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[General] Neueste ISO-9001-Lead-Auditor Pass Guide & neue Prüfung ISO-9001-Lead-Audito

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【General】 Neueste ISO-9001-Lead-Auditor Pass Guide & neue Prüfung ISO-9001-Lead-Audito

Posted at before yesterday 23:47      View：19 | Replies：0        Print      Only Author   [Copy Link] 1#
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PECB QMS ISO 9001:2015 Lead Auditor Exam ISO-9001-Lead-Auditor Prüfungsfragen mit Lösungen (Q20-Q25):20. Frage
Match the process descriptions below to the process names:

Antwort:
Begründung:

Explanation:
A white background with black text Description automatically generated


21. Frage
During a third-party audit of a pharmaceutical organisation (CD9000) site of seven COVID-19 testing laboratories in various terminals at a major international airport, you interview the CD 9000's General Manager (GM), who was accompanied by Jack, the legal compliance expert. Jack is acting as the guide in the absence of the Technical Manager due to him contracting COVID-19.
You: "What external and internal issues have been identified that could affect CD9000 and its quality management system?" GM: "Jack guided us on this. We identified issues like probable competition of another laboratory organisation in the airport, legal requirements on COVID-19 continuously changing, the shortage of competent laboratory analysists, the epidemic declining soon, shortage of chemicals for the analysis. It was quite a good experience." You: "Did you document these issues?" GM: "No. Jack said that ISO 9001 does not require us to document these issues." You: "How did you determine the risks associated with the issues and did you plan actions to address them?" GM: "I am not sure. The Technical Manager is responsible for this process. Jack may be able to answer this question in his absence." Select two options for how you would respond to the General Manager's suggestion:
  • A. I would ask for a different guide instead of the legal compliance expert.
  • B. I would ask to audit the Technical Manager by phone.
  • C. I would ask the consultant to leave the meeting since he is not an employee of the organisation.
  • D. I would not accept the legal compliance expert answering the question.
  • E. I would delay the audit until the return of the technical manager
  • F. I would look for evidence that the actions resulting from the risk assessment had been taken.
Antwort: A,F
Begründung:
According to the ISO 9001:2015 standard, clause 4.1 requires organizations to determine the external and internal issues that are relevant to their purpose and that affect their ability to achieve the intended outcomes of their quality management system. Clause 6.1 requires organizations to plan actions to address the risks and opportunities associated with these issues. These actions must be integrated into the quality management system processes and evaluated for effectiveness.
In this scenario, the General Manager of the pharmaceutical organization has shown a lack of understanding and involvement in the process of identifying and addressing the external and internal issues that affect their quality management system. The General Manager has relied on the legal compliance expert, who is not an employee of the organization, to guide them on this process. The General Manager has also admitted that they did not document these issues, which is contrary to the requirement of retaining documented information on the context of the organization. The General Manager has also delegated the responsibility of determining and planning the actions to address the risks and opportunities to the Technical Manager, who is absent due to COVID-19.
Based on this information, you can respond to the General Manager's suggestion by taking two options:
B: I would ask for a different guide instead of the legal compliance expert: You can request to have a different guide who is an employee of the organization and who is familiar with the quality management system processes and the external and internal issues that affect them. The legal compliance expert may not have the necessary knowledge and authority to answer your questions or provide you with the relevant evidence.
C: I would look for evidence that the actions resulting from the risk assessment had been taken: You can verify whether the organization has implemented and evaluated the actions to address the risks and opportunities associated with the external and internal issues. You can look for evidence such as records of risk analysis, action plans, monitoring and review results, and improvement measures.
These two options would help you to assess the conformity and effectiveness of the organization's quality management system with respect to the requirements of clauses 4.1 and 6.1.

