add value So, as part of nonconformity statements have you discovered system nonconformity?



Similar documents
Effective Root Cause Analysis For Corrective and Preventive Action

The three tests of mental ability you will be asked to do at the AOSB are:

COMBINE. Part B. Manual for Marine Monitoring in the. Programme of HELCOM. General guidelines on quality assurance for monitoring in the Baltic Sea

Root Cause Analysis & Systemic Corrective Action

ISO 9001 Quality Management Systems Professional

Auditing HACCP Programs

White paper. Corrective action: The closed-loop system

STEEL fabrication quality SySTEmS guideline

calibrate confidence with Risk Management: The Critical Role of Measurement and Calibration WHITE PAPER SERVICES

Implementing ISO 9001

Internal Audit Checklist

Checklist. Standard for Medical Laboratory

TOTAL QUALITY MANAGEMENT II QUALITY AUDIT

Quality & Safety Manual

PROPOSED DOCUMENT. Quality management system Medical devices Nonconformity Grading System for Regulatory Purposes and Information Ex-change

Module 15: Nonconformance And Corrective And Preventive Action

Specialties Manufacturing. Talladega Castings & Machine Co., Inc. ISO 9001:2008. Quality Manual

Copies of this document shall be classified either as Controlled or Uncontrolled, and shall be identified as such on the cover sheet.


Process Mapping and Process- Based Internal Audits

Lauren Sundararajan, CFE, Internal Audit Manager

AUDITOR GUIDELINES. Responsibilities Supporting Inputs. Receive AAA, Sign and return to IMS with audit report. Document Review required?

preparing a business plan

Certification criteria for. Internal QMS Auditor Training Course

Abu Dhabi EHSMS Regulatory Framework (AD EHSMS RF)

Preparation for a Software Quality Audit

Self-Audit Checklist

Single Manufacturing Site with. Extended Manufacturing Site(s)

ISO 9001 Quality Management Systems. Tips for Internal Auditing

Quality Manual. DuraTech Industries, Inc Commerce Street La Crosse, WI MANUAL SERIAL NUMBER 1

ISO 9001: A Quality Manual for the Transition Period and Beyond

HONG KONG ENVIRONMENTAL ELECTRICAL APPLIANCE COMPANY. Environmental Procedure

The following paragraphs, identified to coincide with the OHSAS 18001:2007 numbering system, provide a clause-by-clause summary of the standard.

UK Aerospace Industry Controlled Other Party (ICOP) Auditor Authentication Scheme

Mapping Your Success Top Non-Conformities Requiring a CAPA Process

DNV GL Assessment Checklist ISO 9001:2015

ISO Registration Guidance Document

ISO 14001:2004 EMS Internal Audit Guidance

Aerospace Guidance Document

ISO 14001:2004 EMS Internal Audit Checklist & Gap Analysis

Company Quality Manual Document No. QM Rev 0. 0 John Rickey Initial Release. Controlled Copy Stamp. authorized signature

Effective Internal Audit Planning:

Quality Management Standard BS EN ISO 9001:

Effective Policy Management White Paper Second Edition updated for Sarbanes-Oxley

Process Streamlining. Whitepapers. Written by A Hall Operations Director. Origins

BUSINESS WRITING BASICS

ISO 9000 Quality Standard Background Information Quality Systems Implementation

1. What types of organisation do you fund? 2. Do you give grants for individual children and young people?

STRENGTHENING SUPPLIER RELATIONSHIPS: WITH COMPREHENSIVE AUDIT PLANING

MEAT GRADING AND CERTIFICATION BRANCH QUALITY MANUAL

D. MCLAUGHLIN & SONS LTD QUALITY MANUAL

WORKPLACE HEALTH AND SAFETY AUDITING GUIDELINES

EMS Example Example EMS Audit Procedure

Jonathan Wilson. Sector Manager (Health & Safety)

HIRING A QUALIFIED OFFICE STAFF

ISO 9001:2008 Internal Audit Guidance

INTEGRATED MANAGEMENT SYSTEM MANUAL IMS. Based on ISO 9001:2008 and ISO 14001:2004 Standards

Guidance from the Group of Notified Bodies for the Construction Products Directive 89/106/EEC. GNB-CPD position paper from SG17 - EN :2009

ISO 9001:2008 Clause PR018 Internal Audit Procedure

ISO 9001:2008 STANDARD OPERATING PROCEDURES MANUAL

FAQ 9101:2014 / 9101E Rev

Cornell Note Taking System (For Lecture or Reading)

QUALITY MANUAL ISO 9001:2015

SUPPLIER QUALITY SYSTEM AUDIT

To be used in conjunction with the Invitation to Tender for Consultancy template.

