General Motors Globális Gyártási Rendszer General Motors Global Manufacturing System General Motors Powertrain – Magyarország Kft. Dátum: 2008. Április 16 Előadó: Kovács János Minőségügyi Igazgató Cél: Minőségügyi alapelvek alkalmazásának bemutatása a GM Globális Gyártási Rendszer ismertetésén keresztül Első előadás témái: A vevő fogalma, vevői elégedettség Termékminőségi követelmények Termelési folyamat jóváhagyás Második előadás témái: Folyamatközi ellenőrzés és folyamat igazolás Minőség visszajelzés - előrejelzés rendszere Minőségirányítási rendszer 2 Globális Gyártási Rendszer General Motors-Global Manufacturing System 3 4 Folyamatközi ellenőrzés és folyamat igazolás (In-Process Control and Verification) The GMS element “In-Process Control & Verification” incorporates the intent and purpose of the BIQ motto: Quality expectations are achieved in each process to ensure defects are not passed on to downstream process. 5 Folyamatközi ellenőrzés és folyamat igazolás (In-Process Control and Verification) Customer satisfaction achievement Customer satisfaction is achieved through three sub-elements: • Prevention: avoid defects or non-standards occurring • Detection: identify when defects or non-standards have occurred • Containment: assure defects or non-standards are not passed on 6 Folyamatközi ellenőrzés és folyamat igazolás (In-Process Control and Verification) Benefits To External customers (people buying our vehicle). • Protect Customers from sub-standard vehicle quality. • Assure customer satisfaction To Internal customer (downstream operation). • Prevent major repair and rework by detecting a non-conformity early in the • Prevent the flow of defects from department to department and station to station process. To Internal customer (from supplier). • Protect Team Members from non-compliant parts from suppliers through and prompt containment during spills. advanced quality planning 7 Folyamatközi ellenőrzés és folyamat igazolás (In-Process Control and Verification) 8 Folyamatközi ellenőrzés és folyamat igazolás (In-Process Control and Verification) Process Equipment Capability Reviews (Prevention) Periodic checks (typically monthly), are conducted to identify trends or shifts in capability over periods of time. 1. Identify process equipment with high risk/impact 2. Conduct initial capability confirmation 3. Conduct regular scheduled reviews to confirm capability 4. Implement corrective action as required 9 Folyamatközi ellenőrzés és folyamat igazolás (In-Process Control and Verification) Detection Purpose of Detection: To make non-standard conditions in the manufacturing process visible - identify when defects or non-standards have occurred. This supports the “Do Not Accept” element of the quality motto: inspection process that confirms quality as soon as possible following manufacture measures the output of the manufacturing process alerts organization to out of standard conditions supports containment and provides input into continuous improvement 10 Folyamatközi ellenőrzés és folyamat igazolás (In-Process Control and Verification) Quality Check System Update Internal/external ‘Customers’ are monitored for feedback: Where there is an indication of defect flow-out through the Verification process, a systematic analysis will be conducted; typically for: 11 Folyamatközi ellenőrzés és folyamat igazolás (In-Process Control and Verification) Inspection Frequencies of Critical Operations The quality check system must be established in consideration of the ‘Supplier-Customer’ relationship. Inspection frequencies must be established by each ‘supplier’ that prevent shipping defects to downstream ‘customers’. This is a requirement for safety & compliance items, key characteristics and for issues that will significantly impact the next process or customer. 12 Folyamatközi ellenőrzés és folyamat igazolás (In-Process Control and Verification) Independent Repair Confirmation During a repair, the risk for a discrepancy to occur is increased - many aspects of the repair operation are non-standard: Any documented repair must be verified by Repair Confirmation (both on- and off-line) Repair Confirmation must be conducted independently (e.g. by Quality). Standardized work (non-cyclic) should be used for the confirmation process – quality standards must be available. Appropriate training and knowledge of standards must be developed to conduct or confirm repairs. Repair confirmation should be as close to the repair process as possible. Repair confirmation can be conducted by man or machine. 