ITT Motion Technologies Supplier Quality Manual

Size: px
Start display at page:

Download "ITT Motion Technologies Supplier Quality Manual"

Transcription

1

2 ITT Motion Technologies Supplier Quality Manual PO rev. 11 Oct. 2010

3 I am pleased and proud to introduce first time ever our Supplier Quality Manual, key tool for future development of ITT Motion Technologies. Since we are looking for fastest growing and to achieve all future challenges, our supplier base will be crucial instrument for it and based on that we'll spend as much as we need in order to develop our relationship and partnership with our suppliers in the same way we do with our customers. Full compliance of SQM will be key selection ingredient for our current and future suppliers. Looking forward to winning together. President ITT Motion Technologies, S.Torrisi ITT Motion Technologies develops and produces competitive components and systems looking for faultless quality in cooperation with its Suppliers, who bring their own know-how and capacity to innovate. ITT has on innovation, quality and competitiveness his company footprint: all the process to improve this areas must be pursued tirelessly. These depends heavily on our supplier capacity for it: Supplier commitment is then a necessary condition for our progress. To maintain leadership role, side to innovative and faultless products implementation, quality of purchases is considered one of the key driver for it, to eliminate waste and perturbations. The target of this strong integration with our supplier base is to: achieve continuous innovation in term of products and manufacturing process to maintain market leadership, supporting ITT production preventing any disturbances through high level of supplies quality and service level, developing effective productivity plans. To identify the best partners, ITT Motion Technologies is looking to his supplier base through a detailed evaluation of each company strength on the areas of quality, innovation, service and cost. The scope of the Supplier Quality Manual, as deployment of ITT Supplier Expectations (SEITT), is to provide clear expectations of ITT and is the basis for integration between ITT and its Suppliers towards achieving all objectives. ITT Motion Technologies clearly recognize the importance of Suppliers contribution on this path and how quality of items delivered to ITT are decisive factor in ensuring the correct form, fit, function and reliability of ITT products, the competitive flow of these products and services through ITT factories. For all of these reasons ITT trust on Your full commitment. ITT Motion Technologies Global Quality Director, P. L. Scarabelli ITT Motion Technologies Global Purchasing Director, M. Pesci 1

4

5 Summary I - SQAE Supplier Quality Aptitude Evaluation 1. GOALS 2. SUPPLIER CATEGORIES 3. PRE-EVALUATION PROCESS 4. FOLLOW UP AUDIT 5. AUDIT FREQUENCY II - PQA Product Quality Assurance 1. OBJECTIVES 2. PQA PROCEDURE Scope of application PQA Procedure - Stage 1: Selection of suppliers, product and references - Stage 2: Definition of ITT Motion Technologies requirement file with the supplier - Stage 3: Definition and Acceptance of the PQA Dossier - Stage 4: Validation of production process (Run@Rate / Process audit) - Stage 5: acceptance of initial samples - Stage 6: Probationary Period - Stage 7: PQA Management III - CQI Continuous Quality Improvement 1. GOALS 2. CLAIM PROCESSING Definition of Claims Claim Processing CSL: Control Shipping 3. QUALITY, COST AND LOGISTICS PERFORMANCE MEASUREMENT Definition of PPM, %PQA and Service Rate indicators Product Quality Indicator = Q Cost Indicator = C Logistic Indicator = D QCD Indicator 4. VENDOR RATING Score Card pag. 5 pag. 6 pag. 7 pag. 8 pag. 8 pag. 9 pag. 10 pag. 10 pag. 11 pag. 11 pag. 11 pag. 11 pag. 12 pag. 12 pag. 13 pag. 13 pag. 15 pag. 16 pag. 16 pag. 17 pag. 18 pag. 19 pag. 19 pag. 20 pag. 21 pag. 21 pag. 22 pag. 23 pag. 23 3

6

7 I - SQAE Supplier Quality Aptitude Evaluation 1. Goals An efficient Quality System is fundamental to produce parts with high quality level. It must: guarantee the reliability of tasks performed and the information communicated (in particular to Customer/Supplier interfaces); drive continuous improvement; ensure the continuity of the company s know-how. It is based on: a clearly defined and expressed Quality Policy; an organization capable of assuring quality and process ownership at all stages of the product s life with ITT Motion Technologies project development phases; consistent ownership of each process step; the commitment to work with ITT Motion Technologies in a spirit of partnership and progress. 5

8 2. Supplier categories ITT Motion Technologies classifies its supplier in three categories of supplier sites: CATEGORY OF SUPPLIER DESIGNER MANUFACTURER SUB-CONTRACTOR SUPPLIER RESPONSIBILITIES Responsible for the design and supply of a function defined by ITT Motion Technologies. The integrated supplier-designer participates in the development and definition of the function with ITT Motion Technologies Responsible for the development of a manufacturing process and the manufacturing of a product designed by ITT Motion Technologies Responsible for the manufacturing of products designed by ITT Motion Technologies using manufacturing processes developed by ITT Motion Technologies Supplier-designers Supplier-Designer Aptitude Evaluation - SDAE will be performed by the ITT Motion Technologies R&D Department and Purchasing Department with the participation of the Supplier Quality to determine the supplier s aptitude as a designer. Manufacturers Supplier of this category provides: specific components on ITT Motion Technologies requirements that includes key/safety aspects; generic components on ITT Motion Technologies requirements w/o key aspects; standard components (by catalogue, on the shelf parts); raw materials. Except suppliers of standard components, Supplier Evaluation Matrix - SEM activity will be performed by ITT Motion Technologies. Sub-Contractor Supplier of this category provides: specific components on ITT Motion Technologies requirements that includes key/safety aspects; generic components on ITT Motion Technologies requirements w/o key aspects. Supplier Evaluation Matrix - SEM will be performed by the ITT Motion Technologies R&D Department and Purchasing Department. 6

9 3. Pre-evaluation process SUPPLIER PRE-EVALUATION SQAE is the ITT Motion Technologies evaluation process for potential suppliers site, or for sites already included in the supplier list. All of ITT Motion Technologies potential suppliers must achieve a positive evaluation considering the panel of suppliers in the same business field. The criteria for comparison are collected on the Supplier Evaluation Matrix - SEM on follows chapters: STRATEGY AND MANAGEMENT, GENERAL SUPPLIER KEY FACTS (FINANCIAL, MARKET POSITION, ETC), R&D (FOR DESIGNER SUPPLIERS), PRODUCTION, QUALITY, LOGISTICS, COMPETITIVENESS. On contrary, existing supplier sites may be considered for exit strategy from the panel if they do not meet proper level of evaluation rating. For potential supplier it requires as background: pre-audit PCPA process on existing products/processes same or similar to ones to be purchased by ITT Motion Technologies; review of potential supplier quality certification and self-assessment report; review of supplier key main facts data (financial, market position, etc); a design audit for designer suppliers. The pre-selection process could classify the supplier in 4 possible levels: RATING SCORE & QUALITY CERTIFICATES RESULTS & COSTRAINTS OUTCOME A SEM > 90 and ISO/TS CE CE Fully Compliant Drive continuous improvement Supplier site is eligible for a new application development and for the production of new or transferred products AB 80 < SEM < 90 and ISO 9001 CE Mostly compliant Need Improvement Supplier site is eligible for new application development and for the production of new or transferred products with introduction of an improvement plan B 70 < SEM < 80 or No QMS Certification Not fully compliant Need Development ITT can sign a first contract with the supplier. The supplier must obtain upgraded status in 6 month max. C SEM<70 and No QMS Certification Not compliant New Business Hold The supplier must provide an action plan to solve major non conformities The supplier has 6 month to obtain a score > 80, to undertake an Automotive certification process and to have a qualified process. 7

10 4. Follow-up audit The aim of the follow-up audit evaluation procedure is to check the progress of the corrective action plans implemented following the initial audit. A follow-up audit must be performed: no later than 6 months after the evaluation audit for sites with a rating of B/AB; if the follow-up audit confirms that corrective actions have been implemented to resolve all critical problems, the supplier can be upgraded; if necessary, a second follow-up audit can be performed no later then twelve months after the evaluation audit. In this case supplier might be requested to cover relevant expenses, or activity done by 3 rd party at his charge. 5. Audit frequency Supplier sites will be re-evaluated at least once every two years and at least once every three years for quality certification. A new audit will be scheduled if there have been major organizational changes at the supplier site or if there have been serious or repeated incidents which can be shown to have resulted from a failure in the quality system ITT Motion Technologies recommends that all its Suppliers achieve ISO/TS certification. 8

