List of Documented Information (Document & Records)

Similar documents
Sections of the Standard. Evidence / Comments. (Y) / Nonconforming (NC)

Clause Map IATF 16949:2016 to ISO/TS 16949:2009

Awareness Session for Transition to IATF 16949:2016

IATF - International Automotive Task Force IATF 16949:2016 Sanctioned Interpretations

IATF - International Automotive Task Force IATF 16949:2016 Sanctioned Interpretations

Transitioning from ISO/TS 16949:2009 to IATF 16949:2016 Presented by Brandon Kerkstra Revision: 10/24/2016

Comparison ISO/TS (1999) to QS 9000, 3 rd edition (1998)

Supplier Quality System Survey

JDI Quality Assurance Guideline

IATF - International Automotive Task Force IATF 16949:2016 Frequently Asked Question (FAQ)

IATF - International Automotive Task Force IATF 16949:2016 Frequently Asked Question (FAQ)

Vendor Qualification Survey

Correlation Matrix & Change Summary

SUPPLIER SURVEY FORM Instructions

QUALITY MANUAL Rev. 13 Effective date:

SUPPLIER QUALITY MANUAL

QUALITY MANAGEMENT SYSTEM DOCUMENT

QUALITY MANAGEMENT SYSTEM DOCUMENT

ANCHOR ISO9001:2008 RPR-004 MARINE SERVICES REQUIRED PROCEDURE NON-CONFORMING PRODUCTS

ISO 9001: 2000 (December 13, 2000) QUALITY MANAGEMENT SYSTEM DOCUMENTATION OVERVIEW MATRIX

QUALITY MANAGEMENT SYSTEM POLICIES AND PROCEDURES

NATO STANDARD AQAP-2310 NATO QUALITY ASSURANCE REQUIREMENTS FOR AVIATION, SPACE AND DEFENCE SUPPLIERS

Correlation matrices between ISO 9001:2008 and ISO 9001:2015

Supplier Quality Requirements SQR-1.0 Rev. 3

ISO 9001:2015. Quality Management System. Manual

IPD Quality Management System Supplier Questionnaire Instructions

NATO STANDARD AQAP-2110 NATO QUALITY ASSURANCE REQUIREMENTS FOR DESIGN, DEVELOPMENT AND PRODUCTION

Automotive QMS Update IATF 16949:2016 September 2016

Automotive QMS Update IATF 16949:2016. September 2016

IATF - International Automotive Task Force IATF 16949:2016 Frequently Asked Question (FAQ)

Quality Manual QM -07 Approval: D. Wheeler. AARD Spring & Stamping Quality Manual. Quality Manual. Page 1 of 24

IATF 16949:2016 TRANSITION INFORMATION

IATF transition. Only 1 year to go for over 69,000 ISO/TS16949 certified organizations to transition to ISO9001: 2015 and IATF 16949: 2016.

QUALITY SYSTEM MANUAL

ISO9001 QUALITY POLICY MANUAL

QUALITY MANUAL. Number: M-001 Revision: C Page 1 of 18 THIS DOCUMENT IS CONSIDERED UNCONTROLLED UNLESS ISSUED IDENTIFIED AS CONTROLLED

QUALITY MANUAL QM0492 ISO SUPPLEMENT III

Desk Audit of. Based on Federal Transit Administration (FTA) Quality Assurance and Quality Control Guidelines FTA-IT

BAITY SCREW MACHINE PRODUCTS QUALITY MANUAL

CO-ORDINATION OF NOTIFIED BODIES PPE Regulation 2016/425 RECOMMENDATION FOR USE

KEY PERSON MANAGEMENT SYSTEMS CERTIFICATION. (attach copy of certificate) MAIN CUSTOMERS

QMS Qualitäts-Management-Systeme. Key Points Regarding ISO/ TS 16949: 2009 If you have further questions let us know. We are ready to help.

Reference Paragraphs. Appendix B AQS Auditor Handbook

Quality Manual. Specification No.: Q Revision 07 Page 1 of 14

Monroe Engineering is committed to customer satisfaction; we strive for Continuous Improvement in our products and our people.

