When food companies pursue IFS (International Featured Standards) certification, they place their trust in certification bodies and auditors to conduct thorough, unbiased assessments of their food safety systems. But who ensures these gatekeepers themselves meet rigorous standards? The answer lies in a structured framework of requirements that certification bodies and auditors must satisfy before they can evaluate any food facility.

Table of Contents

The foundation: ISO/IEC 17065 accreditation

Certification bodies operating within the IFS framework must first secure formal accreditation. Originally known as EN 45011, this requirement has been replaced by ISO/IEC 17065:2012, which establishes international standards for bodies certifying products, processes, and services. This accreditation demonstrates that a certification body operates according to globally recognized quality benchmarks.

The accreditation process examines multiple operational aspects. Certification bodies need ISO/IEC 17065 accreditation to become IFS partners, with requirements detailed in Part 3 of all IFS standards. The process scrutinizes organizational structure, ensuring clear responsibility delineation and governance systems that prevent conflicts of interest. It also evaluates management systems, requiring documented procedures for handling applications, conducting audits, and issuing certificates.

Contractual obligations with IFS

Beyond accreditation, certification bodies must enter into contractual agreements with the IFS governing body. These agreements outline scope limitations, defining which IFS standards and industry sectors the certification body is qualified to audit. They also establish financial obligations, reporting protocols for communicating audit results and certificate issuance, and compliance requirements with specific IFS methodologies.

Building auditor competence from the ground up

IFS maintains strict requirements for individuals who conduct certification audits. Auditors need relevant education, experience, language competence, and specific knowledge within product and technology scopes. The qualification pathway ensures that only thoroughly prepared professionals can assess food facilities.

Educational and professional prerequisites

Prospective IFS auditors typically need a food-related university degree combined with at least two years of professional experience in the food industry related to food production activities. This foundation ensures auditors understand the practical realities of food manufacturing, not just theoretical concepts.

Beyond formal education, auditors must demonstrate substantial audit experience. The standard requirement includes 10 complete audits performed at different sites within the past two years, with a maximum of three audits per site. These audits must involve GFSI-recognized standards or retailer audits, ensuring candidates have exposure to rigorous food safety assessment methodologies.

The examination process

Once candidates meet basic qualifications, they must complete initial training provided by their certification body. Following this preparation, they face a comprehensive examination system. Candidates must pass the relevant IFS exam and complete a witnessed sign-off audit before receiving final approval.

The IFS provides various resources through its Auditor Qualification Platform, including the IFS Auditor Toolbox which contains materials to support the approval process. Examination schedules are published annually, with written exams conducted remotely and oral examinations for specific standards like IFS Food and Logistics.

Maintaining competence through continuous development

Initial qualification represents just the beginning of an auditor’s professional journey. IFS requires ongoing demonstration of skills and knowledge to maintain audit eligibility. This approach ensures auditors stay current with evolving food safety challenges and regulatory changes.

Activity requirements

Once approved, auditors can conduct audits until the end of the second calendar year, with approval reviewed bi-annually. To maintain their status, auditors must perform at least five audits per year. This minimum activity level ensures auditors maintain practical skills and stay familiar with real-world food safety operations.

Mandatory training commitments

Continuing education forms a critical component of auditor maintenance requirements. Auditors must attend their certification body’s annual two-day in-house training, which typically covers standard updates, technical developments, and assessment methodology refinements.

Additionally, auditors must participate in bi-annual two-day calibration training provided by IFS. These calibration sessions ensure auditors worldwide assess companies consistently, maintaining uniformity in how IFS standards are interpreted and applied across different regions and food sectors.

Performance monitoring mechanisms

Regular assessment of auditor performance helps maintain quality standards throughout the certification system. Certification bodies must conduct witness audits, where supervisors or accreditation body representatives observe auditors during actual assessments. This oversight occurs at least once every two years, providing direct evaluation of auditor competence and adherence to methodology.

Report reviews constitute another quality check, with certification bodies examining audit documentation for thoroughness and accuracy. Client feedback mechanisms also factor into performance evaluation, considering auditee perspectives on audit conduct and outcomes.

Ethical standards and impartiality requirements

Technical competence alone cannot ensure audit integrity. IFS auditors must adhere to strict ethical standards that preserve the certification process’s credibility and protect all stakeholders in the food supply chain.

Managing conflicts of interest

Auditors must avoid any conflicts of interest, bias, or influence that may compromise audit integrity or validity. This requires formal conflict declarations, where auditors disclose any existing or previous relationships with audit clients that could affect objectivity.

Cooling-off periods apply when auditors have previously provided consulting services to organizations they might later audit. These restrictions prevent situations where auditors might be perceived as auditing their own work or maintaining financial relationships that could compromise professional judgment.

Confidentiality and professional conduct

Auditors must respect the confidentiality and privacy of auditees and audit information. Team members involved in certification must agree to operate ethically with no conflict or perceived conflict of interest, with contractual obligations to disclose potential conflicts allowing for mitigation measures.

Professional accountability extends to honest reporting of findings, regardless of commercial pressures. Auditors must provide truthful assessments even when those findings may result in certification delays or corrective action requirements for the audited facility.

