NZQA registered unit standard / 8084 version 8
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Title / Audit quality management systems for compliance with quality standards
Level / 6 / Credits / 14
Purpose / People credited with this unit standard are able to: prepare to carry out a quality audit; carry out technical aspects of a quality audit; carry out interpersonal aspects of a quality audit; report on a quality audit; and verify corrective actions.
Classification / Business Operations and Development > Quality Management
Available grade / Achieved

Explanatory notes

1Although not prerequisites, Unit 8086, Demonstrate knowledge required for quality auditing, and Unit 8085, Demonstrate knowledge of quality and its management containuseful underpinning knowledge for this unit standard.

2Definitions

Quality is the degree to which a set of inherent characteristics of products and services fulfils the stated and implied requirements of customers and other stakeholders.

Quality management is a philosophy of management that encompasses quality management systems, customer focus, and a consultative culture. The purpose is to continuously improve the value of goods and services to internal and external customers, with outcomes of improved business results and greater effectiveness and efficiency in day-to-day activities.

Quality management systems refers to a formal management system that establishes policy and objectives (and ways of achieving them) in order to direct and control an organisation with regard to quality.

Quality audit is a systematic and independent examination to determine whether quality activities and related results comply with planned arrangements and whether these arrangements are implemented effectively and are suitable to achieve objectives.

Auditee is the organisation, or part thereof, that is to be audited.

Client is the person or organisation requesting the audit. The client can also be the auditee.

Quality standards are the criteria against which the auditee's performance will be audited. Examples of such standards may include but are not limited to, as relevant to the auditee:

AS/NZS 4801:2001: Occupational Health and Safety Management standards – Specification with guidance for use;

other AS/NZS standards;

ACC Partnership Programme: Audit standards (Wellington: Accident Compensation Corporation, 2002), available at

ISO standards;

codes of practice;

any other criteria that have been agreed in the supplied scope of the audit. These can include auditee's plans, procedures, and quality objectives.

3All activities must comply with: any policies, procedures, business protocols, and requirements of the organisation(s) involved; ethical codes and standards of relevant professional bodies; the cultural requirements of the organisation(s) and individuals involved; and any relevant legislative and/or regulatory requirements. Activities must also comply with any guidelines for quality management systems auditing, and any other special conditions pertaining to the industry being audited.

4Legislation relevant to this unit standard can include but is not limited to: Health and Safety in Employment Act 1992, Resource Management Act 1991, Official Information Act 1982, Privacy Act 1993, State Sector Act 1988, Employment Relations Act 2000, Fair Trading Act 1986, Consumer Guarantees Act 1993, and subsequent amendments.

5This unit standard can be applied to both internal and external audits, and to both compliance audits and audits conducted for the purpose of identifying opportunities for improvements.

6The unit standard focuses on the process, not the scope. Candidates must complete at least one full workplace audit (either internal or external) that includes all processes for each outcomeof this unit standard. They will work from a supplied audit scope and plan. The audit may be completed individually or as part of a team.

Outcomes and evidence requirements

Outcome 1

Prepare to carry out a quality audit.

Evidence requirements

1.1Review of auditee's previous audits establishes possible impacts on the conduct of the current audit.

1.2Auditor's individual plan of activities matches the requirements of the supplied audit plan and enables the objectives of the audit to be met.

1.3Assembly and production of working papers ensure collection of the required evidence.

Rangeworking papers may include but are not limited to – checklists, quality standards, organisation charts, previous audit reports, quality system documentation.

Outcome 2

Carry out technical aspects of a quality audit.

Evidence requirements

2.1Audit objectives, audit process, and availability of resources are confirmed with the auditee before the auditing activities begin.

2.2Comparison of the quality standards with the auditee's plans for meeting the standards ensures that variances can be recognised.

2.3The auditing of auditee's performance against plans for these activities ensures that variations can be recognised.