22. Frage
Match the process descriptions below to the process names:

Antwort:
Begründung:

Explanation:
Match the process descriptions below to the process names:
The process by which the accuracy of test equipment is checked against a known standard. = Calibration The process by which a product or service is visually examined to determine conformity to requirements. = Evaluation The process by which data is examined in detail to reach a specific answer or answers. = Analysis The process by which a parameter of a product or service is examined to determine a specific value. = Measurement According to the ISO 9000:2015 - Quality management systems - Fundamentals and vocabulary, the definitions of the process names are as follows:
Calibration: operation that, under specified conditions, in a first step, establishes a relation between the quantity values with measurement uncertainties provided by measurement standards and corresponding indications with associated measurement uncertainties and, in a second step, uses this information to establish a relation for obtaining a measurement result from an indication.
Evaluation: determination of the suitability, adequacy or effectiveness of an object to achieve established objectives.
Analysis: detailed examination of the elements or structure of something.
Measurement: process to experimentally obtain one or more quantity values that can reasonably be attributed to a quantity.
Therefore, the process descriptions can be matched to the process names based on these definitions.
References:
ISO 9000:2015 - Quality management systems - Fundamentals and vocabulary

23. Frage
Which two of the following work documents are not required for audit planning by an auditor conducting a certification audit?
  • A. An evidence sampling strategy
  • B. An audit plan
  • C. A career history of the quality manager
  • D. A checklist
  • E. An organisation's financial statement
  • F. A list of interested parties
Antwort: C,E

24. Frage
You are conducting an audit at a single-site organisation seeking certification to ISO 9001 for the first time.
The organisation manufactures cosmetics for major retailers and the name of the retailer supplied appears on the product packaging. Sales turnover has increased significantly over the past five years.
You are interviewing the new Product Development Manager. You note that a software application called SWIFT is used to help control the product development process.
You have gathered audit evidence as outlined in the table. Match the ISO 9001 clause 8.3 extracts to the audit evidence.

Antwort:
Begründung:

Explanation:
Audit Evidence and Applicable ISO 9001:2015 Clause 8.3 Extracts
* Half of all new products launched in the past 12 months were late. The Product Development Manager explains he has not got enough people on his team to cope with the demand for new products.# ISO 9001 Clause 8.3.2 e) - "...internal resource needs for the design and development of products and services..."
* The Product Development Manager explains many changes are made to cosmetic formulations during product development owing to retailer feedback. Only when confirmed by the retailer is the agreed formulation documented on SWIFT.# ISO 9001 Clause 8.3.5 - "...retain documented information on design and development changes..."
* The Product Development Manager explains that the customer confirms their approval to proceed with a new formulation by email. These emails are kept on SWIFT.# ISO 9001 Clause
8.3.6 - "...retain documented information on design and development outputs..."
* The Product Development Manager shows you evidence of consumer trials that are carried out for some new products before a full-scale launch.# ISO 9001 Clause 8.3.4 d) - "...conducted to ensure that the resulting products and services meet the requirements..."
* The Product Development Manager explains that an approved external laboratory is used to perform shelf-life stability trials on some formulations during product development.# ISO 9001 Clause 8.3.2 e) - "...external resource needs for the design and development of products and services..." ISO 9001:2015 Clause 8.3 (Design and development of products and services) requires organisations to plan, control, review, verify, validate, and document design and development activities to ensure products meet requirements.
Explanation of clause alignment:
* Clause 8.3.2 e) requires the organisation to determine both internal and external resource needs.
Lack of personnel causing late launches directly evidences internal resource shortfalls, while the use of an external laboratory demonstrates control of external resources.
* Clause 8.3.5 requires organisations to control design and development changes and retain documented information describing those changes, which is demonstrated by controlled updates in SWIFT following retailer confirmation.
* Clause 8.3.6 requires retention of documented information on design and development outputs, including customer approvals, which are evidenced by stored emails in SWIFT.
* Clause 8.3.4 d) requires design and development activities such as verification and validation, ensuring outputs meet requirements. Consumer trials prior to launch clearly meet this requirement.
ISO-aligned conclusion:
The evidence provided demonstrates structured control of product design and development, including planning, resourcing, change management, validation, and retention of documented information, all mapped directly to ISO 9001:2015 Clause 8.3 requirements.

25. Frage
......
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