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Book Titles No access
Health, Safety, Environmental, and Quality Auditing
- Authors:
- |
- Publisher:
- 2025
Keywords
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Bibliographic data
- Copyright year
- 2025
- ISBN-Print
- 979-8-89205-046-3
- ISBN-Online
- 979-8-89205-047-0
- Publisher
- Bernan, Lanham
- Language
- English
- Pages
- 466
- Product type
- Book Titles
Table of contents
ChapterPages
- Contents No access
- Acknowledgments No access
- Growth of Regulations No access
- Growth in Visibility No access
- Continuing Enforcement No access
- Impact on the Regulated Community No access
- Defining HSEQ Audits No access
- What’s In a Name? An Audit by Any Other Name Is Still an Audit No access
- The Continuing Evolution of Guidelines and Standards No access
- Incorporating Security and Social Responsibility No access
- Conducting Supply Chain Audits No access
- Conducting Third-Party Audit Program Evaluations No access
- Improving International HSEQ Audits No access
- The Use of Digital/Cell Phone Cameras No access
- References No access
- Example: Canadian Offshore Oil and Gas Industry No access
- Audits and Safety Inspections No access
- References No access
- Introduction No access
- Function of HSEQ Audits No access
- Role of HSEQ Audits in Regulatory Compliance No access
- Practical Considerations and Recommendations for Performing Self-Assessments No access
- References No access
- Principles of an Audit Program No access
- Establishing an HSEQ Audit Policy or Procedure No access
- Program Objectives for HSEQ Audits No access
- Roles and Responsibilities No access
- Legal Protections No access
- Scope and Coverage No access
- Regulatory Differences to Be Reflected in Quality Audit—Example 1 No access
- Project Quality Auditing No access
- Project Auditing Process No access
- Project Audit Schedule No access
- Regulatory Differences to Be Reflected in Quality Audit—Example 2 No access
- Facility Audit Schedules No access
- Auditor Selection and Training No access
- Audit Reports and Documentation No access
- Audit Program Management and Evaluation No access
- Audit Program Support Tools No access
- HSEQ Record-Keeping/Records-Retention Procedures No access
- External Regulatory Inspection Procedures No access
- Continuous Review No access
- Evaluating the Results and Implementing the Solutions No access
- References No access
- Introduction No access
- ISO 45001 No access
- Development No access
- Certification No access
- ISO 45001 changes compared to OHSAS 18001 No access
- Voluntary Public Reporting No access
- Third-Party Program Evaluations and Certifications No access
- Benchmarking Studies No access
- References No access
- Program Name No access
- Purpose No access
- Program Organization No access
- Program Scope No access
- Audit Methodology No access
- Reporting of Findings No access
- Follow-Up Mechanisms No access
- Audit Staffing No access
- Audit Duration No access
- Number of Facilities Audited per Year No access
- Frequency of Audits No access
- Conclusion No access
- References No access
- 1. Precisely Define the Scope No access
- 2. Select Target Companies Using a Variety of Techniques No access
- 3. Create Participation Incentives No access
- 4. Develop Measurable Criteria No access
- 5. Utilize Focus Group Sessions No access
- Best Practices No access
- Reports to Management No access
- Relationship to Compensation No access
- Emergency Response No access
- Next-Site Participation No access
- Use of Laptop and Tablet Computers, Intranets, and the Internet No access
- Assessment of Ancillary Operations No access
- Use of Verification Audits No access
- Site-Satisfaction Questionnaire No access
- Periodic Third-Party Evaluations No access
- Development of an Audit Program News or Chat Group No access
- Biggest Challenges No access
- The Program Manual No access
- Integrated HSEQ Management System Checklist No access
- Part 1: Context of the Organization No access
- Part 2: Leadership. Leadership and Commitment No access
- Part 3: Planning. Actions to Address Risks and Opportunities No access
- Part 4: Support No access
- Part 5: Operation No access
- Part 6: Performance Evaluation No access
- Part 7: Improvement No access
- Integrated Audit Checklist No access
- Detailed Audit Checklist Sections No access
- ISO 9001:2015 Specific Checklist Points No access
- ISO 14001:2015 Specific Checklist Points No access
- ISO 45001:2018 Specific Checklist Points No access
- Additional References from Standards No access
