Quality Assurance Services, Inc. (QAS) provides quality control services including inspection, sorting, containment, and rework to meet ISO 9001:2008 standards. Its mission is to be a successful supplier committed to continuous improvement, customer satisfaction, and long-term partnerships. QAS inspects non-conforming products using customer requirements and production schedules, containing defects and reworking components as needed. Key metrics include customer concerns, reporting errors, and no bill hours to ensure effectiveness.
Jim Sylph addresses Ethics Forum participants at the Singapore Accountancy Convention 2014. He the discusses the public's expectations of the profession, recent fraud and regulatory activity, and the how the profession is responding. He also gives an update on the work of the International Ethics Standards Board for Accountants (IESBA) in developing and maintaining the Code of Ethics for Professional Accountants, designed for worldwide application.
How to Perform a Successful Internal Quality AuditGreenlight Guru
You already know internal quality audits are required by both FDA 21 CFR Part 820 and ISO 13485.
You also probably already know they are a big hassle to conduct.
What you might not know is that they are one of the most powerful weapons at your disposal for preventing 483's and observations.
Why?
Because they are one of the most effective and efficient ways to make sure you and your team are always prepared if FDA or NB decided to show up unexpectedly.
So how do you “establish” the right procedures? How do you ensure your auditor is competent and properly qualified? And what do you do if you find non-conformances?
View this presentation by our guest Kyle Rose, President at Rook Quality Systems, where you will find the answers to all those questions and more.
Specifically, you will learn:
- How to conduct an effective internal quality audit based on process identification, sampling and questioning
- How to plan a internal quality audit and develop an audit schedule
- How to find and use competent and qualified auditors
- Why certain auditors shouldn’t audit certain areas
- How to properly report the findings of your internal quality audit
- How to concisely document non-conformances
- How to determine what needs corrective actions and how to follow up on them
ISO17025 Accreditation Procedures and Process Abdul Rahman
A brief description of how to achieve ISO 17025 international accreditation. In this document, you would find how the organizations should react to fulfil the criteria of ISO-17025 and
Lead Auditor Course On FSSC 22000 (Food Safety) - IRCA training in Bangalore,Learn how to audit a food safety management system to ensure its effective operation.
Jim Sylph addresses Ethics Forum participants at the Singapore Accountancy Convention 2014. He the discusses the public's expectations of the profession, recent fraud and regulatory activity, and the how the profession is responding. He also gives an update on the work of the International Ethics Standards Board for Accountants (IESBA) in developing and maintaining the Code of Ethics for Professional Accountants, designed for worldwide application.
How to Perform a Successful Internal Quality AuditGreenlight Guru
You already know internal quality audits are required by both FDA 21 CFR Part 820 and ISO 13485.
You also probably already know they are a big hassle to conduct.
What you might not know is that they are one of the most powerful weapons at your disposal for preventing 483's and observations.
Why?
Because they are one of the most effective and efficient ways to make sure you and your team are always prepared if FDA or NB decided to show up unexpectedly.
So how do you “establish” the right procedures? How do you ensure your auditor is competent and properly qualified? And what do you do if you find non-conformances?
View this presentation by our guest Kyle Rose, President at Rook Quality Systems, where you will find the answers to all those questions and more.
Specifically, you will learn:
- How to conduct an effective internal quality audit based on process identification, sampling and questioning
- How to plan a internal quality audit and develop an audit schedule
- How to find and use competent and qualified auditors
- Why certain auditors shouldn’t audit certain areas
- How to properly report the findings of your internal quality audit
- How to concisely document non-conformances
- How to determine what needs corrective actions and how to follow up on them
ISO17025 Accreditation Procedures and Process Abdul Rahman
A brief description of how to achieve ISO 17025 international accreditation. In this document, you would find how the organizations should react to fulfil the criteria of ISO-17025 and
Lead Auditor Course On FSSC 22000 (Food Safety) - IRCA training in Bangalore,Learn how to audit a food safety management system to ensure its effective operation.
Vinacontrol Group is the first Vietnamese inspection, testing, certification and quality assessment organisation. Established in 1957, Vinacontrol has been a trusted partner of Government Management Agencies, Project Management Units, enterprises and individuals in areas of conformity assessment.
