Copy Exact Awareness Training. GT Supplier Change Control



Similar documents
ABSTRACT. The Guidelines Section F is related to the Purchasing requirements of NSQ100 (Chapter 7.4). Summary

GLOBAL AEROSPACE PROCEDURE

EVENT MANAGEMENT FRAMEWORK

Supplier Change Notification Process

Surgi Manufacturing Quality Manual

Revision Date Author Description of change Jun13 Mark Benton Removed Admin. Manager from approval

Supplier Quality Assurance Requirements Manual

SUPPLIER GUIDEBOOK. Rev 1.1

SUPPLIER QUALITY MANAGEMENT SYSTEM QUESTIONNAIRE

Reduce Program Costs Through Parts Management

Technical Manufacturing Corporation (TMC) Quality Manual

QUALITY ASSURANCE MANUAL JPM OF MISSISSIPPI, INC.

A multi-purpose and multi-network compliance management software package

Quality Control of your Products in Dynamics AX2012 With Total Quality Control Management. Page

Purchase Order Clauses and Conditions

Supplier Quality Assurance Requirements Manual

Supplier Quality Requirements and Clauses

Cessna - Interiors Manufacturing Facility (IMF) Supplier Quality System Requirements

GxP Process Management Software. White Paper: Ten Most Common Reasons for FDA 483 Observations and Warning Letter Citations

Analytical Products and Solutions. Complete service and maintenance solutions for your analytical equipment. usa.siemens.com/analyticalproducts

Quality Enhancement Unit Environmental Management System Module 6. Document Control

Only the online system has the current version. Verify hard copy against online system before use. VWI

Cartel Electronics. AS 9100 Quality Systems Manual

Quality Management System Manual

Quality Manual ALABAMA RESEARCH & DEVELOPMENT. This Quality Manual complies with the Requirements of ISO 9001:2008.

KEBA 2014 We reserve the right to make technical modifications. No liability accepted for information provided. All rights reserved.

Documents, Records and Change Control

Bogue Machine Company, Inc. Business Instruction

New Program Quality Requirements for Suppliers (NPQR) For Limited Manufacturing of Components and/or Processes for Engineering Certification

Quality Management System General

GENERAL WELDING & FABRICATING, INC. 991 Maple Road Elma, New York 14059

Eagle Machining, Inc. Quality Management System

Supply Chain Management

Achieve greater efficiency in asset management by managing all your asset types on a single platform.

ORACLE PROCESS MANUFACTURING QUALITY MANAGEMENT

4.0 Receiving Process

Big Data for Manufacturing: 4 use cases for optimizing product offerings, supply chain, and competitive advantage.

ALL PRODUCTS MFG & SUPPLY

National Equipment Management Policy Country

Maintenance in instrumentation Maintenance with concept and technology focusing on results

Contractor Performance Report Scoring Guide

Quality Management Systems Manual

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

New Program Quality Requirements for Suppliers (NPQR) For Limited Manufacturing of Components and/or Processes for Engineering Certification

Big Data for Manufacturing

CCD MARINE LTD QUALITY MANUAL PROCEDURE Q Date: Title. Revision: QUALITY MANUAL PROCEDURE Q September 2014

The Fulfillment of AS 9100 Rev C Requirements by EnterpriseIQ

Turbo Resources International Quality Procedure

Pacific Gas and Electric Company

BASE CONSTRUCTION INC

De-Risking the Supply Chain: Cisco s Risk Intelligence and Analytic Tools

Welcome! Frank Teleso. Quality Manager

Supply Chain Optimization

SQM-H. This Handbook is a summary of the processes and documents of the supplier quality management 1/13

INTRODUCTION: PURPOSE:

Standard Practice for Quality Control Systems for Nondestructive Testing Agencies 1

Maximizing Equipment Uptime

QUALITY MANAGEMENT SYSTEM REQUIREMENTS General Requirements. Documentation Requirements. General. Quality Manual. Control of Documents

Supplier Relationship Management. Supplier/Vendor Relationship and Compliance Management

AS9100 Quality Manual

QUALITY OPERATING PROCEDURE QOP QUALITY ASSURANCE SYSTEM MANUAL

Quality Management Training Agenda for

Quality Management Plan Procedure

Quality Assurance QUALITY ASSURANCE PLAN

ERP s Automated Workflows Deploy Advanced Business Processes

Table of Contents 1. SCOPE APPLICABLE DOCUMENTS TERMS AND DEFINITIONS QUALITY MANAGEMENT SYSTEM...4-8

Quality Management System Manual

Unexpected Changes. Reliable Results.

Gulfstream Production Certificate Operations

THE ESSENTIAL GUIDE TO IMPLEMENTING VENDOR PERFORMANCE METRICS in your Import Supply Chain

Product Order Quality Requirements Meggitt (Orange County), Inc.

Software License Monitoring

Warranty Agreement. the following agreement is concluded relating to the reimbursement of warranty costs:

The impact of the personal data security breach notification law

Internal Quality Management System Audit Checklist (ISO9001:2015) Q# ISO 9001:2015 Clause Audit Question Audit Evidence 4 Context of the Organization

Quality Management System

AVNET Logistics & EM Americas. Quality Manual

Achieve greater efficiency in asset management by managing all your asset types on a single platform.

Software Asset Management Toolkit

Valuable Metrics for Successful Supplier Management

ORACLE QUALITY ORACLE DATA SHEET KEY FEATURES

ISO 9001:2008 Audit Checklist

SOLUTION BRIEF: CA IT ASSET MANAGER. How can I reduce IT asset costs to address my organization s budget pressures?

GARDNER AEROSPACE SUPPLIER QUALITY REQUIREMENTS MANUAL

Supplier Quality Assurance

Manage your stock effectively

QUALITY MANAGEMENT SYSTEM Corporate

Imperative. Tim Mohn Industry Principal Sparta Systems

SUPPLY CHAIN SERVICES

Seradex White Paper. Engineering Change Process. A Discussion of Issues in the Manufacturing OrderStream

ISO 9001:2000 Gap Analysis Checklist

Field Service in the Cloud: Solving the 5 Biggest Challenges of Field Service Delivery

AEROSPACE STANDARD. Quality Management Systems - Requirements for Aviation, Space and Defense Organizations RATIONALE

ISO 9001 Quality Systems Manual

RTP s NUCLEAR QUALITY ASSURANCE PROGRAM

2012 STC. All Rights Reserved. The reproduction, duplication or distribution of this document is prohibited without express permission of STC.

Sargent Controls & Aerospace 5675 West Burlingame Rd. Tucson AZ PHONE: (520) FAX: (520)

Supplier Performance Management Guide. A Technology Leader

Karas Engineering AS9100 QUALITY MANAGEMENT SYSTEM MANUAL

School of Management and Languages Capacity Planning

Transcription:

Copy Exact Awareness Training GT Supplier Change Control

Copy Exact Philosophy What is Copy Exact? What are the Benefits? Expectations & Responsibility What is a Qualified Process? Prevention of Violations Copy Exact Training Outline Change Communication & Management Supplier Change Notification Form & Process Evidence of Training Compliance 2

What is Copy Exact? History Pioneered by Intel Corporation, the original purpose of the Copy Exact methodology was for semiconductor manufacturers to be able to ramp up production quickly and with identical results. Everything which might affect the process, or how it is run is to be copied down to the finest detail, unless it is either physically impossible to do so, or there is an overwhelming competitive benefit to introducing a change. 3

What is Copy Exact? History Copy Exact is a disciplined approach for Design & Process change management throughout the supply chain and it ensures true interchangeability of components & spare parts. Physical Interchangeability (Form & Fit) Equivalent parts capable of being installed, removed, or replaced without sustaining or causing damage, misalignment, or interference. Functional Interchangeability Parts equivalent in safety, characteristics of operation, performance, durability, serviceability, structural strength, material, & protective finish. 4

What are the Benefits? Copy Exact enables the delivery of product from multiple production facilities, supporting Intel s Virtual Factory concept. Faster production ramp up that improves product availability. Improves consistency in quality performance between different customer fabrication facilities. Reduces time & money invested in re-engineering what should be the same process. 5

Expectations & Responsibility No changes to Design, Process, Equipment, or Materials without prior notification & approval. Once a process is approved through acceptance of the First Article it is then considered Locked In. This is also known as a Process of Record (POR) or Process Qualification Program (PQP). This applies to all parts whether or not a formal POR or PQP exists. The prime supplier is responsible for ensuring all sub-tier suppliers & processors are working to the same Copy Exact requirements. 6

Expectations & Responsibility In the case a change must be made: Any change is to be implemented with control & the suitable amount of transition time (minimum of 9 months). Any change is to be justified with adequate benefits. The change needs to be validated with appropriate test data. Quality is the responsibility of Everyone! 7

What is a Qualified Process? All process steps are identified with controls in-place to ensure repeatability. Critical features have been identified with a documented measurement method & inspection frequency established. Production data is collected & monitored, the appropriate response and escalation steps are identified in the event data begins to trend outside of control limits. 8

What is a Qualified Process? All calibration & maintenance requirements involved in the production, inspection, & testing are documented & complied with. First Article is completed to ensure part meets intent and upon approval locks in the Process. 9

Prevention of Violations What is a Copy Exact Violation? When a supplier or sub-tier supplier makes an unauthorized, uncontrolled, and/or undocumented deviation to the established system configuration or to the system component manufacturing procedures without notification or adequate prior warning. A violation may be discovered during a failure analysis or through audit even if no impact was detected. 10

Prevention of Violations What is the Result of a Copy Exact Violation? An unintended result could potentially effect: Safety & Ergonomics Process Controls Tool Reliability Manufacturing Control & Automation Obsolescence of Downstream Operations & Procedures. Obsolescence of Spare Parts Inventory Require New Tool Shipments & Qualification 11

What is the Cost of a Violation? Prevention of Violations Seemingly insignificant changes in a component may have a serious adverse effect in the semiconductor manufacturing process with money lost in materials and equipment down time. Violations discovered by our customers through audit or investigation may result in Greene, Tweed & Co s supplier approval rating lowered, business and financial penalties. Loss of business for GTC and it s supply base! 12

Prevention of Violations Do not make any changes unless approved by Greene, Tweed & Co. & notify us when there is a plan to: Change in manufacturing location. Change to a material or special process supplier. Revision or part number change. Be proactive on obsolete material & communicate changes. Plan for last time buys to bridge time required for requalification. 13

Prevention of Violations Make Copy Exact awareness part of your business culture. Educate your own supply chain on Copy Exact requirements. Communicate up front with Greene, Tweed & Co. s Supply Chain Specialists and use them as a resource in planning changes. 14

Supplier Change Notification Process Request the current revision Supplier Change Notification form from a Greene, Tweed, Co. supply chain specialist. Return the completed form to GTC supply chain specialist including: Description of the change. Justification for the change. Part numbers affected. On-hand balance of parts manufactured to the current qualified process. Is a last time buy possible to the current qualified process & what would be the maximum quantity available for this. If applicable, identification of proposed replacement material. 15

Supplier Change Notification Process The Greene, Tweed & Co. will forward the request to the appropriate internal engineering and customer service functions for review and disposition. If approval is granted, then the GTC supply chain will immediately contact the supplier to confirm the controlled plan for implementation and requalification. 16

Evidence of Training Compliance All suppliers involved in the Semiconductor business sector of Greene, Tweed & Co. must complete this training & the accompanying Copy Exact test with their employees and their sub-tier suppliers. Copy Exact training should be part of any new hire orientation. The suppliers must send a copy of the training records with test scores to their GTC Supply Chain Specialist as evidence of compliance. The training record must include signatures from the supplier s Quality & Operations management. 17