ISO 9001:2008 Internal Audit & Gap Analysis Checklist

COMPANY NAME. Environmental Management System Manual

Improving Management Review Meetings Frequently Asked Questions (FAQs)

SAMPLE EXAMINATION. If you have any questions regarding this sample examination, please

ISO/IEC Registration Guidance Document

Guide to CQI Qualifications for learners

Quality Meets the CEO

NABET Accreditation Criteria for QMS Lead Auditor Training Course

ISO/IEC QUALITY MANUAL

Evaluation of the Quality System Appraisal of Conformity

GCSE Business Studies. Ratios. For first teaching from September 2009 For first award in Summer 2011

Maintaining employees focus and motivation is essential if they are to make a full contribution to your business.

Design Verification The Case for Verification, Not Validation

Checklist of ISO Mandatory Documentation

What is Lean Manufacturing?

III. Best Practices/Resources

Performance Appraisal

Summary of Requirements for ISO 14001:2004 February 24, 2005

ISO 9001 (2000) QUALITY MANAGEMENT SYSTEM ASSESSMENT REPORT SUPPLIER/ SUBCONTRACTOR

Reading Comprehension questions

Effective complaint handling

ENVIRONMENTAL MANAGEMENT SYSTEM PLANNING GUIDANCE UNDER THE TOXICS USE REDUCTION ACT (TURA)

Five ways to reduce PowerPoint overload

Fundamentals Level Skills Module, F8 (IRL)

JOHN HART GENERATING STATION REPLACEMENT PROJECT. Schedule 9. Quality Management

SUPPLIER QUALITY MANAGEMENT SYSTEM QUESTIONNAIRE

How quality assurance reviews can strengthen the strategic value of internal auditing*

ENGR 1181 Lab 2: Quality and Productivity Lab

SUPPLIER Form #: 007 AUDIT QUESTIONNAIRE

OH&S MANAGEMENT SYSTEM CHECKLIST - AS 4801:2001 (STATUS A = Acceptable; N = Not Acceptable; N/A = Not Applicable)

Requirements- based UAV Design Process Explained

Quality Management System Manual Revision L

Transcription:

s add value Well-crafted s help companies remove the root causes of hidden or neglected costly problems. Much auditee time and money is wasted chasing auditor comments and recommendations often in the guise of s or observations So, as part of their auditor improvement service, Quality Management International are offering an elearning course on their website, www. aworldofquality.com, free of charge. Each has three parts. You can learn how to write each part so together the defines the problem clearly for the corrective action or problem solving team. You can 23 emomentum apr-may07 also learn how to weighup the magnitude of the. N o n c o n f o r m i t y, finding or observation; you can find two of these definitions in ISO 19011 the international standard for auditing management systems. N o n c o n f o r m i t y means nonfulfillment of a requirement. Note that the requirement does not have to be specified or documented. By the way, processes that fail to fulfill their objectives are ineffective. In most cases effectiveness equates to conformity. Work that conforms to an ineffective procedure would not conform to the system standard. A finding used to be called an observation and is a of fact from an audit. The term observation used to mean a of fact from the audit. ISO changed this term to finding in the year 2000 after years of auditors misusing the term observation. Some auditors report observations to impose their will or express their opinion about something they do not like. Unfortunately, so as not to upset their auditor, auditees still accept observations instead of conformity or when their auditor is unsure, lazy or opinionated. have you discovered system? Have you discovered system? When a person, process or product fails to meet a requirement the system is nonconforming in some way. Notice how auditors do not refer to people as nonconformities! Human factors studies following the investigation of air accidents have also concluded that the system causes human error.