During over 60 years of development, Vinacontrol has made great contribution in ensuring the safety and improving the quality of goods. By that its also contributed to import-export businesses, to domestic quality control of goods and for the whole society.
Vinacontrol network include Head Quaters which is located in Hanoi and 28 branches & units, 7 laboratories and more than 1000 suveyors, appraise experts, analysts. Our solutions are ready to support your business:
- Reduce risk, meet obligation in purchase, payment, delivery, mortgage and insurance procedures.
- Process optimization, ỉmprove quality in each segments of production, transportation, distribution or the whole supply chain
- Building trust, creditbility, doing your business fluently by guaranteeing the quality, safety of products and goods to consumers and partners.
- Comply with the strict regulations of the regulatory body, including local, regional, national and international rules and regulations applied to the production and sale of the goods.
- Ensure quality, safety, health, environment and social responsibility for raw materials, semi-finished products, finished goods throughout the production process and supply chain.
The webinar covers:
• Misconceptions about management reviews
• Evaluating performance of the organization
• How performance reviews affects the bottom line
• How to improvement management ownership of the review process
Presenter:
This webinar was presented by Sheryl Anderson, Managing Director for Quality Systems Solutions & Initiatives (QSSI) and certified trainer for HACCP ISO 9001 & ISO 22000.
Link of the recorded session published on YouTube: https://youtu.be/dGdxT5fyUoc
Design of CCP Monitoring Programs in Food SafetyPECB
The webinar covers:
• Definition of CCP Monitoring;
• Why is Monitoring Needed?
• Main considerations and elements of a well-designed CCP monitoring program.
Presenter:
This webinar was presented by PECB Certified Trainer and Production Manager of “Homefoods Processing & Cannery Ltd,” Samuel Oppong.
Link of the recorded session published on YouTube: https://www.youtube.com/watch?v=qJhF4IWij2A
Auditing plays a major role in offices and companies. It is done to do the required checks. It might be for the operations or it might also be done for the vendors who supply goods.
SQF Code Edition 9: What's New Since 8.1 & Tips for Your Conversion PlanSafetyChain Software
To prepare you for a May 2021 implementation deadline, LeAnn Chuboff from SQFI explains what's changed in SQF Edition 9.0 and how to make your transition smooth.
ISO 9001 - It sets out the criteria for a quality management system and is th...Tushar Sadhye
ISO 9001 - It sets out the criteria for a quality management system and is the only standard in the family that can be certified to (although this is not a requirement).
ISO over one million companies and organizations in over 170 countries implement 9001:2008.
Vinacontrol Group is the first Vietnamese inspection, testing, certification and quality assessment organisation. Established in 1957, Vinacontrol has been a trusted partner of Government Management Agencies, Project Management Units, enterprises and individuals in areas of conformity assessment.
During over 60 years of development, Vinacontrol has made great contribution in ensuring the safety and improving the quality of goods. By that its also contributed to import-export businesses, to domestic quality control of goods and for the whole society.
Vinacontrol network include Head Quaters which is located in Hanoi and 28 branches & units, 7 laboratories and more than 1000 suveyors, appraise experts, analysts. Our solutions are ready to support your business:
- Reduce risk, meet obligation in purchase, payment, delivery, mortgage and insurance procedures.
- Process optimization, ỉmprove quality in each segments of production, transportation, distribution or the whole supply chain
- Building trust, creditbility, doing your business fluently by guaranteeing the quality, safety of products and goods to consumers and partners.
- Comply with the strict regulations of the regulatory body, including local, regional, national and international rules and regulations applied to the production and sale of the goods.
- Ensure quality, safety, health, environment and social responsibility for raw materials, semi-finished products, finished goods throughout the production process and supply chain.
The webinar covers:
• Misconceptions about management reviews
• Evaluating performance of the organization
• How performance reviews affects the bottom line
• How to improvement management ownership of the review process
Presenter:
This webinar was presented by Sheryl Anderson, Managing Director for Quality Systems Solutions & Initiatives (QSSI) and certified trainer for HACCP ISO 9001 & ISO 22000.
Link of the recorded session published on YouTube: https://youtu.be/dGdxT5fyUoc
Design of CCP Monitoring Programs in Food SafetyPECB
The webinar covers:
• Definition of CCP Monitoring;
• Why is Monitoring Needed?
• Main considerations and elements of a well-designed CCP monitoring program.