11 II - PQA Product Quality Assurance 1. Objectives Product Quality Assurance is designed to assure long-term product quality. It results in fewer incoming inspections at ITT Motion Technologies Plants without in any way reducing supplier responsibility for product quality. ITT Motion Technologies objective is to obtain 100% PQA deliveries 9

12 2. PQA procedure PQA The Product Quality Assurance procedure starts with the drawing up of a quality assurance plan for the product/process (APQP File) the aim of which is to provide ITT Motion Technologies with all the guarantees concerning the means to achieve product quality. The APQP File consists of a: ITT Motion Technologies requirements file, quality assurance file, supply chain requirements file, initial samples file, quality monitoring file. SCOPE OF APPLICATION A technology family is a set of products used to achieve the same function, manufactured for ITT Motion Technologies by same supplier site, which rigorously follows the same flow using specific tooling, as the case may be. Standard parts are not considered to be part of PQA procedure. PQA apply also to development samples/prototypes in the terms of certification of: Fit to the development scope of key characteristic (dimensions, materials, treatments, physical characteristics, etc.) Level of representativeness with respect of forecasted final production configuration - materials; - process flow and steps; - jigs/tools and equipment set-up; - production site. 10

13 PQA Procedure The Product Quality Assurance procedure has 7 stages. These stages apply to all customer application project parts and to parts already used in production. STAGE 1: SELECTION OF SUPPLIERS, PRODUCT AND REFERENCES Potential suppliers from approved panel are given a set of functional specifications (supplier-designers) or technical specifications (supplier-manufacturers). At this state, requirements concerning: product specifications, timing milestones, quality and logistics, are defined or restated. Requirements must be updated for components existing or that are carried over to another project. STAGE 2: DEFINITION OF ITT MOTION TECHNOLOGIES REQUIREMENT FILE WITH THE SUPPLIER This file details ITT Motion Technologies requirements concerning the above items together with the documents to be provided by the supplier and / or ITT Motion Technologies during the PQA process. These requirements are drawn up and discussed by ITT Motion Technologies and the supplier during stage 2. At the end of this stage, ITT Motion Technologies finalises the requirement file and sends it to the Supplier for confirmation. STAGE 3: DEFINITION AND ACCEPTANCE OF THE PQA DOSSIER This file formalises supplier responses to ITT Motion Technologies Quality Requirements in term of feasibility, capability of processes, final capacity and timing milestones. It is presented by the supplier and jointly examined with ITT Motion Technologies. Once this file has been examined and approved with regard to the ITT Motion Technologies requirement file, the supplier undertakes to comply with it and submit all proposals for modifying or improving the product or process for approval to ITT Motion Technologies including in the event of a transfer of production. This stage ends with the supplier feasibility confirmation and launch of the tooling production at the supplier. 11

14 STAGE 4: VALIDATION OF PRODUCTION PROCESS / PROCESS AUDIT) The aim of this validation phase is to ensure that the processes and quality procedures drawn up are suitable and efficient for the production lifetime of the product. This stage includes: Verification, if required, of the PQA Dossier; Process Control Plan Audit during The audit is valid only if the process audited is the one that will be used in volume production (equipment and conditions). Following the full production day run, the following reports must be issued: day report: conditions, quantities produced and rejected, analysis of defects, speed of the production line, etc.; PCPA audit report; test report, if the supplier is a designer and if specified in the ITT Motion Technologies requirement file; part inspection report; capabilities (according to PQA dossier requirement files). The process is audited by ITT Motion Technologies by PCPA approach: in case of items not compliant, the supplier must draw up an action plan ad a follow-up audit performed. PCPA audit results are part of PPAP dossier. Initial samples must be taken during the Run@Rate and delivered in volume production packaging together with full documentation as specified in the ITT Motion Technologies Requirement files. Periodic audits of the process must be performed by the supplier at the intervals defined in the control plan. Audit reports and corrective action plans must be available for consultation by ITT Motion Technologies at all times. ITT Motion Technologies will perform process audits at least once every 3 years and reserves the right to carry out new audits whenever sees it fits. STAGE 5: ACCEPTANCE OF INITIAL SAMPLES The aim of Supplier Initial Samples (PPAP) is to check that the product (performance, characteristics, reliability, capability, tests, etc.), production processes, lines and equipment comply with specifications. ITT Motion Technologies uses the PPAP to qualify products on the basis of the validation plan. 12

15 Acceptance of Supplier PPAP by ITT Motion Technologies can only be given if this internal qualification stage is satisfactory. If supplier PPAP is rejected, full production cannot go ahead STAGE 6: PROBATIONARY PERIOD This stage is compulsory for all PQA specific components that includes key/safety aspects and for all non PQA parts. It is designed to optimize and validate quality inspection conditions, once the PPAP have been accepted. Deliveries are subjected to quality inspection for a defined probationary period: during this period supplier is requested to provide with each batch conformity certificate by statistical sampling. The probationary period lasts for at least 2 months and involves at least 7 production batches* of the parts involved. ITT Motion Technologies checks that the product manufactured in line with the APQP Dossier does not present any non-conformance, whatever the cause, during this period. If an incident occurs, the part will be subjected to a new probationary period after an appropriate action plan approved by ITT Motion Technologies, has been effectively implemented. At the end of stage 6, the probationary period inspection reports become part of the APQP Dossier. STAGE 7: PQA MANAGEMENT Stage 7 applies to PQA-ble parts only. PQA STATUS A PQA part is a part that is free pass to ITT Motion Technologies production line: no incoming inspection considered except for product quality audits which are carried out perio- * Batches sizes will be defined with the supplier during preparation of the APQP Dossier. 13

16 dically as defined by ITT Motion Technologies. Free pass parts conformance is guaranteed by the supplier through the strict application of the APQP Dossier. PPAP will be re-qualified in line with the periodicity specified in the ITT Motion Technologies APQP Dossier. PQA status can be maintained if: supplier is approved based achieved rating; no incidents involving the part in question must have occurred during the probationary period and the quality objectives (line ppm) have been achieved. If a part belongs to a technology family, non-conformance can be considered if have been identified in the common production process during the probationary period. If all the above conditions have been met ITT Purchasing Department officially confirms to the supplier the date on which PQA deliveries can start for the part. All PQA deliveries must be identified by a PQA label on all boxes, containers, etc. The supplier must be in a position to inform ITT Motion Technologies on specific request about the results of inspections carried out for each batch delivered in line with the requirements of the APQP Dossier. FINAL ACCEPTANCE OF PQA STATUS Once all requirement has been satisfied the Supplier is requested to sign a final contract indicating the PQA part number list. SUSPENSION OF PQA Any incident will result in the immediate suspension of PQA deliveries. After analysis of the causes, suspension of PQA is confirmed for: the technology family of part, if it is the generic process that is at fault; the part involved if a specific process is found to be at fault. In all cases, ITT Motion Technologies will give the supplier written notification of the date for resumption of PQA deliveries after the problem has been solved and a new probationary period completed. If a product or process is modified or production transferred, PQA deliveries are suspended. It may be decided by ITT Motion Technologies Purchasing Quality that the supplier must go through stages 2 to 6 again. NOT ACHIEVEMENT OF PQA Parts that do not achieve PQA status has to be checked 100% with respect to key characteristics; checking certificates has to be attached to shipping documentation identified as parts 100% certified. For parts/material that are involved on ITT Motion Technologies processes related to legal/safety requirements, supplier might be requested to submit for every batch specific certificates showing single measured values. Missing documentation/incorrect identification will be raised as a claim and relevant cost charged at supplier. 14