Even though auditors look for evidence of conformity they find evidence of. Usually this is the result of their thorough research, focused sampling, keen listening and observing skills although some auditees may think their auditors are just lucky! On finding evidence of discuss the situation with the manager responsible for the area and: 1. Agree the requirement 2. Seek contrary evidence 3. Make notes and evaluate evidence 4. Reach a conclusion 5. Agree the conclusion Never agree with an operator. For example determine the availability of competent operators in discussion with the supervisor not by asking the operator how they know how to do their job! If an operator was not working in conformity with a documented instruction then ask why. You may find they received verbal instructions from a manager that contradicted the documented instruction. Seek a manager responsible for that part of the system. Agree the requirement and the evidence in support of any unusual interpretation of the requirement from the system standard. Ask the manager for any evidence that may contradict the. Update your notes and objectively evaluate whether you have evidence of conformity. Conclude conformity or and discuss the basis for your conclusion with the manager. Be prepared to consider contrary evidence from the auditee. purpose of a The s inform the auditee how the system has failed to meet a requirement and are the starting points for effective corrective action. They are the record on which an auditor bases his or her audit conclusions. Your audit s summary will include a conclusion that answers the question posed by the audit objective. Base your conclusions on the audit findings including the positive points and the nonconformities. You are unlikely to recommend selection of a supplier who operates a system with a major or critical. You are likely to recommend a supplier using a system with a few minor nonconformities. Notice how even with process and product nonconformities you are identifying the part of the system found to be responsible for the. Your clear definition of the problem is essential for the auditee s effective corrective action. Every comprises three parts: the unfulfilled requirement, the supporting evidence and the nature or description of the problem. Requirements are from the audit criteria, for example: Clause reference of system standard Auditee s management system Auditee manager s Contract Regulation Specification The auditee knows the audit criteria from the beginning of the audit. Do not surprise the auditee with new criteria. These are the client-specified or auditor-recommended requirements necessary to support the audit objective. The requirements (shalls) do not include guidelines (shoulds). Auditors ignore guidelines when reporting conformity or. Auditee management may verbally clarify their requirements during the audit and the auditor uses such requirements as audit criteria if within the scope of the audit. Evidence is verifiable and comes from your 24 emomentum apr-may07

notes, for example: Name or job title of the auditee Statements Name of the process (and core or support) Document references Serial numbers Sample size Time and location Description of the possible consequences of the Do not use hearsay as evidence. Your notes will include the evidence If not then you need to improve your notetaking during the audit. What you or the audit team has not verified directly is hearsay. Record your notes so the auditee can later verify the evidence; keep copies to the extent necessary. Do not use a voice recorder, they are intimidating and inefficient. If you sense a blame culture do not to make matters worse by naming operators in your s. Involve your interviewee in getting an accurate record of their s and of the possible consequences Pay attention to the unique numbers of machines and devices and to the document and revision letters or numbers. Record sizes of samples take and keep all the records at the time of doing the audit. Be prepared to keep rough notes on paper for later updating of the checklist on your laptop. Nature is the opposite of the requirement, some broad examples: Failure to determine the criteria for the marketing process to be effective Failure to monitor and require correction of the design process Failure to collect and analyze supplier performance data repair disposition approval authority document approval design validation Test the evidence against the nature. In other words select the requirement, state the opposite of the requirement and see if the evidence supports the nature If not, you have the wrong requirement or no. The nature of the is a description of the problem. It defines the problem ready for problem solving or corrective action. Alone, these examples may seem broad but with the evidence they become clear. writing the Inform management of the problem, reach agreement and make notes. Decide if corrective action would add value. If so, prepare s before the closing meeting. Expect an auditee-challenge if incorrect. Review all notes, including team members and: State the requirement, evidence and nature Check the, is it correct, complete and clear? Read s aloud (to detect grammatical errors) You will have listened to and examined any evidence contrary to the facts of. You will have reached agreement and have made excellent notes. You will have access to corrective action request forms from your client or the auditee. Now ask yourself if the corrective action is likely to add value. If in doubt discuss and agree this with the lead auditor who may apply the 80:20 rule* and elect to merely note the lesser nonconformities in the audit report. * 80% of the value may come from 20% of the nonconformities! The auditee has a right to reject s that are incorrect, incomplete or unclear even if only slightly contrary to the facts. categorizing nonconformities Sometimes it is useful to categorize nonconformities. For example you may need to know whether to recommend selection of a supplier. So ask the audit client for the major/ minor criteria. More than six examples of the same in the same system may for example indicate a chronic problem or major. Almost all system and process nonconformities would be minor or isolated implementation problems. Some failures to fulfill requirements are more serious than others, for example: 25 emomentum apr-may07