Presenter:
This webinar was presented by PECB Certified Trainer and Production Manager of “Homefoods Processing & Cannery Ltd,” Samuel Oppong.
Link of the recorded session published on YouTube: https://www.youtube.com/watch?v=qJhF4IWij2A
Auditing plays a major role in offices and companies. It is done to do the required checks. It might be for the operations or it might also be done for the vendors who supply goods.
SQF Code Edition 9: What's New Since 8.1 & Tips for Your Conversion PlanSafetyChain Software
To prepare you for a May 2021 implementation deadline, LeAnn Chuboff from SQFI explains what's changed in SQF Edition 9.0 and how to make your transition smooth.
ISO 9001 - It sets out the criteria for a quality management system and is th...Tushar Sadhye
ISO 9001 - It sets out the criteria for a quality management system and is the only standard in the family that can be certified to (although this is not a requirement).
ISO over one million companies and organizations in over 170 countries implement 9001:2008.
Qualification and Validation have big Weightage in the Regulatory Compliance and GMP. Qualification and Validation only can guarantee about the Product Safety, Integrity, Strength, Purity and Quality assurance.
Week 4:
Quality Management
OPERATIONS MANAGEMENT
1
Outline
Quality definition
Dimension of quality in product and services
Quality assurance
Quality leaders
Cost of quality
Total quality management and tools
Definition of Quality
Quality is a predictable degree of uniformity and dependability, at low cost and suitable to the market (Deming)
Quality is fitness for use (Juran)
Quality is the conformance to requirements (Crosby)
Quality is the (minimum) loss imparted by a product to
society from the time the product is shipped. (Taguchi)
Why Quality
4
Managing quality supports differentiation, low cost, and response strategies
Quality helps firms increase sales and reduce costs
Building a quality organization is a demanding task
4
Ethics and Quality Management
5
Operations managers must deliver healthy, safe, quality products and services
Poor quality risks injuries, lawsuits, recalls, and regulation
Organizations are judged by how they respond to problems
5
Dimensions of Quality for Manufacturing Product
Performance: Product’s primary operating characteristics
Features: Secondary characteristics that supplement the products basic functioning
Reliability: The probability of a product’s surviving over a specified period of time under stated conditions of use
Durability: The amount of use one gets from a product before it physically deteriorates or until replacement is preferable.
Serviceability: The ability to repair a product quickly and easily
Aesthetics: How a product looks, feels, tastes, or smells
Service Quality Attributes
Timeliness: Will a service be performed when promised?
Completeness: Are all items in an order included?
Courtesy: Do front-line employees greet each customer cheerfully and politely.
Consistency: Are services delivered in the same fashion for every customer and every time for the same customers.
Accessibility and convenience: Is the service easy to obtain?
Accuracy: Are the services performed right the first time?
Responsiveness: Can the service personnel response quickly and resolve unexpected problem?
Quality Control
All those operational techniques and activities that are used to fulfill requirements for quality.
The objectives are:
(i) To ensure true expression/correct translation of stated and implied needs of the customers.
(ii) To monitor the process for realization of the product at various stages of its operations and eliminating causes of unsatisfactory performance at all stages of quality loop in order to achieve economic effectiveness.
(iii) Inspection of the product/service package to determine conformance to customer needs.
Quality Assurance
All the planned and systematic activities implemented within the organization for quality management, to provide adequate confidence that a product or service will satisfy given requirements for quality (ISO - International Organization for Standardization).
Quality assurance is a preventive activity an.
Things to remember while upgrading the brakes of your carjennifermiller8137
Upgrading the brakes of your car? Keep these things in mind before doing so. Additionally, start using an OBD 2 GPS tracker so that you never miss a vehicle maintenance appointment. On top of this, a car GPS tracker will also let you master good driving habits that will let you increase the operational life of your car’s brakes.
What Does the Active Steering Malfunction Warning Mean for Your BMWTanner Motors
Discover the reasons why your BMW’s Active Steering malfunction warning might come on. From electrical glitches to mechanical failures and software anomalies, addressing these promptly with professional inspection and maintenance ensures continued safety and performance on the road, maintaining the integrity of your driving experience.
In this presentation, we have discussed a very important feature of BMW X5 cars… the Comfort Access. Things that can significantly limit its functionality. And things that you can try to restore the functionality of such a convenient feature of your vehicle.