17 III - CQI Continuous Quality Improvement 1. Goals ITT Motion Technologies goals in terms of Supplier s Product Quality and Logistics performance, can be managed with Single Supplier Progress Plans. These Progress Plans are designed to help ITT Motion Technologies and its Suppliers to continuously improve product quality competitiveness and the Supply Chain performances. In this way ITT Motion Technologies can integrate these improvements into its own products as customer logistics and quality support. The development of new business between ITT Motion Technologies and its suppliers is strongly related on the achievement of the performance levels defined in Cost, Quality and Logistics Progress Plans, based on the metrics shown in this chapter. In these sense the metrics are considered to drive ITT Motion Technologies strategic business approach on supplier base definition. 15

18 2. Claim Processing DEFINITION OF CLAIMS CATEGORY SIGNIFICATION EXAMPLE The problem affects ITT Motion Technologies internal or external customer. The problem disrupts production at ITT Motion Technologies. The problem is identified on delivery to ITT Motion Technologies and does not disrupt production. ITT Motion Technologies Customer line or end of line reject. ITT Motion Technologies end-of-line rejects. Sorting, rework and production line disruption. Repeated non-conformance identified in the manufacturing process. Non-conformance identified at Incoming Inspection. METHOD OF CALCULATION: Category 1 (C1) Any customer complaint the cause of which is the non-conformance of a primary component, or what ever related to safety characteristic is recorded as a C1 claim. Category 2 (C2) A C2 claim is recorded when a complaint is made due to disruption to ITT Motion Technologies lines. Category 3 All non-conformance identified using the sampling method, whether due to the product itself or delivery conditions, is recorded as a claim. Definition of a recurrent claim A claim which occurred on the same reference, having the same effect and out of different batches. Costs generated In addition to direct and indirect costs generated by the claims, a debit note can be issued including administrative fixed costs as indicated on General Terms and Conditions. Moreover to these costs, ITT Motion Technologies reserves its right to apply additional penalties depending on severity or reoccurrence of the generated claims. 16

19 CLAIM PROCESSING When a defective product is identified, ITT Motion Technologies will notify the supplier of the claim describing the issue identified. Supplier is requested to activate internal problem solving analysis, focusing on root cause definition (Ishikawa, 5 why s tools...) and validation on both technical and control areas, following 8D approach. Structural solution implementation is requested to ensure effective and stable process improvement. Supplier has to ensure proper information flow and prompt feedback, by clear resources appointment for resolution ITT need. Within 24 hours of the notification (Quick Response) the supplier undertakes to: Identify and remove all defective products or products that are likely to have the same defect from all stocks of finished products and WIP. Send a team of competent people to carry out sorting and inspection operations and recover products from ITT Motion Technologies, if ITT Motion Technologies so requests. If this is not possible directly from the supplier side, can be activated at supplier charge external sorting providers from an approved panel. Come to ITT Motion Technologies site if ITT Motion Technologies so requests, to analyze the problem, even if it is uncertain at this stage of analysis that the supplier is responsible for the defect. Replace the defective batch(es) of products within 24 hours of notification of the claim by ITT Motion Technologies and label those batches as products that are not defective. Within five days of the notification date the supplier undertakes to: Perform an exhaustive analysis of the root causes of the non-conformance, both on technical and on control field, using the ITT 8D method. Root cause validation results has to be highlighted. Issue ITT Motion Technologies with a corrective and preventive action plan to be approved by ITT Motion Technologies Supplier Quality. Within ten days of the notification date the supplier undertakes to: Implement the short term actions presented above and obtain validation of results from ITT Motion Technologies Supplier Quality. Extend the implementation of these actions to all production for ITT Motion Technologies. ITT Motion Technologies Production lines Disruption If a defective part is found during production operations (Category 2) ITT Motion Technologies will request immediately for the Supplier to sort affected parts with its own personnel if possible or by activating an external provider. The sorting may be requested also on already ITT produced parts instead of the single components where this is needed due to ITT production constraints. 17

20 If needed, reworking operations of both component and finished goods will be agreed. In no case the Supplier is allowed to rework ITT Motion Technologies products. All direct cost will be invoiced to the Supplier, if they are at fault, while awaiting a return to the required quality level. The supplier will also be invoiced for all extra costs generated by the claim, including the ones generated by sorting of effected parts/goods back from Customer in case of Category 1 claim occurs. CSL1 AND 2 (CONTROLLED SHIPMENT LEVEL 1 AND 2) In case of recurrent non-conformance or heavy impact on product/production at Customer/ITT side, where the supplier clearly does not have sufficient production process control, the CSL procedure will be applied. CSL1 and CSL2 are provisional procedures implemented with a view to guarantee certified deliveries while awaiting the re-establishment of the conformance of the production process. CSL1 Following a request from ITT Motion Technologies, the Supplier will implement sorting of their production in accordance with criteria defined by ITT Motion Technologies Supplier Quality. The Supplier formally guarantees the conformance of goods delivered for each delivery that takes place while CSL1 is in the process of implementation, informing SQ sending results summary report. Audit about proper CSL implementation has to be performed at the beginning of the activity (supplier or ITT SQ). When the supplier fails to meet the commitments stipulated by CSL1, CSL2 status is recommended. CSL2 Requires that an external company validated by ITT Motion Technologies implements sorting in line with criteria defined for CSL1. The cost of sorting will be met by the supplier. Sorting results will be communicated by the external company both to ITT Motion Technologies and supplier. Termination of claims The unique format accepted by ITT Motion Technologies is 8D form, based on ITT problem solving tool. C1/C2 claims will be terminated over the 8D validation, by a process audit of the defective production stage which caused the claim. C3 claims will be terminated by the validation of the corrective action plan described in the 8D Report. With a view to achieving zero defects, the supplier commits to the following: zero recurrent claims; strict application of the PS methodology; the implementation of a formal program for Continuous Improvement. 18

21 3. Quality, Cost and Logistics performance measurement Quality, cost and logistics performance is measured and communicated monthly to suppliers. If objectives are not met, suppliers must communicate an action plan to ITT Motion Technologies to show how they intend to meet them in the future. The objectives that are part of the measurement of supplier performance are defined in conjunction with ITT Motion Technologies and officially communicated. These objectives are reviewed at least an annual basis. ITT Motion Technologies Sites will undertake monthly monitoring of PPMs and the rate of PQA parts so as to facilitate the definition of accurate QCD objectives clustered by commodity. Performances key indicator will be visible on ITT Motion Technologies Procurement portal. DEFINITION OF PPM, %PQA AND SERVICE RATE INDICATORS PPM Indicator The PPM indicator measures the ratio of defective supplier production parts detected wherever (Quality Inspection, in Production and at the Customer) vs relevant incoming quantities. It includes technical defects as well as packaging and labelling errors. ITT Motion Technologies divide PPM in two categories, Gross PPM and Net PPM: the Gross PPM is an indicator of the volume of parts rejected and for which ITT Motion Technologies had disruption (total quantity of claim); the Net PPM is an indicator of the effective number of defectives parts on which were detected the non-conformity after sorting (by ITT Motion Technologies or supplier representative). - NUMBER OF NON-CONFORMING PARTS* GROSS PPM = X ** TOTAL NR. OF PARTS RECEIVED Net Relevant PPM = Number of non-conforming parts detected in the effected batches evaluated as previously mentioned Non conformance is determined in terms of specifications: identification, size, aspect, function, mix, error in quantities, etc. * Only parts that have entered the site; consignment stocks awaiting reception and supplier stocks are not included. ** For raw materials, replace number of parts by number of units, i.e. unit of weight in most cases. 19

22 Non conforming parts formally accepted in deviation by ITT Motion Technologies are not included in the measurement of defective parts; Batches of products that have been destroyed or returned will be recorded as non conforming. In the event that sorting operations have to be carried out at ITT Motion Technologies to which the supplier has agreed and paid for, only the defective parts will be recorded as non conforming. If no reliable sorting have been performed, the whole batch is recorded as being defective. PQA Indicator It includes all APQP process positive at the first time at SOP NUMBER OF ITEMS DELIVERED UNDER PQA (OVER LAST MONTH) % PQA = X 100 NUMBER OF PQABLE ITEMS (OVER LAST MONTH) Service rate A customer order is filled if the quantity delivered is the same as that ordered (or as modified by an acceptance coefficient) and if delivery occurs within a specific time period as defined in the logistics agreement between ITT Motion Technologies and its supplier (month, week, day). SR = CUSTOMER ORDERS FILLED (FOR A GIVEN PERIOD) CUSTOMER ORDERS PRODUCT QUALITY INDICATOR = Q This indicator takes into account the number of C1+C2 claims over the last three months (rolling 3 month) as well as the number of CSL1/2 open in the current month. The result is compared with the result for the previous month and a red, yellow, or green colour code is applied: GREEN YELLOW RED zero claims in absolute value reduction of the number of claims in the current month & no C1 claim or CSL2 no progress or an increase in the number of claims in the current month, C1 claim or CSL2 open in the last month 20