13 Folyamatközi ellenőrzés és folyamat igazolás (In-Process Control and Verification) Using Andon To Stop The Process: Work Station Team has the ability to stop the line and complete standardized work in station. If the Team Member has a quality issue within their standardized work they activate the Andon system to: initiate a call for help through station light, Andon board, and melody empower the Team Member to stop line & organization responds to provide support stop at FPS (Fixed Position Stop) to contain and complete the repair where Andon is not available the principles still apply 14 Folyamatközi ellenőrzés és folyamat igazolás (In-Process Control and Verification) Alarm & Escalation Processes When a defect is detected, feedback to the appropriate team or individual will be given by using a communication system. The alarm is raised by using audio/visual signals (e.g. Andon). The alarm process directs the support functions to: ‘Go and See’ the problem Apply containment to prevent further flow of defects Initiate problem solving 15 Folyamatközi ellenőrzés és folyamat igazolás (In-Process Control and Verification) Containment Purpose of Containment: •The achievement of customer expectations relies on a method to contain defects within the manufacturing process, and implement corrections to protect the next/downstream customer. •This supports the “Do Not Ship” element of the quality motto: vehicle delivery to the customer Powertrain and MFD plants to vehicle assembly external supplier to the manufacturing plant internal departments (e.g. between body, paint and GA) between work stations within a department 16 Folyamatközi ellenőrzés és folyamat igazolás (In-Process Control and Verification) Containment Process Overview 17 Folyamatközi ellenőrzés és folyamat igazolás (In-Process Control and Verification) Summary Standardized work is performed in every process and includes the required quality checks. Process control activities are implemented on equipment to control variation on a daily basis and maintain capability over a period of time. Detection confirms the manufacturing process and ensures both internal (Production Team Members) and External Customers (people who buy our products) are receiving products that meet or exceed the quality standards. A process is in place to contain defects within the manufacturing process and implement permanent corrective actions that are verified as being effective. 18 Kockázatelemzési és hiba-megelőzési módszer, PFMEA (Process Failure and Effect Analysis) Purpose of this procedure: Investigation, documentation and if necessary reduction of the risk potential (Risk Priority Number-RPN) for all production processes RISK PRIORITY NUMBER S x O x D = RPN • • • • S = Severity O = Occurrence D = Detection RPN = Risk Priority Number* * 1 = Lowest 1000 = Highest 19 Kockázatelemzési és hiba-megelőzési módszer, PFMEA (Process Failure and Effect Analysis) Potential failure mode: What things have gone wrong ? What things could go wrong ? Effects of failure: What does a failure mean to the next operation, the assy plant, the final customer? Potential Cause of failure: Root cause what has gone wrong in the past Brainstorm what could cause failures? Current controls: What do we do today to prevent the defect from occurring and getting to our customer ? Recommended actions: If current controls are not 100% effective, what actions should be taken ? 20 Kockázatelemzési és hiba-megelőzési módszer, PFMEA (Process Failure and Effect Analysis) Very high severity ranking when a potential failure mode affects safe vehicle operation and/or involves noncompliance with government regulation without warning. Or may endanger operator (machine or assembly) without warning Very high severity ranking when a potential failure mode affects safe vehicle operation and/or involves noncompliance with government regulation with warning. Or may endanger operator (machine or assembly) with warning Vehicle / item inoperable (loss of primary function). Or 100% of product may have to be scrapped, or vehicle / item repaired in repair department with a repair time greater than one hour. Vehicle / item operable but at a reduced level of performance. Customer very dissatisfied. 10 Very High: Persistent Failures Or product may have to be sorted and portion (less than 100%) scrapped, or vehicle / item repaired in repair department with a repair time between a half-hour and an hour. ≥100 per thousand per pieces per pieces 9 50 per thousand per pieces per pieces 8 20 per thousand per pieces per pieces High: Frequent Failures 7 10 per thousand per pieces Absolute Almost certainty Impossibl of none detection. A B C Ranking Criteria Detection Manufacturing Assembly Effect Inspection Types Ranking Customer Effect Probability This ranking results w hen a potential failure m ode results in a final custom er and/or a m anufacturing/assem bly plant defect. The final custom er should alw ays be considered first. If both occur, use the higher of the tw o severities. Detection Suggested Range of Detection Methods Occurence Likely Failure Rates Severity X Cannot detect or is not checked. 