Quality assurance within certification bodies

Certification bodies themselves must implement robust internal quality management systems. These systems include regular internal audits assessing the certification body’s own compliance with IFS requirements, management reviews evaluating system effectiveness and identifying improvement opportunities, and corrective action mechanisms addressing non-conformities within the certification body’s operations.

These quality assurance mechanisms help maintain consistency and reliability across all certification activities, regardless of which individual auditor performs the assessment. The goal is ensuring that an IFS certificate means the same thing whether issued by one certification body or another, in one country or another.

Evolving requirements for emerging challenges

As food safety challenges evolve, so do requirements for certification bodies and auditors. Recent trends include increased specialization, with growing demand for sector-specific expertise beyond general food safety knowledge. Technology integration is expanding competency requirements to include digital verification tools and remote auditing capabilities.

Food fraud emphasis has brought enhanced training on vulnerability assessment and mitigation techniques for emerging intentional adulteration risks. From 2026/27 onwards, AI will play a key role in auditor calibration training, with new modules on artificial intelligence use in auditing and food safety, preparing auditors for future industry challenges.

What do you think? How might emerging technologies like AI change the auditor qualification landscape in the coming years? Does the rigorous qualification process give you confidence in the IFS certification system, or do you see areas where requirements could be strengthened further?

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References
  1. https://www.bioagricert.org/en/from-en-45011-to-iso-17065/
  2. https://www.ifs-certification.com/en/partner-network/certification-bodies
  3. https://www.ifs-certification.com/en/auditors
  4. https://www.linkedin.com/advice/0/what-key-skills-qualifications-food-safety-auditor
  5. https://fsns.com/fsns-certification-audit-services/
  6. https://www.ifs-certification.com/index.php/en/?view=article&id=113%3Acertificatin-bodies

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Food Safety and Quality Management Systems

1 Introduction to Management systems

  1. Introduction to ISO 9001
  2. ISO 9000
  3. Introduction to ISO 14001:2004
  4. How to Use ISO 14001
  5. Introduction to OHSAS 18001:2007
  6. How to Use OHSAS 18001:2007
  7. Introduction to ISO/IEC 27001
  8. The PDCA Model

2 Auditing

  1. Clause 1 – Scope of the Standard
  2. Clause 2 – Normative References
  3. Clause 3 – Terms and Definitions
  4. Clause 4 – Principles of Auditing
  5. Clause 5 – Managing an Audit Program
  6. Clause 6 – Audit Activities
  7. Clause 7 – Competence and Evaluation of Auditors

3 Standardization and Accreditation

  1. International Accreditation Forum (IAF)
  2. International Laboratory Accreditation Cooperation (ILAC)
  3. Quality Council of India (QCI)
  4. National Accreditation Board for Testing and Calibration Laboratories (NABL)
  5. ISO/TS 22003:2007 Food Safety Management System
  6. ISO Guide 65: General Requirements for Bodies Operating Product Certification Systems
  7. ISO/IEC 17020:1998 General Criteria for the Operation of Various Types of Bodies Performing Inspections
  8. ISO/IEC 17021:2006 – Conformity Assessment-Requirements for Bodies Providing Audit and Certification of Management Systems
  9. ISO 17025:2005 General Requirements for the Competence of Testing and Calibration Laboratories

4 ISO 9001-2000 – An Overview

  1. ISO 9000
  2. Quality Management Principles
  3. ISO 9000:2005, Quality Management Systems: Fundamentals and Vocabulary
  4. ISO 9001:2000, Quality Management Systems: Requirements
  5. Steps for Implementing Quality Management Systems
  6. Benefits of ISO 9001:2000
  7. ISO 9004:2000, Quality Management Systems: Guidelines for Performance Improvements
  8. Relationship with ISO 9001:2000
  9. Self-assessment Model

5 ISO 9001-2000 – Structure

  1. Documentation Structure of ISO 9001:2000
  2. Quality Manual
  3. Mandatory Procedures
  4. Standard Operating Procedures (SOPs)
  5. Process Definition Documents
  6. Work Instructions
  7. Miscellaneous Documents
  8. Formats and Records
  9. ISO 9001:2000 Clauses

6 Clause wise interpretation of ISO 9001-2000

  1. Clause 1: Scope
  2. Clause 2: Normative Reference
  3. Clause 3: Terms and Definitions
  4. Clause 4: Quality Management System
  5. Clause 5: Management Responsibility
  6. Clause 6: Resource Management
  7. Clause 7: Product Realization
  8. Clause 8: Measurement, Analysis and Improvement

7 ISO 9001-2000 – Case Studies

  1. Engineering Job Work Organisation
  2. Software Development Organisation
  3. Management Review in Engineering
  4. Customer-Related Processes in Software
  5. Internal Audits in Engineering
  6. Design and Development in Software
  7. Corrective and Preventive Actions in Software
  8. Customer Property Management in Engineering

8 ISO 22000-2005 – An Overview

  1. What Does ISO 22000 Bring to the HACCP Method?
  2. System Components
  3. Communication between Participants in the Food Industry
  4. ISO 22000: A Passport for Exporting?
  5. Why do Companies Commit themselves to an ISO 22000 Approach?
  6. Who Should Use ISO 22000:2005?
  7. Why Use ISO 22000:2005?
  8. ISO 22000 and HACCP
  9. Codex Alimentarius
  10. Key Elements and Benefits of ISO 22000

9 ISO 22000-2005 – Structure

  1. Economic Loss due to Food Borne Illness
  2. ISO 22000: 2005 Clauses
  3. FSMS Documentation Structure
  4. Food Safety Team Structure
  5. Food Safety Manual
  6. Mandatory Procedures
  7. Standard Operating Procedures (SOP)/Work Instructions
  8. HACCP Pre-steps Related Documents
  9. HACCP Principles Related Documents
  10. Miscellaneous Documents
  11. Formats and Records

10 Clause-wise interpretation of ISO 22000- 2005

  1. Clause 1: Scope
  2. Clause 2: Normative References
  3. Clause 3: Terms and Definitions
  4. Clause 4: Food Safety Management System
  5. Clause 5: Management Responsibility
  6. Clause 6: Resource Management
  7. Clause 7: Planning and Realization of Safe Products
  8. Clause 8: Validation, Verification and Improvement of the FSMS

11 ISO 22000-2005-Case Studies

  1. Kick-off meeting
  2. Introduction to the standard
  3. Formation of food safety team
  4. Description of product and its intended use
  5. PRP (Pre-requisite programme)
  6. Flow diagrams, process steps and control measures
  7. Control measure assessment
  8. Verification of food safety management system
  9. Traceability system
  10. External communication
  11. Internal communication
  12. Management Reviews

12 An Overview and Requirements of ISO 17025

  1. Introduction to the ISO/IEC 17025 Standard
  2. Scope of ISO/IEC 17025
  3. Normative References
  4. Terms and Definitions
  5. General Requirements
  6. Structural Requirements
  7. Resource Requirements
  8. Process Requirements
  9. Management System Requirements

13 Requirements specific to Food testing laboratories – Physical and chemical Parameters

  1. Introduction
  2. Quality and Safety Requirements of Food Products
  3. Chemical and Physical Testing Requirements of Food Products
  4. Laboratory Quality Management System
  5. Management Requirements (Clause 4 of ISO 17025)
  6. Technical Requirements (Clause 5 of ISO 17025)
  7. Traceability of Measurement
  8. Sampling
  9. Handling Test and Calibration Items
  10. Assuring the Quality of Test and Calibration Results

14 Requirements specific to Food testing laboratories – Biological parameters

  1. Introduction
  2. Quality and Safety Requirements of Food Products
  3. Biological Testing Requirements of Food Products

15 General topics- related to Food testing laboratories

  1. Method Validation
  2. Ruggedness
  3. Uncertainty of Measurement
  4. International Accreditation Aspects

16 BRC Food and BRC/IOP Standards – An Overview

  1. BRC Global Standard – Food (Issue 5, January 2005)
  2. Introduction to BRC Food Standard
  3. Legislative Requirements
  4. Benefits of the BRC Global Standard – Food
  5. Principles of the BRC Global Standard – Food
  6. The Standard Technical Advisory Committee
  7. Scope of the BRC Global Standard – Food
  8. The Format of the BRC Global Standard – Food
  9. Application
  10. Structure and Interpretation of the Standard
  11. BRC / IOP Global Standard Issue 3 2001 (Food Packaging and Other Packaging Materials)
  12. IOP: The Institute of Packaging
  13. BRC/IOP Relationship
  14. Benefits of BRC/IOP Packaging Standard
  15. Principles of BRC/IOP Packaging Standard
  16. Application
  17. Structure of BRC / IOP Global Standard – Food Packaging and Other Packaging Materials

17 International Food Standard

  1. Background of the IFS
  2. Service Protocol of the IFS ISSUE 5
  3. Contractual Arrangements – Selection of Certifying Body
  4. Audit Notification
  5. Scope of the Audit
  6. Audit Flow – Preparing the Audit Plan
  7. Level Determination – KO, Major NC’s, NA
  8. Scores, Issuing the Audit Report and Certification
  9. Audit Frequency
  10. Audit Report
  11. Awarding of Certificate
  12. Distribution of the Audit Report
  13. Supplementary Action
  14. Appeal Procedure
  15. Complaints
  16. IFS – Catalogue of Requirements
  17. Management of Quality System
  18. Management Responsibility
  19. Resource Management
  20. Product Realization
  21. Measurements, Analysis and Improvements
  22. Requirements for Certification Bodies and Auditors
  23. Report

18 SQF 1000 And SQF 2000

  1. SQF 1000
  2. Interpretation of SQF 1000 Standard
  3. SQF 2000
  4. Interpretation of SQF 2000 Standard
  5. Let Us Sum Up

19 Global GAP and India GAP

  1. Potential Benefits and Challenges Related to Good Agricultural Practices (GAP)
  2. Description of the FAO/GAPs
  3. USDA GAP/GHP Programme
  4. Global GAP
  5. India GAP