23 Quality Indicator Example INDICATOR MONTH M-1 MONTH M Claims C3M (C1+C2) 25* 17* YELLOW CSL open 1 0 *: (No C1) COST INDICATOR = C This indicator measures economics performance in the current month with a view to evaluate compliance with a progressive reduction required to achieve an end-of-year target. On the basis of comparison with the theoretical curve a Red, Yellow, or Green colour code will be deemed to apply. GREEN YELLOW RED the supplier is under the theoretical curve the supplier indicator is above the theoretical curve not progress or a result that deteriorates in relation to the previous month s performance and the theoretical curve Cost indicator example: INDICATOR MONTH M-1 MONTH M Supplier indicator GREEN LOGISTIC INDICATOR = D This indicator measures the real rate of service for the current month and compares it with the rate of service for the previous month. Red, Yellow, or Green colour codes indicate improved or deteriorating performance GREEN YELLOW RED 100% Service Rate on target an improvement on the previous month s performance no progress or a result that deteriorates in relation to the previous month s performance Logistic indicator example: INDICATOR MONTH M-1 MONTH M Service rate 88% 85% Red 21

24 QCD INDICATOR QUALITY PPM 125 CLAIM C1+C2 2 vs target PQA 90% CSL 1 ECONOMICS SUPPLIER INDICATOR 98,5% DELIVERY SERVICE RATE 87% COMMENTS /ACTION PLAN 22

25 4. Vendor rating SCORE CARD On yearly base will be defined cost, quality and logistics targets that set out implementation plan in terms of results and resources agreed to by ITT Motion Technologies and the supplier. They must be regularly reviewed in line with defined milestones and results compared with objectives. ITT Motion Technologies Vendor Rating Score Card will be based both on SEM status and on QCD performance indicators, and brings to an overall ITT Motion Technologies rating: grow (green) rating will mean ITT Motion Technologies intention to improve business relation; maintain (yellow) rating will indicate the need to keep focus on the supply condition in order to identify an grow/exit approach strategy; exit (red) rating will show New Business Hold and/or exit strategy due to low confidence on supplier capability to achieve ITT Motion Technologies needs. ITT SUPPLIER VENDOR RATING QCD INDICATOR SEM RATING FINDINGS FINAL SCORE: 80/100 RATING AB Vendor rating is discussed between ITT Motion Technologies and suppliers at least on yearly base: specific action plan has to be defined for supplier that has yellow/red ratings. ITT team bases on Vendor Rating the definition of the purchasing strategy that identifies which supplier to grow business with, which to maintain and the ones that, not being compliant with ITT expectation, will be put on business hold or on exit strategy. 23

26 For any other need or explanation, please refer to following reference contact: 24

27

28

GLB QM 02. Supplier Quality Manual 03. 7/11/12 Supplier Quality 1 of 18. Revision Level. Issue Date Issuing Department Page

GLB QM 02. Supplier Quality Manual 03. 7/11/12 Supplier Quality 1 of 18. Revision Level. Issue Date Issuing Department Page 7/11/12 Supplier Quality 1 of 18 7/11/12 Supplier Quality 2 of 18 Table of Contents 1.0 Introduction 3 2.0 Manual 4 2.1 Application 4 2.2 Quality Management System of the Supplier 4 2.3 Quality Management

More information

GE Power Electronics Business Total Quality Management for Suppliers

GE Power Electronics Business Total Quality Management for Suppliers GE Power Electronics Business Total Quality Author: Reviewers: Contributors: Alessandro A. Cervone Technical Manager Component & Reliability Engineering Alicia Scott Title Erika Nannis Title Robert Roessler

More information

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

SQM-H. This Handbook is a summary of the processes and documents of the supplier quality management 1/13 SQM-H Supplier Quality Management Handbook MAHLE Behr - global This Handbook is a summary of the processes and documents of the supplier quality management 1/13 Scope of Application The Supplier Quality

More information

Supplier Quality Requirements

Supplier Quality Requirements Key Elements Procedures # 2 Supplier Quality Requirements Section List of content Page 1.0 Foreword 2 2.0 Definitions and acronyms 2 3.0 Basic Quality Requirements 3 4.0 Part Specific Quality Requirements

More information

The Fulfillment of AS 9100 Rev C Requirements by EnterpriseIQ

The Fulfillment of AS 9100 Rev C Requirements by EnterpriseIQ The Fulfillment of AS 9100 Rev C Requirements by EnterpriseIQ Manufacturers have worked to meet the stringent requirements of AS9100 for decades; the recent introduction of Revision C has further expanded

More information

Supplier quality guideline. VOSS Automotive Group Issue 02.06.2014 Rev00

Supplier quality guideline. VOSS Automotive Group Issue 02.06.2014 Rev00 Supplier quality guideline VOSS Automotive Group Issue 02.06.2014 Rev00 Table of Contents 1. General requirements 1.1 Scope of application 1.2 Quality objectives 1.3 Quality management system 1.4 Supplier

More information

DEFINITIONS. Supply Chain Improvement Program Goals:

DEFINITIONS. Supply Chain Improvement Program Goals: Routine HDX4-51-110 1/8 PURPOSE The purpose of this document is to define the Haldex Supply Chain Improvement Program (SCIP) and associated requirements. SCIP is a tool to monitor and improve the quality

More information

Introduction. Cooper Standard Global Supplier Quality Manual Page 2 of 11

Introduction. Cooper Standard Global Supplier Quality Manual Page 2 of 11 Global Supplier Quality Manual Revision 3 Introduction 1. Purpose: This manual has been created for Cooper Standard s (CS) Production, Prototype and Service Suppliers. The manual includes all CS locations

More information

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

Company Quality Manual Document No. QM Rev 0. 0 John Rickey Initial Release. Controlled Copy Stamp. authorized signature Far West Technology, Inc. ISO 9001 Quality Manual Document No.: QM Revision: 0 Issue Date: 27 August 1997 Approval Signatures President/CEO Executive Vice President Vice President/CFO Change Record Rev

More information

CORPORATE QUALITY MANUAL

CORPORATE QUALITY MANUAL Corporate Quality Manual Preface The following Corporate Quality Manual is written within the framework of ISO 9001:2008 Quality System by the employees of CyberOptics. CyberOptics recognizes the importance

More information

Supplier Guide. Suppliers for production material or services may be qualified for the list in one or more of the following ways:

Supplier Guide. Suppliers for production material or services may be qualified for the list in one or more of the following ways: Supplier Guide Purpose The purpose of this guide is to inform potential and current Suppliers to Jay Industries, Inc. of our policies as well as quality and performance requirements. Application This guide

More information

MINIMUM AUTOMOTIVE QUALITY MANAGEMENT SYSTEM REQUIREMENTS FOR SUB-TIER SUPPLIERS

MINIMUM AUTOMOTIVE QUALITY MANAGEMENT SYSTEM REQUIREMENTS FOR SUB-TIER SUPPLIERS MINIMUM AUTOMOTIVE QUALITY MANAGEMENT SYSTEM REQUIREMENTS FOR SUB-TIER SUPPLIERS CONTENTS 1. CONTROL PLANS 2. PROCESS APPROACH 3. PERFORMANCE 4. INTERNAL AUDITING 5. CONTROL OF NON-CONFORMING PRODUCT 6.

More information

Ege Fren Ege Fren San. ve Tic. A.Ş.

