that the Quality Manager has cancelled the previous quality objectives for all employees and replaced them with a single objective for himself. This states that "The Quality Manager will drive multiple improvements in the QMS in the next year". The Quality Manager indicates that this gives him the authority to issue instructions to department managers when quality improvement is needed. He says that this approach has the full backing of senior management. He shows you the latest Quality Improvement Request that was included in the last management review.

After further auditing, the issues below were found. Select three statements that apply to the term 'audit trail'

  • A. Quality improvements not aligning with the quality policy.
  • B. Limited knowledge of the content of Quality Improvement Requests by departmental staff.
  • C. Top management claim not to be aware of the improvement request (QI/12/20/HR-3) initiated by the Quality Manager.
  • D. Decisions on improvement action timescales not involving departmental managers.
  • E. The single quality objective set for the organisation by the Quality Manager.
  • F. Evaluation of the results of the improvement action not always documented by the Quality Manager.

Answer: B,D,F

Explanation:
Based on the scenario and the concept of an 'audit trail' within the context of ISO 9001, the three statements that apply would likely be:
A: Decisions on improvement action timescales not involving departmental managers. This indicates a lack of involvement and communication with those responsible for implementing the improvements, which is a key part of an effective audit trail1.
B: Evaluation of the results of the improvement action not always documented by the Quality Manager.
Proper documentation is essential for an audit trail, as it provides evidence that actions have been evaluated and are effective1.
C: Limited knowledge of the content of Quality Improvement Requests by departmental staff. An audit trail should ensure that all relevant parties are aware of and understand the actions being taken, which is not the case here1.
These points suggest issues with the communication, documentation, and involvement of relevant personnel in the quality management system processes, which are crucial for maintaining an effective audit trail and, by extension, a robust quality management system.


NEW QUESTION # 106
......

One of the key factors for passing the exam is practice. Candidates must use ISO-9001-Lead-Auditor practice test material to be able to perform at their best on the real exam. This is why FreePdfDump has developed three formats to assist candidates in their ISO-9001-Lead-Auditor Preparation. These formats include desktop-based ISO-9001-Lead-Auditor practice test software, web-based practice test, and a PDF format.

ISO-9001-Lead-Auditor Reliable Exam Simulations: https://www.freepdfdump.top/ISO-9001-Lead-Auditor-valid-torrent.html

We guarantee the pass rate of ISO-9001-Lead-Auditor dumps actual test is up to 99%, Maybe you want to keep our ISO-9001-Lead-Auditor exam guide available on your phone, If you want to pass real tests and stand out, ISO-9001-Lead-Auditor dump collection will assist examinees to get through the examination easily, More importantly, the examination pass rate of FreePdfDump ISO-9001-Lead-Auditor Reliable Exam Simulations is highest in the worldwide, If you are finding a study material in order to get away from your exam, you can spend little time to know about our ISO-9001-Lead-Auditor test torrent, it must suit for you.

And he covers a wide range of methods, from managing just a handful of devices to dealing with hundreds, Applying patches to the OS as needed, We guarantee the pass rate of ISO-9001-Lead-Auditor Dumps actual test is up to 99%.

Three Formats for PECB ISO-9001-Lead-Auditor Exam Questions

Maybe you want to keep our ISO-9001-Lead-Auditor exam guide available on your phone, If you want to pass real tests and stand out, ISO-9001-Lead-Auditor dump collection will assist examinees to get through the examination easily.

More importantly, the examination pass rate ISO-9001-Lead-Auditor of FreePdfDump is highest in the worldwide, If you are finding a study material in order to get away from your exam, you can spend little time to know about our ISO-9001-Lead-Auditor test torrent, it must suit for you.

Report this page