Critical: Chronic/repetitive problem System breakdown Adversely affecting the environment or the customer (core process) Less critical: Isolated implementation problems Support process Write your n o n c o n f o r m i t y only when you are sure that your fellow audit team members did not find contradictory evidence. Write your ensuring that it includes the correct requirement, the evidence that s u b s t a n t i a t e s nonfulfillment of the requirement. Ensure it also describes the nature of the problem. New auditors may write these three parts separately but experienced auditors tend to write one or two sentences that include all three parts. Ask the auditee (or a colleague on the audit team) to check your to ensure that it is correct, complete and clear. You will be reading your aloud in the closing meeting. Read it aloud (even to yourself!) before the meeting when you can correct it without losing credibility. M a n a g e m e n t acknowledging receipt of the s You may obtain the signature of a top manager on a major before the closing meeting. This leader can then prepare to demonstrate his or her commitment to prompt and effective corrective action at the closing meeting. In any case ask the auditee (at least at management representative level) to sign each to acknowledge receipt. You could ask, Would you like a copy? The auditee will answer yes and you can respond with please sign them first. The auditee may get started immediately on determining and removing the root causes. The auditee cannot however claim to have completed the corrective action until they have evidence of effectiveness. summary audit report The auditor s summary report can act as a cover sheet to the s showing the audit objective at the top and audit conclusion at the bottom also identifying the audit team members. It reports the degree of conformity per the audit s criteria, objectives and scope: Areas/processes audited (sample) Positive points (these are findings also) Major/minor nonconformities are you in the loop? click below to check out our media section to get up to date! rabqsa media 26 emomentum apr-may07

examples GOOD, BAD AND UGLY AUDIT REPORTS Nonconformity Statement Example 1 In the Instrument Shop, meter serial number 852, used as a standard to calibrate other meters, was due recalibration 2 months ago, on 25 June. It had not been recalibrated. ISO 9001:2000 - clause 7.6 a) Notice how the auditor was careful to ascertain the use of meter 852. If the calibration record indicted that the meters overdue calibration resulted in a hazard then this evidence may have changed this to a major. Likewise, if calibration is part of the core process. Nonconformity Statement Example 2 Drawing TP 354/88 Issue 4, in use in the Fabrication Shop, had an alteration to a design detail. There was no evidence that this alteration had Design Department approval, as required by the document control procedure PR-QMS-01(03). ISO 9001:2000 - clause 4.2.3 b) Even though this is part of the core process it is still a minor unless of course the alteration was to a key characteristic or unapproved alterations were chronic. By the way, this is incomplete. It should include a description of the altered design detail. Nonconformity Statement Example 3 The wastewater treatment filters were not replaced every summer as specified in the preventive maintenance plan. Purchasing records and the WW Supervisor indicated that the last filter replacement was 2 summers ago. Failure to maintain the #1 wastewater treatment plant by replacing filters as planned. ISO 14001:2004 - clause 4.4.6 Again this is part of the core process (even though waste water is a by-product). This is a minor. Had it resulted in significant adverse environmental impact then this additional evidence would have made it a major. 27 emomentum apr-may07 (the nature part of the s) Your conclusion per the audit s objectives. Do not rewrite the nonconformities in the summary. making a mistake Mistakes are learning opportunities. Be quick to recognize a factual error. Correct if you can or remove the from the report and update the audit record. Apologize for your mistake. Lead auditors quickly weigh up the facts and arbitrate decisively. giving advice Provide advisory services only if documented as an audit objective. Do not make the audit client pay for advice when they agreed to pay for audit. If required by the audit client to advise during audit then ensure the documented audit objective includes with consulting or similar. Be careful, advice may weaken the system by making it dependent on its auditors. Advice may also disqualify you from independently auditing that system or part of the system for two years. Auditees who keep asking the auditor for advice may be providing evidence of their ineffective training or corrective action processes. conclusion Value-added audits have encouraged some auditors to provide advice on how to conform to the standard or release information that belongs to their other auditees. Doing so fails to protect the customer s intellectual property and makes the system depend too much on its auditor. W e l l - c r a f t e d n o n c o n f o r m i t y s may be the result of valueadding audits. Such audits focus first on the auditee s core process for converting the needs of stakeholders into cash*. Instead of asking who? auditees ask why? and think system, act on their system and learn from their system. * Cash or continued funding in the case of a non-profit or government agency John R. Broomfield is a Fellow of the Chartered Quality Institute, the VP responsible for management systems consulting with QMI, a certified instructor of lead management system auditors and a certified lead auditor with IRCA (since 1989) and RABQSA.