Ege Fren Ege Fren San. ve Tic. A.Ş. Page : 1 / 8 1. Purpose: This manual is formed in order to create a business environment based on a partnership understanding with our suppliers, determine and develop our relationships in this context

More information

Quality management systems

Quality management systems L E C T U R E 9 Quality management systems LECTURE 9 - OVERVIEW Quality management system based on ISO 9000 WHAT IS QMS (QUALITY MANAGEMENT SYSTEM) Goal: Meet customer needs Quality management system includes

More information

Supplier Handbook Terms and Conditions

Supplier Handbook Terms and Conditions * 2 / 7 TABLE OF CONTENTS 1. Section 1 Introduction 1.1. Objective 1.2. Scope 1.3 Contact Information 2. Section 2 Quality Expectations 2.0 Application of This Section 2.1 Change Notification 2.2 Quality

More information

Contents. Management Policy Manual SEM USA Page 2 of 12

Contents. Management Policy Manual SEM USA Page 2 of 12 SEM USA Page 2 of 12 Contents 1. The Schneider Electric Motion USA Management Policy... 3 2. PROCESS INTERACTION... 4 3. COMPANY OBJECTIVES:... 5 4. MANAGEMENT SYSTEM... 6 4.1. General Requirements...

More information

Camar Aircraft Products Co. QUALITY MANUAL Revision D

Camar Aircraft Products Co. QUALITY MANUAL Revision D QUALITY MANUAL Revision D Gujll'y Manual Introduction The purpose of this manual is to describe the Quality Assurance Program implemented by Camar Aircraft Products Co. (hereafter referred to as C.A.P.C.)

More information

ISO/TS 16949:2002 Guidance Document

ISO/TS 16949:2002 Guidance Document ISO/TS 16949:2002 Guidance Document Introduction ISO/TS 16949:2009 emphasizes the development of a process oriented quality management system that provides for continual improvement, defect prevention,

More information

Johnson Controls Automotive Experience Global Supplier Standards Manual Chapter 4 Quality October, 2015

Johnson Controls Automotive Experience Global Supplier Standards Manual Chapter 4 Quality October, 2015 PURPOSE The purpose of the is to communicate Johnson Controls, Inc. (Johnson Controls) requirements to the suppliers in our Automotive Experience Division and Corporate Worldwide Headquarters. It is the

More information

Nuclear Safety Council Instruction number IS-19, of October 22 nd 2008, on the requirements of the nuclear facilities management system

Nuclear Safety Council Instruction number IS-19, of October 22 nd 2008, on the requirements of the nuclear facilities management system Nuclear Safety Council Instruction number IS-19, of October 22 nd 2008, on the requirements of the nuclear facilities management system Published in the Official State Gazette (BOE) number 270 of November

More information

SUPPLIER QUALITY MANAGEMENT SYSTEM QUESTIONNAIRE

SUPPLIER QUALITY MANAGEMENT SYSTEM QUESTIONNAIRE Company Name Street Address City, State, Zip code Phone Number Fax Company Website Email Address ORGANIZATION NAME PHONE NUMBER EMAIL ADDRESS President/CEO General Manager Engineering Manager Production

More information

Management System Procedure. 4.06 30 004 N 4/01/2012 2 of 14

Management System Procedure. 4.06 30 004 N 4/01/2012 2 of 14 4.06 30 004 N 4/01/2012 2 of 14 TABLE OF CONTENTS 1. Introduction 1.1 Policy and Vision 1.2 Purpose 1.3 Scope 1.4 Responsibility 2. Quality System Requirements 2.1 ISO/TS 16949: 2009 and Alternatives 2.2

More information

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

KEBA 2014 We reserve the right to make technical modifications. No liability accepted for information provided. All rights reserved. Supplier Handbook Contact address KEBA AG Headquarters, Gewerbepark Urfahr, A-4041 Linz phone: +43 732 7090-0, fax: +43 732 730910, e-mail: keba@keba.com, www.keba.com KEBA Group worldwide Austria Germany

More information

Schneider Electric Supplier Guide Book. Working together toward operational excellence

Schneider Electric Supplier Guide Book. Working together toward operational excellence Schneider Electric Guide Book Working together toward operational excellence SSQM = SAM + SQM + SPM SSQM Approval Module Assess the Site on management of: Purchasing Quality Supply chain Technical skills,

More information

UL Qualified Firestop Contractor Program Management System Elements. March 13, 2013

UL Qualified Firestop Contractor Program Management System Elements. March 13, 2013 UL Qualified Firestop Contractor Program Management System Elements March 13, 2013 UL and the UL logo are trademarks of UL LLC 2013 Benefits to becoming a Qualified Firestop Contractor Independent, 3 rd

More information

The certification process

The certification process TS004(COS)v01 The certification process for COSMOS standard Standard in force available on www.cosmos-standard.org or sent on request. 1 Contents I. When to apply... 3 II. The different steps in the certification

More information

QUALITY ASSURANCE MANUAL JPM OF MISSISSIPPI, INC.

QUALITY ASSURANCE MANUAL JPM OF MISSISSIPPI, INC. QUALITY ASSURANCE MANUAL JPM OF MISSISSIPPI, INC. Hattiesburg, MS Revision E 01/19/11 Revised to ISO 9001:2008 on July 9, 2009 JPM OF MISSISSIPPI, INC. MANAGEMENT QUALITY POLICY It is the goal of JPM of

More information

PRINTED COPY FOR REFERENCE ONLY

PRINTED COPY FOR REFERENCE ONLY SUPPLIER MANUAL SAGE Automotive Interiors Supplier Manual is effective as of September 23, 2013. All previous editions of this Supplier Manual are obsolete. PRINTED COPY FOR REFERENCE ONLY Page 1 of 17

More information

UNCONTROLLED COPY FOR REFERENCE ONLY

UNCONTROLLED COPY FOR REFERENCE ONLY CLOVER MACHINE AND MFG. 800 MATHEW ST. #101 SANTA CLARA, CA 95050 727-3380 727-7015 fax REVISION: DATE: PAGE 1 OF 45 QUALITY POLICY MANUAL DISTRIBUTION LIST: President Purchasing Manager Vice President

More information

IRIS International Railway Industry Standard

IRIS International Railway Industry Standard English Addendum, 19th June 2008 IRIS International Railway Industry Standard Hier kann ein kleiner Text stehen Hier kann ein kleiner Text stehen Hier kann ein kleiner Text stehen Chapter 1 3 IRIS Certification

More information

This Business Management System Manual is based on ISO 9001:2008 requirements

This Business Management System Manual is based on ISO 9001:2008 requirements Page 1 of 19 (Formerly: Quality Management System Manual) When the ISO 9001:2008 standard is identifying the Quality Manual or Quality Management System, Turbonetics is representing this requirement with

More information

Supplier Quality Requirements Manual

Supplier Quality Requirements Manual Supplier Quality Requirements Manual OPTEK Technology Corporate Headquarters 1645 Wallace Drive Carrollton, TX 75006 Note: The holder of this document is cautioned that the information contained herein

More information

AVNET Logistics & EM Americas. Quality Manual

AVNET Logistics & EM Americas. Quality Manual AVNET Logistics & EM Americas Quality Manual Avnet is committed to ensuring customer satisfaction while meeting all customer and applicable legal, statutory and regulatory requirements. This is accomplished

More information

TRANSPORT FOR LONDON (TfL) LOW EMISSIONS CERTIFICATE (LEC) GUIDANCE NOTES FOR THE COMPANY AUDIT PROCESS. LEC (Company Audit) Guidance Notes

TRANSPORT FOR LONDON (TfL) LOW EMISSIONS CERTIFICATE (LEC) GUIDANCE NOTES FOR THE COMPANY AUDIT PROCESS. LEC (Company Audit) Guidance Notes TRANSPORT FOR LONDON (TfL) LOW EMISSIONS CERTIFICATE (LEC) GUIDANCE NOTES FOR THE COMPANY AUDIT PROCESS LEC (Company Audit) Guidance Notes Glossary of Terms Transport for London (TfL) London Low Emission

More information

PSA Peugeot Citroën Customer-Specific Requirements for use with ISO/TS 16949:2009

PSA Peugeot Citroën Customer-Specific Requirements for use with ISO/TS 16949:2009 PSA Peugeot Citroën Customer-Specific Requirements for use with ISO/TS 16949:2009 First issue: February 2011 Revised: November 2013 1 Purpose of the document The purpose of this document is to describe

More information

Revision Date Author Description of change. 10 07Jun13 Mark Benton Removed Admin. Manager from approval