Symptoms like intermittent starting and key recognition errors signal potential problems with your Mercedes’ EIS. Use diagnostic steps like error code checks and spare key tests. Professional diagnosis and solutions like EIS replacement ensure safe driving. Consult a qualified technician for accurate diagnosis and repair.
Comprehensive program for Agricultural Finance, the Automotive Sector, and Empowerment . We will define the full scope and provide a detailed two-week plan for identifying strategic partners in each area within Limpopo, including target areas.:
1. Agricultural : Supporting Primary and Secondary Agriculture
• Scope: Provide support solutions to enhance agricultural productivity and sustainability.
• Target Areas: Polokwane, Tzaneen, Thohoyandou, Makhado, and Giyani.
2. Automotive Sector: Partnerships with Mechanics and Panel Beater Shops
• Scope: Develop collaborations with automotive service providers to improve service quality and business operations.
• Target Areas: Polokwane, Lephalale, Mokopane, Phalaborwa, and Bela-Bela.
3. Empowerment : Focusing on Women Empowerment
• Scope: Provide business support support and training to women-owned businesses, promoting economic inclusion.
• Target Areas: Polokwane, Thohoyandou, Musina, Burgersfort, and Louis Trichardt.
We will also prioritize Industrial Economic Zone areas and their priorities.
Sign up on https://profilesmes.online/welcome/
To be eligible:
1. You must have a registered business and operate in Limpopo
2. Generate revenue
3. Sectors : Agriculture ( primary and secondary) and Automative
Women and Youth are encouraged to apply even if you don't fall in those sectors.
"Trans Failsafe Prog" on your BMW X5 indicates potential transmission issues requiring immediate action. This safety feature activates in response to abnormalities like low fluid levels, leaks, faulty sensors, electrical or mechanical failures, and overheating.
5 Warning Signs Your BMW's Intelligent Battery Sensor Needs AttentionBertini's German Motors
IBS monitors and manages your BMW’s battery performance. If it malfunctions, you will have to deal with an array of electrical issues in your vehicle. Recognize warning signs like dimming headlights, frequent battery replacements, and electrical malfunctions to address potential IBS issues promptly.
Why Is Your BMW X3 Hood Not Responding To Release CommandsDart Auto
Experiencing difficulty opening your BMW X3's hood? This guide explores potential issues like mechanical obstruction, hood release mechanism failure, electrical problems, and emergency release malfunctions. Troubleshooting tips include basic checks, clearing obstructions, applying pressure, and using the emergency release.
What Exactly Is The Common Rail Direct Injection System & How Does It WorkMotor Cars International
Learn about Common Rail Direct Injection (CRDi) - the revolutionary technology that has made diesel engines more efficient. Explore its workings, advantages like enhanced fuel efficiency and increased power output, along with drawbacks such as complexity and higher initial cost. Compare CRDi with traditional diesel engines and discover why it's the preferred choice for modern engines.
𝘼𝙣𝙩𝙞𝙦𝙪𝙚 𝙋𝙡𝙖𝙨𝙩𝙞𝙘 𝙏𝙧𝙖𝙙𝙚𝙧𝙨 𝙞𝙨 𝙫𝙚𝙧𝙮 𝙛𝙖𝙢𝙤𝙪𝙨 𝙛𝙤𝙧 𝙢𝙖𝙣𝙪𝙛𝙖𝙘𝙩𝙪𝙧𝙞𝙣𝙜 𝙩𝙝𝙚𝙞𝙧 𝙥𝙧𝙤𝙙𝙪𝙘𝙩𝙨. 𝙒𝙚 𝙝𝙖𝙫𝙚 𝙖𝙡𝙡 𝙩𝙝𝙚 𝙥𝙡𝙖𝙨𝙩𝙞𝙘 𝙜𝙧𝙖𝙣𝙪𝙡𝙚𝙨 𝙪𝙨𝙚𝙙 𝙞𝙣 𝙖𝙪𝙩𝙤𝙢𝙤𝙩𝙞𝙫𝙚 𝙖𝙣𝙙 𝙖𝙪𝙩𝙤 𝙥𝙖𝙧𝙩𝙨 𝙖𝙣𝙙 𝙖𝙡𝙡 𝙩𝙝𝙚 𝙛𝙖𝙢𝙤𝙪𝙨 𝙘𝙤𝙢𝙥𝙖𝙣𝙞𝙚𝙨 𝙗𝙪𝙮 𝙩𝙝𝙚 𝙜𝙧𝙖𝙣𝙪𝙡𝙚𝙨 𝙛𝙧𝙤𝙢 𝙪𝙨.