MERIT Customer Specific Requirements

Revision. Quality Manual. Multilayer Prototypes. Compliant to ISO / AS9100 Rev C

SUPPLIER QUALITY ASSESSMENT

Quality Commitment. Quality Management System Manual

Supplier Quality Requirements

Supplier Quality Survey. 1. Type of Business: g) Commodities supplied? Supplier Changes/comments: 2. Headcount breakdown by group: Purchasing

Control Of Non-conforming Material

Comparison of Requirements ISO/TS vs. AS9100 and ISO 13485

QUALITY ASSURANCE MANUAL

APS Cleaning Quality Management System Scope of Certification The provision of commercial and industrial cleaning services throughout Queensland.

SUPPLIER QUALITY MANUAL

Quality Manual ISO 9001:2008 ISO 9001:2015

AESOP 15604; ISSUE 2; STATUS PENDING APPROVAL; AUTHORITY CARL BLAZIK This document is the property of NSF ISR. Page 1 of 9

25 D.L. Martin Drive Mercersburg, PA (717)

NQA-1 Graded Approach, 55-Gallon Drum Summary

AUTOMOTIVE QMS UPDATE TRANSITIONING TO IATF 16949:2016

SUPPLIER MANUAL Quality Policy

OPERATIONS MANUAL ISO 9001 Quality Management System

Customer specific requirements of DAG September 2017

AS 9100 Rev C Quality Systems Manual AS-050C-QM

NMT Specialized Machining Inc & NMT General Machining Inc AS 9100 Rev C Quality Systems Manual

Supplier Quality Terms & Conditions

TriMark QUALITY POLICY MANUAL

Global Supplier Manual Appendix U FCA EMEA Customer Specific Requirements for Suppliers. October 26, 2017

Moving from ISO/TS 16949:2009 to IATF 16949:2016. Transition Guide

Quality Honeycomb Supplier Quality Requirements

CAPITAL AVIONICS, INC. Quality Manual

PCA ELECTRONICS, INC. Quality Manual

Quality System Manual

14620 Henry Road Houston, Texas PH: FX: WEB: QUALITY MANUAL

Quality management systems

Odyssey Electronics, Inc Fairlane Livonia, MI 48150

QMS Team: MR and all HODs (Internal Auditors) MR March 10. Quality policy Define quality policy The Steering committee Objectives and targets

SAE AS9100 Revision C Requirements beyond ISO 9001:2008 UPDATING YOUR MANAGEMENT SYSTEM

Business Management System Manual Conforms to ISO 9001:2015 Table of Contents

INTERNATIONAL STANDARD

Supplier Audit Procedure /20/17

SUPPLIER QUALITY SYSTEM SURVEY

Customer Specific Requirements. For Use with ISO/TS16949 And ISO 9001

The following is an example systems manual from a low volume (TE, but not an automotive supplier) company.

ANCHOR ISO9001:2008 RPR-006 MARINE SERVICES REQUIRED PROCEDURE PREVENTATIVE ACTION

Stanley Industries, Inc. ISO 9001:2008 Quality Policy Manual

ISO 9001:2015 QUALITY MANAGEMENT SYSTEM POLICIES AND PROCEDURES

Blue Chip Engineered Products Supplier Quality Manual

Quality Systems Manual

QUALITY MANUAL. Origination Date: XXXX. Latest Revision Date. Revision Orig

SUPPLIER QUALITY SYSTEM SURVEY

Eagle Machining, Inc.

TURBO MACH A DIVISION OF VT SAA

Continental Steel & Tube Co. Quality Manual

PRECISE INDUSTRIES INC. Quality Manual

UPGRADE ASSESSMENT CHECKLIST

ISO 9001:2008 Quality Management System QMS Manual

Quality Manual. AARD Spring & Stamping Quality Manual

Document Type: Main Process: Revision Level: Page: POLICY QUALITY ASSURANCE 3 1 of 6 Process Owner Title:

Transcription:

As per IATF 16949:2016 Clause Type Clause Reference 4.3 Determining the scope of the quality management system 5.1.1.1 Corporate responsibility The only permitted exclusion for this Automotive QMS Standard relates to the product design and development requirements within ISO 9001, Section 8.3. The exclusion shall be justified and maintained as documented information The organization shall define and implement corporate responsibility policies, including at a minimum an antibribery policy, an employee code of conduct, and an ethics escalation policy ("whistle-blowing policy"). 5.2 quality policy be available and be maintained as documented information 5.3.1 Organizational roles, Top management shall assign personnel with responsibility and authority to ensure that customer requirements are responsibilities and authorities - met. These assignments shall be documented. supplemental 6.1.2.1 Risk analysis as evidence of the results of risk analysis. 6.1.2.2 Preventive action documented information of action taken & evaluate effectiveness 6.1.2.3 Contingency plans 6.2 Quality objectives and planning to achieve them 7.1.5.1.1 Measurement systems analysis List of ed Information ( & s) document the contingency plans and retain documented information describing any revision(s), including the person(s) who authorized the change(s) The organization shall maintain documented information on the quality objectives. s of customer acceptance of alternative methods shall be retained along with results from alternative measurement systems analysis 7.1.5.2 Measurement traceability the basis used for calibration or verification shall be retained as documented information The organization shall ensure that calibration / verification activities and records 7.1.5.2.1 Calibration / verification records of the calibration and maintenance activities for all gauging (including employee-owned equipment, records customer-owned equipment, or on-site supplier-owned equipment) 7.1.5.3.1 Internal laboratory review of related records 7.1.5.3.2 External laboratory External/commercial/independent laboratory facilities used for inspection, test, or calibration services by the organization shall have defined laboratory scope that includes the capability to perform the required inspection, test, or calibration Compiled By - Arun Kumar Sharma 1 of 5 www.submastery.com

7.1.6 Organizational knowledge The organization shall determine the knowledge necessary for the operation of its processes and to achieve conformity of products and services. This knowledge shall be maintained and be made available to the extent necessary. 7.2 Competence retain appropriate documented information as evidence of competence. 7.2.3 Internal auditor competency Where training is provided to achieve competency,documented information shall be retained to demonstrate the trainer's competency with the above requirements. 7.3.1 Awareness - supplemental The organization shall maintain documented information that demonstrates that all employees are aware of their impact on product quality and the importance of their activities in achieving, maintaining, and improving quality, including customer requirements and the risks involved for the customer with nonconforming product. 7.5.1.1 Quality Manual 7.5.3.2.1 retention 7.5.3.2.2 Engineering specifications document (i.e. matrix) indicating where within the organization's quality management system their customer specific requirements are addressed, process interaction, reference to list of organization process Production part approval documented information may include product, applicable test equipment records, or approved test data. The organization shall retain record of the date on which each change is implemented in production. Implementation shall include updated documents. 8.1 Operation planning and control determining, maintaining and retaining documented information to the extent necessary: 8.2.3.1.1 Review of the requirements for products and services - supplemental 8.2.3.1.2 Customer-designated special characteristics The organization shall retain documented evidence of a customer-authorized waiver 8.2.3.2 No Tittle Product & Service requirements review record 8.2.4 Changes to requirements for products and services 8.3.2 Design and development planning 8.3.2.3 Development of products with embedded software 8.3.3 Design and development inputs The organization shall conform to customer requirements for designation, approval documentation, and control of special characteristics. The organization shall ensure that relevant documented information is amended, and that relevant persons are made aware of the changed requirements, when the requirements for products and services are changed. the documented information needed to demonstrate that design and development requirements have been met. Using prioritization based on risk and potential impact to the customer, the organization shall retain documented information of a software development capability self-assessment. on design and development inputs. Compiled By - Arun Kumar Sharma 2 of 5 www.submastery.com

8.3.3.1 Product input 8.3.3.2 Manufacturing process input 8.3.3.3 Special characteristics 8.3.4 Design and development controls The organization shall identify, document, and review product design input requirements as a result of contract review. The organization shall identify, document, and review manufacturing process design input requirements documentation of all special characteristics in the drawings (as required), risk analysis (such as FMEA), control plans, and standard work/operator instructions documented information of these activities is retained. 8.3.4.4 Product approval process The organization shall obtain documented product approval prior to shipment, if required by the customer. 8.3.5 Design and development outputs 8.3.5.2 Manufacturing process output 8.3.6 Design and development changes 8.3.6.1 Design and development changes - supplemental 8.4 Control of external provided processes, products and services / 8.4.1 General 8.4.2.3.1 Automotive productrelated software or automotive products with embedded software on design and development outputs. The organization shall document the manufacturing process design output in a manner that enables verification against the manufacturing process design inputs. If required by the customer, the organization shall obtain documented approval, or a documented waiver, from the customer prior to production implementation. For products with embedded software, the organization shall document the revision level of software and hardware as part of the change record. for any necessary actions arising from the evaluations. The organization shall require the supplier to retain documented information or a software development capability self-assessment. 8.4.2.4.1 Second-party audits The organization shall retain records of the second-party audit reports. 8.5.1.1 Control plan 8.5.1.2 Standardized work - operator instructions and visual standards The organization shall develop control plans at the system, subsystem, component and/or material level for the relevant manufacturing site and all product supplied, including those for processes producing bulk materials as well as parts. The standardized work documents shall also include rules for operator safety. 8.5.1.3 Verification of job set-ups retain records of process and product approval following set-up and first-off/ last-off part validations. Compiled By - Arun Kumar Sharma 3 of 5 www.submastery.com

8.5.1.5 Total productive documented maintenance objective maintenance 8.5.1.6 Management of production tool design modification documentation, including engineering change level of the product; tool modification and tooling and manufacturing, test, revision to documentation 8.5.2.1 Identification and ensure documented information is retained in the formal (electronic, hardcopy, archive) that enables the traceability- supplemental organization to meet the response time requirements (For Traceability) When the property of a customer or external provider is lost, damaged or otherwise found to be unsuitable for use, 8.5.3 Property belonging to the organization shall report this to the customer or external provider and retain documented information on what customers or external providers has occurred. describing the results of the review of changes, the person(s) 8.5.6 Control of changes authorizing the change, and any necessary actions arising from the review. 8.5.6.1 Control of changes - retain records of verification and validation, retain documented approval, prior to implementation of the change; The organization shall identify, document, and maintain a list of the process controls, including inspection, 8.5.6.1.1 Temporary change of measuring, test, and error-proofing devices, that includes the primary process control and the approved back-up or process controls alternate methods. 8.6 Release of products and services 8.6.2 Layout inspection and functional testing 8.6.4 Verification and acceptance of conformity of externally provided products and services 8.7.1.1 Customer authorization for concession 8.7.1.4 Control of reworked product on the release of products and services. A layout inspection and a functional verification to applicable customer engineering material and performance standards shall be performed for each product as specified in the control plans. Results shall be available for customer review. second-party or third-party assessments or audits of supplier sites when coupled with records of acceptable delivered product conformance to requirements; The organization shall maintain a record of the expiration date or quantity authorized under concession. documented information to verify compliance to original specifications. retain documented information on the disposition of reworked product including quantity, disposition, disposition date, and applicable traceability information. documented information for repair confirmation in accordance with the control plan or other relevant 8.7.1.5 Control of repaired product The organization shall obtain a documented customer authorization for concession for the product to be repaired. on the disposition of repaired product including quantity, disposition, disposition date, and applicable traceability information. Compiled By - Arun Kumar Sharma 4 of 5 www.submastery.com

8.7.1.6 Customer notification 8.7.2 Control of nonconforming outputs 9.1.1.1 Monitoring and measurement of manufacturing processes 9.2 Internal audit Notify the customer(s) in the event that nonconforming product has been shipped. Initial communication shall be followed with detailed documentation of the event. records of actual measurement values and/or test results for variable data Significant process events, such as tool change or machine repair, shall be recorded and retained as documented information, maintain records of effective dates of process changes. The organization shall conduct internal audits at planned intervals to provide information retain documented information as evidence of the implementation of the audit programme and the audit results. 9.3.3 Management review outputs as evidence of the results of management reviews. 9.3.3.1 Management review outputs - supplemental 10.2 Nonconformity and corrective action Top management shall document and implement an action plan when customer performance targets are not met. 10.2.3 Problem solving reviewing and, where necessary, updating the appropriate documented information (e.g., PFMEA, control plan). 10.2.4 Error-proofing shall include the testing of error-proofing devices for failure or simulated failure. s shall be maintained. Compiled By - Arun Kumar Sharma 5 of 5 www.submastery.com