Revision Date Author Description of change. 10 07Jun13 Mark Benton Removed Admin. Manager from approval Page 2 of 15 Document Revision History Revision Date Author Description of change 10 07Jun13 Mark Benton Removed Admin. Manager from approval 12Feb13 Mark Benton 08 01Oct12 Mark Benton 07 8/30/2012 Refer

More information

14620 Henry Road Houston, Texas 77060 PH: 281-447-3980 FX: 281-447-3988. WEB: www.texasinternational.com QUALITY MANUAL

14620 Henry Road Houston, Texas 77060 PH: 281-447-3980 FX: 281-447-3988. WEB: www.texasinternational.com QUALITY MANUAL 14620 Henry Road Houston, Texas 77060 PH: 281-447-3980 FX: 281-447-3988 WEB: www.texasinternational.com QUALITY MANUAL ISO 9001:2008 API Spec Q1, 9th Edition API Spec 8C 5 Th Edition MANUAL NUMBER: Electronic

More information

ISO 9001:2008 STANDARD OPERATING PROCEDURES MANUAL

ISO 9001:2008 STANDARD OPERATING PROCEDURES MANUAL 8200 Brownleigh Drive Raleigh, NC 27617-7423 Phone: (919) 510-9696 Fax: (919) 510-9668 ISO 9001:2008 STANDARD OPERATING PROCEDURES MANUAL ALLIANCE OF PROFESSIONALS & CONSULTANTS, INC. - 1 - Table of Contents

More information

Quality Management System General

Quality Management System General Audit Date: Quality Management System General Requirement: 4.1 and 4.2.2-QMS General Verify Scope Comments/Evidence/Findings: Verify the Exclusions is applicable and justified How are the processes in

More information

ALL PRODUCTS MFG & SUPPLY

ALL PRODUCTS MFG & SUPPLY ALL PRODUCTS MFG & SUPPLY 618 ANDERSON DRIVE ROMEOVILLE, IL 60446 PHONE: 877-255-8700 FAX: 877-255-8701 WWW. APGASKET.COM QUALITY MANAGEMENT SYSTEM MANUAL DATE: 11/20/12 REVISION 9.1 UNCONTROLLED COPY

More information

ISO 9001 Quality Systems Manual

ISO 9001 Quality Systems Manual ISO 9001 Quality Systems Manual Revision: D Issue Date: March 10, 2004 Introduction Micro Memory Bank, Inc. developed and implemented a Quality Management System in order to document the company s best

More information

FMC Technologies Measurement Solutions Inc.

FMC Technologies Measurement Solutions Inc. Table of Contents 1 Revision History... 4 2 Company... 5 2.1 Introduction... 5 2.2 Quality Policy... 6 2.3 Quality Organization... 6 2.4 Company Processes... 7 3 Scope and Exclusions... 8 3.1 Scope...

More information

SUPPLIER GUIDEBOOK. Rev 1.1

SUPPLIER GUIDEBOOK. Rev 1.1 SUPPLIER GUIDEBOOK CONTENTS INTRODUCTION...5 Beckman Coulter Quality Policy... 5 Danaher Corporation... 5 Beckman Coulter... 5 Preferred Supplier Program... 5 Purpose and Scope... 5 Supplier Management

More information

Quality Supplier Requirements for Beckwith Electric Co., Inc.

Quality Supplier Requirements for Beckwith Electric Co., Inc. Quality Supplier Requirements for Beckwith Electric Co., Inc. This Page Left Intentionally Blank To Our Valued Suppliers: One of the primary goals of Beckwith Electric is to provide the highest Quality

More information

Software Quality Subcontractor Survey Questionnaire INSTRUCTIONS FOR PURCHASE ORDER ATTACHMENT Q-201

Software Quality Subcontractor Survey Questionnaire INSTRUCTIONS FOR PURCHASE ORDER ATTACHMENT Q-201 PURCHASE ORDER ATTACHMENT Q-201A Software Quality Subcontractor Survey Questionnaire INSTRUCTIONS FOR PURCHASE ORDER ATTACHMENT Q-201 1. A qualified employee shall be selected by the Software Quality Manager

More information

Control No: QQM-02 Title: Quality Management Systems Manual Revision 10 07/08/2010 ISO 9001:2008 Page: 1 of 22

Control No: QQM-02 Title: Quality Management Systems Manual Revision 10 07/08/2010 ISO 9001:2008 Page: 1 of 22 ISO 9001:2008 Page: 1 of 22 Central Technologies has developed a Quality Management System, and the associated procedures and work instructions, to be compliant to ISO 9001:2008. Utilizing this Quality

More information

ONTIC UK SUPPLIER QUALITY SURVEY

ONTIC UK SUPPLIER QUALITY SURVEY MAIL-IN / ONSITE This report is intended to furnish data relative to the Suppliers capability to control the quality of supplies and services furnished to Ontic UK. Please complete this Survey and return

More information

Supplier Quality Agreement EK 25

Supplier Quality Agreement EK 25 1. Purpose and Scope of Agreement Supplier Quality Agreement EK 25 1.1. In order to exceed the expectations and ensure the satisfaction of its customers, Benteler is committed to achieving a level of quality

More information

Welcome! Frank Teleso. Quality Manager

Welcome! Frank Teleso. Quality Manager Welcome! We appreciate your interest in Excelsior s Quality Management System. The objective of this document is to provide a quick method for you to do a preliminary quality qualification of Excelsior

More information

Comparison ISO/TS 16949 (1999) to VDA 6.1 (1998)

Comparison ISO/TS 16949 (1999) to VDA 6.1 (1998) 1 APPLICABILITY VDA 6.1: Section: 3.1; 7 new: In addition to the applicability for supplier sites for production, services and their subcontractors for: products and production materials, or services like

More information

VDA6.3 Process Audit Webinar 1 st April 2014. Paul Hardiman Qualified VDA6.3 trainer

VDA6.3 Process Audit Webinar 1 st April 2014. Paul Hardiman Qualified VDA6.3 trainer VDA6.3 Process Audit Webinar 1 st April 2014 Paul Hardiman Qualified VDA6.3 trainer During presentations (11:00 11:30) everyone will be muted so that only the presenter will be heard. The presentation

More information

PRO-SUPPLIER PERFORMANCE MANUAL PROCEDURE Supplier Performance Manual REVISION L December 7, 2015

PRO-SUPPLIER PERFORMANCE MANUAL PROCEDURE Supplier Performance Manual REVISION L December 7, 2015 APPROVAL Procedure Section Process Owner Approval 1.0 Letter of Introduction 2.0 Global Competitiveness 3.0 Supply Chain Contact List 4.0 Quality Policy Statement 5.0 Quality Systems Qualifications 6.0

More information

Supplier Quality Assurance Requirements Manual

Supplier Quality Assurance Requirements Manual 1701 West Tacoma Broken Arrow, Ok. 74012 Supplier Quality Assurance Requirements Manual Approved: Bryan Sanderlin President/COO/CEO OSECO, Inc. Darrel Bilke Quality Assurance Manager OSECO, Inc. 1 Record

More information

Cartel Electronics. AS 9100 Quality Systems Manual

Cartel Electronics. AS 9100 Quality Systems Manual Cartel Electronics AS 9100 Quality Systems Manual 1900 C Petra Lane Placentia, California 92870 Introduction Cartel Electronics, as a global supplier to the aviation, space, and space industries, has developed

More information

Surgi Manufacturing Quality Manual

Surgi Manufacturing Quality Manual Surgi Manufacturing Page 1 of 18 Approvals: QA: Eng. Mgt. : A Date: 18Aug98 1. Introduction... 4 1.1 Scope... 4 1.2 Purpose... 4 1.3 Authority... 4 1.4 Issue of the Manual... 4 1.5 Amendments... 4 1.6

More information

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

Specialties Manufacturing. Talladega Castings & Machine Co., Inc. ISO 9001:2008. Quality Manual Specialties Manufacturing Talladega Castings & Machine Co., Inc. ISO 9001:2008 This document is the property of TMS and may not be reproduced, wholly, or in part, without the express consent of TMS. Rev.