Over the 10 years, we have gained a strong foothold in the market due to our range's high quality, competitive prices, and time-lined delivery schedules.
Core technology of Hyundai Motor Group's EV platform 'E-GMP'Hyundai Motor Group
What’s the force behind Hyundai Motor Group's EV performance and quality?
Maximized driving performance and quick charging time through high-density battery pack and fast charging technology and applicable to various vehicle types!
Discover more about Hyundai Motor Group’s EV platform ‘E-GMP’!
What Does the PARKTRONIC Inoperative, See Owner's Manual Message Mean for You...Autohaus Service and Sales
Learn what "PARKTRONIC Inoperative, See Owner's Manual" means for your Mercedes-Benz. This message indicates a malfunction in the parking assistance system, potentially due to sensor issues or electrical faults. Prompt attention is crucial to ensure safety and functionality. Follow steps outlined for diagnosis and repair in the owner's manual.
2. MISSION STATEMENT
Mission:
To be a successful supplier with a commitment to employee development,
customer satisfaction, long-term partnerships, continuous improvement,
growth and profitability. VisionTo be the industry leader in providing world
class quality services through strategic partnerships.
Scope:
Quality Assurance Services, Inc. (QAS) provides quality control systems,
servicing all levels of the supplier base with professional resources for on-site
representation, inspection, sorting, rework, and containment certification
meeting ISO 9001:2008 Standards.
3. CUSTOMER ORIENTATION
1) PROCESS NAME :
Inspection of
non-conforming product
3) INPUTS
- Customer specific requirements
- Lot traceability numbers
- Location specific safety requirements
- Production schedules
- Inspection criteria
7) How Effective?
Measurable Objectives)
Key Measurers
- Customer Concerns resulting in PPM
Goal < 2 DECARS Per Quarter (failed containment)
- Site Reporting Errors
Goal 1 or less Per Quarter Per Location
- No Bill Hours
Goal < 10% of Hours Worked not including RI, Training
- Business Growth (Goal 1.1 Million Gross Revenue for 2015)
- Customer Satifaction
- Audits
4) With What?
Resources / Materials / Equipment
- Gages - not supplied by QAS
- Proper lighting
- Office supplies
- PPE
- Laptop
- Cell Phone
- Camera Optional
2) OUTPUTS
( Customer Satisfaction )
Services provided meet all customer and
organizational requirements with respect to:
- Effective QAS Processes
- Quality of work
- Delivery of Product
- Cost of Services Provided
6) How?
Methods / Procedures / Techniques
- Required customer reporting
- QAS Process Flow charts
- Time Study
- Work instructions, Forms, Tags
- Completed production reports
- On the Job training records
5) With Who?
Responsibility / Skills / Training
- Lead inspector
- Inspectors / Sorters
- Client hourly and salaried employees & managers
- Internal and external training
- Knowledge gained from experience
- Inspects suspect material for known non-
conformities
- Maintains lot traceability
- Meets production delivery requirements
- Reworks or repairs components
- Identifies certified material
- Contains non-comforming materials
- Records daily inspection results
- Reports daily inspection results
- Creates work instructions
- Interfaces with all stakeholders
4. CONTROL OF NONCONFORMING MATERIAL
1. Scope
1.1. To describe a uniform method for the review and disposition of material that does not meet customer requirements, facility requirements,
or other established standards.
2. Definitions
2.1. Nonconforming material – is deemed as any material(s) that are not compliant to prevailing standards or customers requirements.
3. Responsibilities
3.1. All employees are responsible for identifying and reporting nonconforming material at the time it is discovered.
3.2. Appropriate personnel are responsible for insuring documentation is completed for all nonconforming material, and that all
nonconforming material is segregated from regular production material.
3.3. The customer/client is responsible for determining the disposition of rejected material.
4. Work instruction
4.1. All unidentified material is classified as nonconforming and must be rejected.
4.2. