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In 2026, a failed attempt costs more than pride — it costs the exam fee and the weeks spent preparing. PrepAwayETE protects both with 268 practice questions for the ISO-9001-Lead-Auditor日本語 exam and a free demo so you can verify the quality first.
PECB ISO-9001-Lead-Auditor日本語 Exam Overview:
| Certification Vendor: | PECB |
|---|---|
| Exam Name: | PECB Certified ISO 9001:2015 Lead Auditor Examination |
| Exam Number: | ISO 9001 Lead Auditor Exam |
| Related Certifications: | ISO 19011 Lead Auditor ISO 9001:2015 Foundation ISO 9001:2015 Lead Implementer QMS ISO 9001:2015 Internal Auditor |
| Real Exam Qty: | 80 MCQs |
| Exam Price: | Varies by region (typically approx. USD 500–800) |
| Available Languages: | Portuguese, German, Arabic, Chinese, Spanish, English, French |
| Certificate Validity Period: | 3 years (renewal required for certification validity) |
| Exam Format: | Multiple Choice Questions, Closed-book exam, Scenario-based questions |
| Passing Score: | 70% |
| Exam Duration: | 180 minutes |
| Recommended Training: | PECB ISO 9001 Lead Auditor Training ISO 9001:2015 QMS Training Resources |
| Exam Registration: | PECB Exam Registration Portal PECB Official Certification Page |
| Sample Questions: | DOWNLOAD DEMO |
| Exam Way: | Online proctored or onsite exam (depending on PECB authorized providers) |
| Pre Condition: | Recommended: basic knowledge of ISO 9001:2015 or prior experience in quality management systems or auditing. |
| Official Syllabus URL: | https://pecb.com |
PECB ISO-9001-Lead-Auditor日本語 Exam Syllabus Topics:
| Section | Objectives |
|---|---|
| Quality Management System (QMS) Fundamentals | - Quality Principles
|
| Audit Planning and Preparation | - Audit Preparation
|
| Audit Reporting and Follow-up | - Audit Reporting
|
| Conducting Audit Activities | - On-site Audit Execution
|
| Audit Principles and Fundamentals | - Auditor Competence
|
ISO-9001-Lead-Auditor日本語 Preparation: Your Questions Answered
Many candidates combine practice questions with official training. Recommended options include:
This package includes 268 practice questions for the PECB QMS ISO 9001:2015 Lead Auditor Exam (ISO-9001-Lead-Auditor日本語版) exam. Every answer is verified by an experienced team of experts, so you can trust what you study.
Yes. The online test engine runs entirely in a web browser, which is why it works identically on Windows, Mac, Android, and iOS without any installation. If you can open a browser, you can practice — on a computer at home or a phone on the move.
The PECB QMS ISO 9001:2015 Lead Auditor Exam (ISO-9001-Lead-Auditor日本語版) exam contains 80 MCQs questions, and you will have 180 minutes minutes to complete them. Simulating this exact combination during practice builds both speed and accuracy.
The PECB QMS ISO 9001:2015 Lead Auditor Exam (ISO-9001-Lead-Auditor日本語版) exam requires a score of 70% to pass, and the official registration fee is Varies by region (typically approx. USD 500–800). Thorough preparation is the most reliable way to protect that investment.
You can register for the PECB QMS ISO 9001:2015 Lead Auditor Exam (ISO-9001-Lead-Auditor日本語版) exam through the official channels:
The PC test engine installs on Windows and runs on a standard Java environment, which most computers already have or can add in minutes. Once installed, it simulates the real exam scenario with timed sessions, automatic scoring, and mistake tracking — a full practice lab on your own computer.
The PECB QMS ISO 9001:2015 Lead Auditor Exam (ISO-9001-Lead-Auditor日本語版) practice questions are organized around the official exam objectives. Key topics include:
- Conducting Audit Activities ()
- Audit Principles and Fundamentals ()
- Audit Planning and Preparation ()
Coverage follows the official syllabus, so your practice time always maps to exam content.
Recommended: basic knowledge of ISO 9001:2015 or prior experience in quality management systems or auditing.
You can confirm the current eligibility requirements on the official ISO-9001-Lead-Auditor日本語 exam page before you register.
PECB QMS ISO 9001:2015 Lead Auditor Exam (ISO-9001-Lead-Auditor日本語版) Sample Questions:
組織のパフォーマンスに関連して、ISO 9001 の品質管理システムの目的を最もよく表すフレーズを選択してください。
- A. パフォーマンスが向上します
- B. パフォーマンスを監視する
- C. パフォーマンスを管理する
- D. パフォーマンスを決定
Correct Answer: A 🗳️
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XYZ 社は 100 人の従業員を抱える組織です。監査チームのリーダーとして、ステージ 1 の認証監査を実施します。品質管理システム (QMS) を確認すると、外部コンサルタントが競合他社の目標を参考にして目標を定義しているものの、文書化されていないことがわかりました。品質管理者は、このことが QMS に対する大きな抵抗を生み出していると不満を述べ、最高経営責任者はコストがいくらかかるのかを尋ねています。
ISO 9001 の条項 6.2 に対して不適合を指摘できる状況を説明する 2 つのオプションはどれですか。
- A. 組織は品質目標を一度にすべて達成する余裕がありません。
- B. 品質目標は組織の品質方針に沿って設定されていませんでした。
- C. 品質目標が組織の担当者によって実行されていません。
- D. コンサルタントは ISO 9001 を正しく解釈していません。
- E. 品質目標は文書化された情報として維持されていません。
- F. 品質目標の設定に経営トップは関与していませんでした。
Correct Answer: B,E 🗳️
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(監査中に不適合を報告する場合、次の項目のうちどの 2 つを不適合ステートメントに含める必要がありますか?)
- A. 不適合の責任者(監査対象者)の名前
- B. 監査基準の説明または参照
- C. 不適合の存在を確認した監査チームの技術専門家の名前
- D. 不適合を排除するために被監査者が実施しなければならない行動
- E. 是正措置を実施する目標時期
- F. 関連する監査証拠
Correct Answer: B,F 🗳️
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サードパーティ監査の次の手順を、実行される正しい順序に並べます。
Correct Answer:

Explanation:
Sequence:
Stage 1 Audit
Stage 2 Opening Meeting
Interviews
Stage 2 Closing Meeting
Close-out of Stage 2 Audit Findings
Issue Certificate
Surveillance Audit
Follow-up Audit
To complete the sequence, you can drag and drop the options to the appropriate blank section.
Here is a brief explanation of each step:
Stage 1 Audit: This is the initial audit that aims to assess the readiness of the organization for the stage 2 audit. It involves reviewing the documentation of the quality management system, evaluating the scope and objectives of the audit, and identifying any major gaps or nonconformities34.
Stage 2 Opening Meeting: This is the meeting that marks the start of the stage 2 audit. It involves confirming the audit plan, the audit criteria, the audit scope, and the audit team. It also provides an opportunity for the auditee to ask any questions or raise any concerns34.
Interviews: This is the main activity of the stage 2 audit, where the audit team collects evidence by interviewing the personnel involved in the quality management system, observing the processes and activities, and examining the records and documents. The audit team uses various techniques, such as sampling, measurement, analysis, and evaluation, to verify the conformity and effectiveness of the quality management system345.
Stage 2 Closing Meeting: This is the meeting that marks the end of the stage 2 audit. It involves presenting the audit findings, the audit conclusions, and the audit report to the auditee. It also provides an opportunity for the auditee to provide feedback, ask questions, or dispute any findings34.
Close-out of Stage 2 Audit Findings: This is the process of verifying that the auditee has taken appropriate corrective actions to address any nonconformities or opportunities for improvement identified during the stage
2 audit. The audit team may request evidence or conduct a follow-up visit to confirm the effectiveness of the corrective actions34.
Issue Certificate: This is the process of issuing a certificate of conformity to the auditee, if the audit team is satisfied that the quality management system meets the requirements of the standard and that there are no major nonconformities or unresolved issues. The certificate is valid for a specified period, usually three years, and is subject to periodic surveillance audits34.
Surveillance Audit: This is the process of conducting periodic audits, usually once a year, to monitor the continued conformity and effectiveness of the quality management system. It involves reviewing the changes, improvements, and performance of the quality management system, and identifying any new nonconformities or opportunities for improvement34.
Follow-up Audit: This is the process of conducting an additional audit, usually in response to a significant change, a complaint, or a major nonconformity, to verify the impact and the corrective actions taken by the auditee. It may result in the suspension, withdrawal, or renewal of the certificate, depending on the outcome of the audit34.
あなたは、複数の拠点を持つ組織のステージ 2 認証監査を主導しており、以下の監査スケジュールを受け取りました。本社および拠点 1 - 1 日目、拠点 2 (本社から 150 km) - 2 日目と 3 日目。監査の 1 日目に、クライアントから、作業員の間で深刻な感染症が発生したため、拠点 2 の実験室で除染のための投薬が行われたとの通知がありました。拠点 2 では、他のすべての機能は計画どおりに監査できます。
監査チームのリーダーとして、あなたは何をしますか?
実行できる最善のアクションを選択してください。
監査プログラム マネージャーに指示を依頼します。
3 日目に監査を完了し、認証機関に報告して認証の決定をもらいます。
2 日目と 3 日目に監査を継続し、後ほどサイト 2 の研究所を監査するために戻ります。
監査計画を完了できないため、直ちに監査をキャンセルします。
監査チームに作業を割り当てる責任は誰にありますか?
- A. 認証機関
- B. 監査チームメンバー
- C. 監査対象組織
- D. 監査チームリーダー
Correct Answer: D 🗳️
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