2.4Audit observations are recorded in sufficient detail to ensure that the subsequent analysis can be carried out to the requirements of the supplied audit scope and plan.

2.5Comparisons of observations against auditee's plans and procedures, and against the quality standards, enable compliance or non-compliance to be determined.

2.6Evaluative decisions are made on the basis of sufficient and verifiable evidence so that the extent of compliance and opportunities for improvement can be identified.

2.7Any contingencies that occur during audit are managed to ensure that the integrity of the audit is not compromised.

Rangecontingencies may include but are not limited to – dangerous and critical situations, incapacity of auditor to continue, significant failure of auditee's systems and/or equipment.

2.8Any actions taken as a result of the auditee's responses to findings while the audit is in process do not compromise the integrity of the audit.

Outcome 3

Carry out interpersonal aspects of a quality audit.

Evidence requirements

3.1Audit activities facilitate the co-operation of the auditee, the resolution of conflict, and the communication of all information required to meet the audit objectives.

3.2Communication with the auditee and (if applicable) client ensures that all parties remain informed of the progress of the audit and of any circumstances that could alter planned arrangements.

3.3Communication with any other participating auditors ensures the coordination of audit activities, the consistency of audit performance, and the completion of the audit plan.

3.4All communications with auditees and (if applicable) other auditors demonstrate respect, courtesy and cultural sensitivity.

Outcome 4

Report on a quality audit.

Evidence requirements

4.1Reports identify the extent of compliance with quality standards and areas requiring corrective action to ensure compliance, and include recommendations for improvement where such advice does not compromise the independence of the auditor.

Rangepreliminary report presented at exit interview, final report.

4.2The presentation of the preliminary report covers the required scope, reflects all conclusions, findings, and observations, and ensures that the results of the audit are clearly understood by the auditee.

4.3Negotiation at exit interview establishes auditee's agreement regarding how, when, and by whom corrective actions are to be carried out to achieve compliance with quality standards.

4.4Final audit report is consistent with the preliminary report and negotiated outcomes of the exit interview.

4.5Reports are distributed in accordance with the requirements of the audit plan.

Outcome 5

Verify corrective actions.

Evidence requirements

5.1The evidence gathered is sufficient for an assessment of whether corrective actions have been completed.

5.2Status of corrective actions is reported to client in accordance with negotiated requirements.

5.3Where compliance is not achieved, renegotiation with auditee establishes additional corrective action required to achieve compliance.

Planned review date / 31 December 2019

Status information and last date for assessment for superseded versions

Process / Version / Date / Last Date for Assessment
Registration / 1 / 31 August 1996 / 31 December 2016
Revision / 2 / 7 September 1999 / 31 December 2016
Revision / 3 / 12 January 2001 / 31 December 2016
Review / 4 / 22 September 2004 / 31 December 2016
Rollover and Revision / 5 / 18 July 2008 / 31 December 2016
Rollover and Revision / 6 / 17 November 2011 / 31 December 2016
Rollover and Revision / 7 / 18 April 2013 / 31 December 2018
Rollover / 8 / 16 April 2015 / N/A
Consent and Moderation Requirements (CMR) reference / 0113

This CMR can be accessed at

Please note

Providers must be granted consent to assess against standards (accredited) by NZQA, before they can report credits from assessment against unit standards or deliver courses of study leading to that assessment.

Industry Training Organisations must be granted consent to assess against standards by NZQA before they can register credits from assessment against unit standards.

Providers and Industry Training Organisations, which have been granted consent and which are assessing against unit standards must engage with the moderation system that applies to those standards.

Requirements for consent to assess and an outline of the moderation system that applies to this standard are outlined in the Consent and Moderation Requirements (CMR). The CMR also includes useful information about special requirements for organisations wishing to develop education and training programmes, such as minimum qualifications for tutors and assessors, and special resource requirements.

Comments on this unit standard

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NZQA National Qualifications Services
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