9* Controls Very will Remote probably not detect. X Control is achieved with indirect or random checks only. 9 8 Controls have poor Remote chance of detection. X Control is achieved with visual inspection only. 8 7 Controls have poor Very Low chance of detection. X Control is achieved with double visual inspection only. 7 10 10 21 Kockázatelemzési és hiba-megelőzési módszer, PFMEA (Process Failure and Effect Analysis) Or a portion (less than 100%) of the Vehicle / item operable but Comfort product, may have to scrapped with Moderate / Convenience item(s) inoperable. no sorting, or vehicle / item repaired Customer dissatisfied. in repair department with a repair time less than a half-hour. Low Or 100% of product may have to be Vehicle / item operable but Comfort reworked, or a vehicle / item repaired / Convenience item(s) operable at a offline but does not go to repair reduced level of performance. department. Fit and Finish/Squeak and Rattle item does not conform. Defect Very Low noticed by most customers (greater than 75%) Minor Very Minor None Or the product may have to be sorted, with no scrap,and a portion (less than 100%) reworked. 5 per thousand per pieces 6 5 Moderate: Occasion 2 per thousand al per pieces Failures Fit and Finish/Squeak and Rattle item does not conform. Defect noticed by 50% of customers. Or a portion (less than 100%) of the product may have to be reworked, with no scrap, on-line but out-ofstation. Fit and Finish/Squeak and Rattle item does not conform. Defect noticed by discriminating customers (less than 25%). Or a portion (less than 100%) of the product may have to be reworked, with no scrap, on-line but out-ofstation. 2 No discernible effect. Or slight inconvenience to operation or operator, or no effect. 1 3 Low: Relatively Few Failures Remote: Failure is Unlikely Low Controls may detect. 5 Controls Moderate may detect. 4 Controls have a Moderatel good y High chance to detect. 0,5 per thousand per pieces 3 High Controls have a good chance to detect. 0,1 per thousand per pieces 2 Very High Controls almost certain to detect. ≤ 0,01 per thousand per pieces 1 Very High certain 1 per thousand per pieces 4 6 X X Control is achieved with charting methods, such as SPC [Statistic Process Control] X Control is based on variable gauging after parts have left the station, or Go/No Go gauging performed on 100% of the parts after parts have left the station. X Error detection in subsequent operations, or gauging performed on setup and first-piece check (for set-up causes only) X X Error detection in-station, or error detection in subsequent operations by multiple layers of acceptance: supply, select, install, verify. Cannot accept discrepant part. X X Error detection in-station (automatic gauging with automatic stop feature). Cannot pass discrepant part. X Discrepant parts cannot be made because item has been error-proofed by process/product design. Controls X to detect. Inspection Types: A = Error-proofed B = Gauging C = Manual Inspection 22 Kockázatelemzési és hiba-megelőzési módszer, PFMEA (Process Failure and Effect Analysis) Dehydration Function: 5 Drink cold beer 1 Requirement: Increased irritability 10 Wrong brand 3 RPN Daily inventory (layered audit) 6 60 Random Sampling visual inspection 8 160 Registered complaints - Warning 4 120 Current Process Controls PREVENTION Automatic restocking system Thermostatically controlled Temperature too high 2 environment -a.k.a. refrigerator Still thirsty Satisfy thirst Not enough available DETECTION Potential Effects of Failure Potential Cause Mechanism of Failure OCCURANCE Process Function and Requirements Potential Failure Mode SEVERITY A practical example – „with user friendly logistic solution „ Remove people who don’t like my favorite brand of beer from invitation list DETECTION 23 Minőség visszajelzés - előrejelzés rendszere (Quality Feedback/Feedforward) Definition The communication of quality expectations and results between customers and suppliers through standardized communication pathways. Purpose: To ensure that information on quality reaches those who need it. 24 Minőség visszajelzés - előrejelzés rendszere (Quality Feedback/Feedforward) Feed Information Forward Internal and external suppliers communicate known/potential problems and/or problem solving status to their customers in a timely manner. This provides the customer with sufficient lead time to react to upcoming changes and take appropriate measures. 25 Minőség visszajelzés - előrejelzés rendszere (Quality Feedback/Feedforward) Feed Information Back Internal and external customers communicate known/potential problems and/or problem solving resolution to their suppliers in a timely manner. This provides the supplier with sufficient lead time to react to customer issues and take appropriate measures. 26 Minőség visszajelzés - előrejelzés rendszere (Quality Feedback/Feedforward) Example: Inspection Ticket Build and quality status of each vehicle is communicated to downstream processes. 27 Minőség visszajelzés - előrejelzés rendszere (Quality Feedback/Feedforward) Summary Feedback/Feedforward promotes the communication of quality expectations and results between customers and suppliers through: • Clearly defining customer/supplier communication requirements • Defining timing, content, and format of information • Establishing metrics and the subsequent management process • Effective implementation of the Feedback/Feedforward communication tools • Problem identification, input into the plant problem solving countermeasure follow up process and 28 Minőségirányítási rendszer (Quality System Management) Who is responsible for Quality? • Team work is absolutely essential to deliver world-class quality. Everyone! Quality is a shared responsibility 29 Minőségirányítási rendszer (Quality System Management) Quality Function Resource Allocation Manufacturing and quality resources are allocated to support the quality system and interface with engineering. Each area requires sufficient resources to properly focus on supporting production and driving continuous improvement through P-D-C-A. 30 Minőségirányítási rendszer (Quality System Management) Quality Function Resource Allocation Resource allocation needs to consider the quality and production components that are required to support the team member. 31 Minőségirányítási rendszer (Quality System Management) Role of the Functions Within the Plant Quality Department 32 Minőségirányítási rendszer (Quality System Management) Summary Quality System Management provides the supporting structure and framework for the implementation of the quality system and ongoing improvement to the quality of our products through: •Establishment and implementation of a strategic quality plan for the organization •Allocation of manufacturing and quality resources to support the quality plan •Development of an organization for quality that incorporates the “Planning”, “Doing” and “Checking” functions into their structure •Identification of requirements for documentation, procedures, practices and assessments •Integration of both quality and manufacturing BPD’s at all levels of the organization 33 Folyamatközi ellenőrzés és folyamat igazolás (In-Process Control and Verification) Ellenőrző kérdések: 1. Mi a beépített minőségi előírások jelmondat? (What is the motto of the BIQ?) 2. Mi az a három alapelv amivel ki lehet vívni a vevői elégedettséget? (What is the three principle wherewith you can achieve the costumer satisfaction?) 3. Miknek a folyamatos ellenőrzésével és milyen módon lehet a hiba előfordulásának megelőzését támogatni? (What monitoring and what way can you support the prevention with?) 4. Mire használják az Andon rendszert, és mi történik a működtetésekor? (What is the Andon system for and what happen when it is activated?) 34 Kockázatelemzési és hiba-megelőzési módszer, PFMEA (Process Failure and Effect Analysis) Ellenőrző kérdések: 1. Mi a PFMEA és mit támogat a quality jelmondatban? (What is the PFMEA and what supports in the quality motto?) 2. Mit jelent a súlyosság az RPN szám meghatározásánál? (What is the severity at the calculation of the RPN number?) 35 Minőség visszajelzés - előrejelzés rendszere (Quality Feedback/Feedforward) Ellenőrző kérdések: 1. Mi a meghatározása a minőség visszajelzés-előrejelzés rendszerének? (What is the definition of the Quality Feedback/Feedforward system?) 2. Milyen információkat kell továbbítania a szállítónak a vevő felé? (What information have to be forwarded to the costumer by supplyer?) 3. Milyen információkat továbbít a vevő a szállító felé? (What information is forwarded back to the supplier?) 36 Minőségirányítási rendszer (Quality System Management) Ellenőrző kérdések: 1. Milyen fő funkciók vannak a Quality osztályon belül a GMS szerint? (What functions are there in the Quality Department according to the GMS?) 2. Mi a „Quality Engineering” feladata? (What is Quality Engineering responsible for?) 3. Mi a „Quality Confirmation” feladata? (What is Quality Confirmation responsible for?) 4. Mi a „Quality Assurance” feladata? (What is Quality Assurance responsible for?) 37 Köszönöm a figyelmet! Thank you for your attention! 38