- Impact of ChatGPT on HSEQ Auditing No access
- How ChatGPT Can Be Used by Professional HSEQ Auditors No access
- Practical Examples No access
- Future Developments No access
- Jurisdictional Regulatory Review No access
- Unclear or Unknown Corporate Standards No access
- Misleading Closing Meeting and Conferences No access
- Timeliness and Quality of the Audit Report No access
- Insufficient Follow-Up No access
- Lack of Program Metrics No access
- References No access
- The Need No access
- Competency Framework No access
- Selecting the Trainers No access
- Selecting the Trainees No access
- Selecting the Setting No access
- Lecture No access
- Keys to Making It Work No access
- Characteristics and Qualifications of Good Auditors No access
- The Worst Attributes No access
- The Best Attributes No access
- Making Good Things Happen No access
- Conclusion No access
- References No access
- 1. Explicit Top-Management Support No access
- 2. Program and Auditor Independence No access
- 3. Appropriate Audit Team Staffing No access
- 4. Comprehensive Written Audit Procedures No access
- 5. Defined Program Objectives and Scope No access
- 6. Adequate Program Resources No access
- 7. Audit Frequency Based on Risk No access
- 8. Documented Audit Process No access
- 9. Documentation of Audit Findings No access
- 10. Resolution of Corrective Actions No access
- 11. Appropriate Quality-Assurance Measures No access
- How Are the Evaluations Conducted? No access
- References No access
- Regulatory Databases No access
- Commercially Available Audit Protocols No access
- Advantages No access
- Disadvantages No access
- HSEQ Audit Software—Information Management Databases No access
- Control of Documented Information (Documents and Records) No access
- Confessions of a Vice President of HSEQ Management System Software No access
- Audit Management Technology No access
- Customer Communication and Feedback No access
- HSEQ Software—Modules and Processes No access
- Defining Your Functional Needs for HSEQ Software No access
- 1. HSE Compliance Module Essential Features No access
- 2. Internal Audit and Inspection Module Essential Features No access
- 3. Action Management Module Essential Features No access
- 4. General Considerations No access
- Comparing Two Integrated Quality and Safety Management Systems: QMS versus SMS No access
- Do You Have Too Many Software Systems? No access
- About Q5 and Quality Management Systems No access
- Some Quality Software Programs Have Evolved No access
- Better Integrated Quality and Safety Management Software No access
- Final Thoughts on Integrated Quality and Safety Management Systems No access
- E-Auditing: Beware Pencil Whipping (or Digital Smartphone or Tablet Whipping) No access
- Traditional Responses to HSEQ Audit Document Management No access
- The Advantages of Integrated Data-Management Systems No access
- Evaluating Auditing Software Systems No access
- References No access
- 1. Develop an HSEQ Audit Policy and Procedure No access
- 2. Set Up the Organization No access
- 3. Develop Tools No access
- 4. Train Staff No access
- 5. Test the Program No access
- 6. Set a Review Schedule No access
- 7. Conduct Audits No access
- 8. Implement the Full Program No access
- Assessment Tools No access
- Management Reports No access
- HSEQ Audit Staff Management—Keeping Them Engaged No access
- Quality Assurance No access
- Maintaining Awareness No access
- Conclusion No access
- References No access
- Introduction No access
- Team Selection and Formation No access
- Audit Background No access
- Team Leader Only No access
- All Team Members (Including Team Leader) No access
- Completion and Review of the Preaudit Questionnaire No access
- Review of Relevant Regulations No access
- Definition of Audit Scope and Establishment of Team Responsibilities No access
- Development of a Detailed Audit Agenda or Plan No access
- Review of Audit Protocols No access
- Arrange Logistics No access
- On-Site Activities No access
- Orientation Tour No access
- Overview of Management Systems and the Organization No access
- Records/Documentation Review No access
- Schedule Interviews Ahead of Time (If Possible) No access
- Conduct Interviews in the Workspaces No access
- Be Sensitive to the Interviewee’s Nervousness and Defensiveness No access
- Avoid Closed-ended Yes/No Responses to Questions No access
- Be Open to Follow-Up Interviews with Other Staff No access
- Preparing for the Closing Conference No access
- Conducting the Closing Conference No access
- References No access
- 1. Take Charge of the Meeting No access
- 2. Be Organized No access
- 3. Discuss Logistics No access
- 4. Find Out What’s Happening at the Site No access
- 5. Schedule Additional Conferences No access
- 6. Address Important Topics No access
- 1. Take Charge of the Meeting No access
- 2. Be Organized No access
- 3. Be Appreciative but Do Not Bury the Message No access
- 4. Set Priorities No access
- 5. Minimize Praise for “Acceptable” Performance No access
- 6. Respond Professionally to Challenges No access
- 7. Focus on Root Causes but Avoid Evaluations of Staff Performance No access
- 8. Understand How to Handle Repeat Findings No access
- 9. Avoid Comparisons No access
- 10. Avoid Guarantees or Absolutes No access
- 11. Leave Some Form of Written Findings (If You Can) No access
- 12. Discuss the Next Steps No access
- 13. Solicit Site Feedback No access
- References No access
- Keep the Customer in Mind No access
- Look for Underlying Causes No access
- Organize Daily No access
- Pinpoint the Bottom Line of Interviews No access
- Develop an Annotated Outline No access
- Challenge Each Other No access
- Develop a Consistent Debriefing Approach No access
- Organize for Monitoring No access
- Start Early No access
- Establish a Report Format No access
- Pay Attention to Repeat Findings No access
- Be Careful of Good Management Practices or Opportunities for Improvement (OFI) No access
- Set Priorities No access
- Be Clear and Concise No access
- Deemphasize Numbers No access
- Use Evidence in the Discussion of Findings No access
- Assure Legal Review of Reports where Required No access
- Limit Distribution of the Report No access
- Accept No Mistakes No access
- Remove Barriers to Efficiency No access
- Develop Action Plans No access
- Train the Auditors No access
- References No access
- Develop and Maintain a “Living” Agenda throughout the Audit No access
- You Will Never Finish, so Manage Your Time Wisely No access
- Keep a Balance between Records Review, Interviews, and Observation No access
- “Things” Will Happen on the Audit, so Be Flexible No access
- Always Be on Time, Even When the Facility Staff Are Not No access
- Remember Site Staff Will Always Consider Audits a Performance Evaluation No access
- Remember That Despite the Existence of Governmental Regulations and Company Policies, Procedure or ISO Standards, Considerable Judgment Is Still Required No access
- Remember That Every Country, State, Province, and Region Is Different No access
- Learn and Apply the Audit Protocols, but Do Not Forget to Use Your Common Sense and Natural Curiosity No access
- Try to Observe Things as They Happen No access
- Observe Ancillary Operations (If Possible) No access
- Observe, Articulate, and Write—in That Order No access
- Remember That Writing Is the Hardest Part; Developing “Bulletproof” Findings Is an Elusive Goal No access
- Write the Findings as You Go No access
- Prepare Well for the Opening and Closing Conferences No access
- Make Sure the Facility Hears the Real Story in the Closing Conference No access
- Plan to Be Done When You Depart No access
- Enjoy Yourself No access
- References No access
- Key On-Site Activities No access
- Failure to Understand How Much Time Is Actually Available No access
- Poorly Designed Audit Agendas No access
- Failure to Focus Full Attention on the Audit No access
- Failure to Schedule Time Needed to Produce On-Site Deliverables No access
- Improper Sample Size No access
- Lack of Auditor Independence in Verification Activities No access
- Lack of Field Verification No access
- Poor Balance among Records Review, Interviews, and Observations No access
- Disorganized Records Review No access
- Poor Interviewing Techniques No access
- Poor Finding Communication No access
- Poorly Structured Closing Conferences No access
- The Top Three Things to Remember No access
- References No access
- Statement of Observation No access
- Statement of Requirement No access
- Citation or Regulatory Reference No access
- Regulatory Findings No access
- Policy and Procedure Findings No access
- Guidance/Observation Findings No access
- Commendations No access
- Finding Level No access
- Recommendation (Corrective Action/Preventive Action) No access
- Audit “Findings Forms” or Templates No access
- Vague Observation Statements No access
- No Statement of Requirement No access
- Lack of Citations or Applicable Regulatory References No access
- Overly Stringent Priority Classifications No access
- Other Challenges and Pitfalls No access
- References No access
- Exploring Your Integrated Auditing Opportunities No access
- Sample Content for and Internal Audit Procedure No access
- President (or Other Top-Management Representative) No access
- Managers and Supervisors No access
- Employees and Staff No access
- Audit Initiation No access
- Frequency of Audits No access
- Internal HSEQ Auditor Qualifications and Training No access
- Audit Planning, Scheduling, and Preparing for Audits No access
- Opening Meeting No access
- Conducting the Audit No access
- Reporting Audit Results No access
- Audit Action Plan No access
- Audit Findings Analysis and Review No access
- Auditor (Extreme) Bias—Beware of Registration Auditors Bearing Books No access
- References No access
- Table of Contents No access
- What Is Involved No access
- Auditing Overview No access
- What No access
- Why No access
- When No access
- Where No access
- Who No access
- How to Perform an Audit No access
- Activities Involved in the Audit Process No access
- Inform Participants No access
- The Date(s) of the Audit No access
- The Purpose of the Audit No access
- Who Will Be Involved No access
- The Types of Activities that Will Occur No access
- How Results Will Be Communicated No access
- Locate Necessary Information No access
- Gather Tools No access
- Performing the Audit No access
- Step One: Preaudit Review No access
- Required Training No access
- Audit Instrument Section Pages No access
- Referencing Numbers No access
- Audit Question No access
- Score Weighting No access
- Points Awarded No access
- Audit Guidelines No access
- Documentation Technique No access
- Selecting Documentation No access
- Documentation Types No access
- Assessing Documentation No access
- Dos and Don’ts of Referencing Documentation No access
- Documentation Technique—Review No access
- Purpose No access
- Checklist No access
- Visiting Sites No access
- Interview Technique No access
- Interview Questionnaires (Checklists) No access
- Who Should Be Interviewed? No access
- Selecting Interviewees When On-site No access
- Dos and Don’ts When Conducting an Interview No access
- Communication Skills No access
- Concluding an Interview No access
- Interview Technique—Review No access
- Interview Summary—Using the Interview Response Summary Tool No access
- Observation Summary No access
- Documentation Summary No access
- Check for Accuracy No access
- Analyzing Results No access
- Cor® Executive Summary Sheet No access
- COR® Audit—Corrective Action Plan No access
- Making Recommendations No access
- Close-out Meeting No access
- Personnel Definitions No access
- Other Definitions No access
- Acronyms No access
- ISO 45001:2018 OHS Audit Tool No access
- 1.0Purpose No access
- 2.0Scope No access
- 3.0Audit Schedule No access
- 4.0 Interview List—Potential Interviewees No access
- 5.0 Audit Basis No access
- 6.0 Exit Interview, Closing Meeting, and Action Tracking No access
- 7.0 Reporting/Distribution No access
- 8.0 Documentation Requirements—Pre-Audit No access
- 9.0 Comments or Questions No access
- Contents No access
- What Is an Audit? No access
- Management System Audits No access
- Types of Audits No access
- Process Interaction Flow No access
- Audit Program No access
- Example: Audit Planning Matrix No access
- Audit Schedule No access
- Auditing Principles No access
- Auditors No access
- Who Can Be an Auditor No access
- Team Lead (Lead Auditor) No access
- Auditors No access
- Technical Experts No access
- Observers No access
- Trainees No access
- Phases of an Audit No access
- Initiating the Audit No access
- Audit Objectives No access
- Audit Plan No access
- Audit Checklist No access
- Step 1: Open the Audit No access
- Step 2: Conduct the Audit No access
- Step 3: Close the Audit No access
- Conducting Interviews No access
- What is a Good Question? No access
- Open-Ended Questions No access
- Pointed Questions No access
- Summary No access
- Objective Evidence No access
- Fact versus Inference No access
- Definition of a Fact No access
- Definition of an Inference No access
- Content of the Audit Report No access
- Audit Findings No access
- Noncompliance No access
- Nonconformance No access
- Area of Concern/Risk No access
- Observation No access
- Improvement Opportunity No access
- Positive Observations No access
- Documenting Audit Findings No access
- Example Statement of Nonconformance No access
- Follow-up Audits No access
- Summary No access
- References No access
- ChatGPT-generated integrated HSEQ Audit Checklist No access Pages 441 - 448
- Index No access Pages 449 - 462
- Co-Principal Author—Terri Andrews No access
- Co-Principal Author—Wayne Pardy No access