More information

Quality Management System Manual

Quality Management System Manual Quality Management System Manual Assurance ISO / AS Manual Quality Management System EXCEEDING ALL EXPECTATIONS Since our inception in 1965, Swiss-Tech has supplied the medical, aerospace, hydraulic, electronic

More information

Derbyshire Trading Standards Service Quality Manual

Derbyshire Trading Standards Service Quality Manual Derbyshire Trading Standards Service Quality Manual This Quality Manual has been developed to give a broad outline of how the Trading Standards Division s range of services comply with the requirements

More information

DEC STD 017-2 - ISO 9002 - Quality Systems - Model for Quality Assurance in Production and Installation

DEC STD 017-2 - ISO 9002 - Quality Systems - Model for Quality Assurance in Production and Installation Digital Internal Use Only DEC STD 017-2 - ISO 9002 - Quality Systems - Model for Quality Assurance in Production and Installation DOCUMENT IDENTIFIER: A-DS-EL00017-02-0000 Rev A, ABSTRACT: This standard

More information

Supplier Quality Manual Quality requirements SCG-STD-006-01

Supplier Quality Manual Quality requirements SCG-STD-006-01 Supplier Quality Manual Quality requirements SCG-STD-006-01 10/10/2010 TRANSPORT INTRODUCTION External parts from suppliers highly contribute to high quality products, solutions and services we have to

More information

QUALITY POLICY MANUAL Document: 01-090000 Revision: E Effective Date: January 15, 2010

QUALITY POLICY MANUAL Document: 01-090000 Revision: E Effective Date: January 15, 2010 Section i INTRODUCTION QUALITY POLICY STATEMENT: The purpose of our business is to provide continuity of electrical power to keep businesses in business. We do this by helping clients solve their power

More information

GARDNER AEROSPACE SUPPLIER QUALITY REQUIREMENTS MANUAL

GARDNER AEROSPACE SUPPLIER QUALITY REQUIREMENTS MANUAL GARDNER AEROSPACE SUPPLIER QUALITY REQUIREMENTS MANUAL Issue Number: 1 Issue Date: 12/9/14 1 of 19 Contents Revision Summary... 4 1.0 Introduction... 5 2.0 Supplier Quality System Requirements... 6 3.0

More information

QP-740. Supplier Management Handbook

QP-740. Supplier Management Handbook QP-740 Supplier Management Handbook Revision H Revision Date Reason Signature - 2/02/08 Initial Release Avis Rosenfield A 12/10/10 Complete update Ritchie Lacson B 4/14/11 Add sections: 6.4, 6.5, 9.9,

More information

Quality System Manual

Quality System Manual Quality System Manual Joe Coatter 9/23/15 President - Joe Coatter Date Bill Gareis ISO/TS Management Representative - Bill Gareis 9/23/15 Date Revision Status: Revision # 7 (9-23-15) QUA-0003 4.2.2 SECTION

More information

Valuable Metrics for Successful Supplier Management

Valuable Metrics for Successful Supplier Management Valuable Metrics for Successful Supplier Management Stringent global trade and product safety regulations have been increasingly enforced, driving organizations to seek absolute visibility across the supply

More information

STEEL fabrication quality SySTEmS guideline

STEEL fabrication quality SySTEmS guideline STEEL fabrication quality systems guideline Copyright 2002 by Canadian Institute of Steel Construction All rights reserved. This book or any part therof must not be reproduced in any form without written

More information

Integrated Supplier Quality Requirements

Integrated Supplier Quality Requirements Integrated Supplier Quality Requirements ISQ-001-QM November 1, 2013 Revision C The controlled and current version of this document, and all referenced documents, are available on www.navistarsupplier.com.

More information

Supplier Quality Assurance

Supplier Quality Assurance Supplier Quality Assurance Preface We strive to continually improve our process performance by meeting quality objectives. It is imperative that our suppliers operate under the zero defects and 100% on

More information

Quality Manual. ISO/TS 16949:2009 Quality Management System. Sensing and Control

Quality Manual. ISO/TS 16949:2009 Quality Management System. Sensing and Control Sensing and Control ISO/TS 16949:2009 Quality Management System CORPORATE HEADQUARTERS: OPTEK Technology 1645 Wallace Drive Carrollton, TX 75006 MANUFACTURING: Optron de Mexico Avenue Rio Bravo #1551 Parque

More information

Supplier Quality Management System Audit Checklist (ISO 9000:2000, TS 16949:2002)

Supplier Quality Management System Audit Checklist (ISO 9000:2000, TS 16949:2002) Supplier Quality Management System Audit Checklist (ISO 9000:2000, TS 16949:2002) Supplier: Plant/Location: Date: Audit Team: Scope of Audit: Number of C.A.R. s: Corrective Action Due: Potential suppliers

More information

SUPPLIER QUALITY SELF AUDIT & QUESTIONNAIRE FORM

SUPPLIER QUALITY SELF AUDIT & QUESTIONNAIRE FORM Fuji Autotech USA, LLC Walton, KY 41094 DATE: SUPPLIER QUALITY SELF AUDIT & QUESTIONNAIRE FORM DUNS# Supplier Name Complete Mailing Address Complete Shipping Address (if different then mailing address)

More information

Supplier Quality Requirements and Clauses

Supplier Quality Requirements and Clauses Supplier Quality Requirements and Clauses Supplier Quality Requirements General The following Quality Notes (QN01 through QN19) apply to and form a part of all Purchase Orders issued by Advanced Conversion

More information

Supplier Quality System Requirements

Supplier Quality System Requirements AUTOMOTIVE AXLES LIMITED Supplier Quality System Requirements Supplier Quality System Requirement, New Release, January 20, 2014 Page 1 AAL QUALITY POLICY We shall be a world class Automotive Tier I organisation

More information

Implementing an ISO 9001 Quality Management System

Implementing an ISO 9001 Quality Management System Implementing an ISO 9001 Quality Management System ETI Group This guide to implementing an ISO 9001 Quality Management System (QMS) was prepared by ETI Group. The guide is based on our experiences assisting

More information

Supplier Quality Assurance Requirements Manual

Supplier Quality Assurance Requirements Manual 12716 EAST PINE STREET TULSA, OK 74116 Supplier Quality Assurance Requirements Manual Approved: Mike Collins Quality Assurance Manager Precise Machining & Manufacturing 1 Record of Revisions Revision D

More information

Donaldson Buys Value SBOSS. Donaldson Supplier Business Operating System Standard (SBOSS)

Donaldson Buys Value SBOSS. Donaldson Supplier Business Operating System Standard (SBOSS) Donaldson Supplier Business Operating System Standard () Supplier Business Operating System Standard () INTRODUCTION DCI is a multi-plant manufacturing company serving several different markets. These

More information

VELUX General Quality Requirements

VELUX General Quality Requirements VELUX General Quality Requirements Introduction In VELUX we want to work towards zero defects and it is our belief that the quality of the products is best secured at our suppliers thereby enabling ship

More information

Global Supplier Quality Manual February 2014

Global Supplier Quality Manual February 2014 Global Supplier Quality Manual February 2014 Table of content Introduction 3 1. Scope and purpose 4 2. Quality alignment 4 3. Quality Management System expectation 4 4. E-Business, communication and language

More information

0. 0 TABLE OF CONTENTS

0. 0 TABLE OF CONTENTS QUALITY MANUAL Conforming to ISO 9001:2000 0. 0 TABLE OF CONTENTS Section Description ISO 9001 Clause Page 0 TABLE OF CONTENTS n/a 2 1 PIMA VALVE, INC. DESCRIPTION n/a 3 2 QUALITY MANUAL DESCRIPTION 4.2.2

More information

Quality Manual. DuraTech Industries, Inc. 3216 Commerce Street La Crosse, WI 54603 MANUAL SERIAL NUMBER 1

Quality Manual. DuraTech Industries, Inc. 3216 Commerce Street La Crosse, WI 54603 MANUAL SERIAL NUMBER 1 Quality Manual Approval Page Document: QA1000 Issue Date: 5/29/1997 Page 1 of 17 Revision Date: 5/20/2013 DuraTech Industries, Inc. 3216 Commerce Street La Crosse, WI 54603 MANUAL SERIAL NUMBER 1 This

More information

Logistics Agreement. between. SMA Solar Technology AG Sonnenallee 1 34266 Niestetal Germany. hereinafter referred to as SMA. and.

Logistics Agreement. between. SMA Solar Technology AG Sonnenallee 1 34266 Niestetal Germany. hereinafter referred to as SMA. and. between SMA Solar Technology AG Sonnenallee 1 34266 Niestetal Germany hereinafter referred to as SMA and Supplier hereinafter referred to as Supplier jointly referred to as Parties Version 2 2014-09-18

More information

Supplier Rating System

Supplier Rating System Supplier Rating System Supplier Manual Presented by Admiral Tool & Manufacturing Purchasing and Quality WI-PU-06-002 Rev. Lev. 003 Rev. Date 02/06/2003 1 Table of Contents Introduction 3 Scoring Criteria

More information

QUALITY CONTROL MANUAL

QUALITY CONTROL MANUAL QUALITY CONTROL MANUAL TABLE OF CONTENTS PREFACE I II III IV Title Page Table of Contents Information Page Revision Log SECTION DESCRIPTION 1.0 Introduction 2.0 Organization 3.0 Organization Chart 4.0

More information

1029 A West State Blvd. Ft Wayne, Indiana 46808 QUALITY MANAGEMENT SYSTEM POLICY MANUAL. Based on: ISO 9001:2008 AND ISO/TS 16949:2009.

1029 A West State Blvd. Ft Wayne, Indiana 46808 QUALITY MANAGEMENT SYSTEM POLICY MANUAL. Based on: ISO 9001:2008 AND ISO/TS 16949:2009. 1029 A West State Blvd. Ft Wayne, Indiana 46808 QUALITY MANAGEMENT SYSTEM POLICY MANUAL Based on: ISO 9001:2008 AND ISO/TS 16949:2009 Authorized By: Randy Shepherd VP of Quality Issue Date: March 1, 2004

More information

Quality Agreement Template

Quality Agreement Template Quality Agreement Template Prepared by Dan O Leary Ombu Enterprises, LLC 3 Forest Ave. Swanzey, NH 03446 603-209-0600 This document is intended to form the basis for a Supplier Agreement. The document

More information

MEDFORD FABRICATION CSC, INC. Quality System Manual. Date of issue: 03/25/2010 Revision : F

MEDFORD FABRICATION CSC, INC. Quality System Manual. Date of issue: 03/25/2010 Revision : F MEDFORD FABRICATION CSC, INC Quality System Manual Date of issue: 03/25/2010 Revision : F Table of Contents System Description 1.0 Introduction 2.0 Company Quality Policy 3.0 Organization Charts 4.0 Quality

More information

RTP s NUCLEAR QUALITY ASSURANCE PROGRAM

RTP s NUCLEAR QUALITY ASSURANCE PROGRAM RTP s NUCLEAR QUALITY ASSURANCE PROGRAM RTP operates under one quality program, whether you purchase products that are commercial grade, nuclear safety-related or industrial safety compliant (IEC 61508).

More information

Manual ETEL. - Quality Management - Occupational Health and Safety - Environmental Protection

Manual ETEL. - Quality Management - Occupational Health and Safety - Environmental Protection Manual ETEL - Quality Management - Occupational Health and Safety - Environmental Protection This Manual is the property of ETEL S.A. It may be neither reproduced nor passed on to third parties. This document

More information

Quality Management System MANUAL. SDIX, LLC Headquarters: 111 Pencader Drive Newark, Delaware 19702

Quality Management System MANUAL. SDIX, LLC Headquarters: 111 Pencader Drive Newark, Delaware 19702 Quality Management System MANUAL SDIX, LLC Headquarters: 111 Pencader Drive Newark, Delaware 19702 Doc. No. G5500 Rev. 9.2 Status : APPROVED Effective: 9/25/2015 Page 2 of 23 Quality Manual Table of Contents

More information

MTAT.03.243 Software Engineering Management

MTAT.03.243 Software Engineering Management MTAT.03.243 Software Engineering Management Lecture 17: Other SPI Frameworks and QM Systems Dietmar Pfahl Spring 2014 email: dietmar.pfahl@ut.ee Structure of Lecture 17 Other SPI Frameworks People CMM

More information

Frequently Asked Questions. Unannounced audits for manufacturers of CE-marked medical devices. 720 DM 0701-53a Rev 1 2014/10/02

Frequently Asked Questions. Unannounced audits for manufacturers of CE-marked medical devices. 720 DM 0701-53a Rev 1 2014/10/02 Frequently Asked Questions Unannounced audits for manufacturers of CE-marked medical devices 720 DM 0701-53a Rev 1 2014/10/02 What is an unannounced audit?... 6 Are unannounced audits part of a new requirement?...

More information

Quality, Environmental, Health and Safety Manual Toshiba International Corporation

Quality, Environmental, Health and Safety Manual Toshiba International Corporation Quality, Environmental, Health and Safety Manual Toshiba International Corporation Doc. No. QEHS 001 Rev. 19 (12/12) Title: Prepared By: Revision No.: Table of Contents and Cross Reference Ken Mori/Homer

More information

QUALITY MANUAL REVISION RECORD

QUALITY MANUAL REVISION RECORD Page 2 of 31 REVISION RECORD Date Rev Description Jun 18, 2007 N/C Original Issue Sep 16, 2009 A Update to ISO 9001:2008 Standard. Feb 04, 2010 B Revised exclusions, removed (Except 7.3.7 from the exclusion

More information

Presentation by BSI on the main changes to the IATF ISO/TS 16949 certification scheme

Presentation by BSI on the main changes to the IATF ISO/TS 16949 certification scheme Presentation by BSI on the main changes to the IATF ISO/TS 16949 certification scheme ISO/TS 16949 IATF Scheme rules 4 th edition areas that impact BSI Clients Copyright 2014 BSI. All rights reserved.

More information

CONTROL PROCESS NATURAL ORIGIN AND ORGANIC CANDLES AND HOME FRAGRANCES

CONTROL PROCESS NATURAL ORIGIN AND ORGANIC CANDLES AND HOME FRAGRANCES TS004(GPA)v03en v25/11/2015 CONTROL PROCESS NATURAL ORIGIN AND ORGANIC CANDLES AND HOME FRAGRANCES The aim of the present document is to describe the key steps of the control process. This document is

More information

Supplier Quality Agreements

Supplier Quality Agreements Supplier Quality Agreements Dan O Leary CBA, CQA, CQE, CRE, SSBB, CIRM President Ombu Enterprises, LLC Dan@OmbuEnterprises.com www.ombuenterprises.com 603-209-0600 1 Speaker Biography Dan O Leary Dan O

More information

FMP SUPPLIER QUALITY MANAGEMENT PROGRAM

FMP SUPPLIER QUALITY MANAGEMENT PROGRAM FMP SUPPLIER QUALITY MANAGEMENT PROGRAM Table of Contents 1.0 Introduction 4 1.1 Scope 4 1.2 Purpose 4 2.0 Quality System Requirements 5 2.1 Specific Requirements 5 2.2 General Quality System Requirements

More information

OVERVIEW OF THE PREQUALIFICATION OF DIAGNOSTICS ASSESSMENT PROCESS. Prequalification of Diagnostics

OVERVIEW OF THE PREQUALIFICATION OF DIAGNOSTICS ASSESSMENT PROCESS. Prequalification of Diagnostics D i a g n o s t i c s a n d L a b o r a t o r y T e c h n o l o g y OVERVIEW OF THE PREQUALIFICATION OF DIAGNOSTICS ASSESSMENT PROCESS Prequalification of Diagnostics PQDx_007 v3 20 April 2010 Table of

More information

Standard conditions of purchase

Standard conditions of purchase Standard conditions of purchase 1 OFFER AND ACCEPTANCE 2 PROPERTY, RISK & DELIVERY 3 PRICES & RATES The Supplier shall provide all Goods and Services in accordance with the terms and conditions set out

More information

Camber Quality Assurance (QA) Approach

Camber Quality Assurance (QA) Approach Camber Quality Assurance (QA) Approach Camber s QA approach brings a tested, systematic methodology, ensuring that our customers receive the highest quality products and services, delivered via efficient

More information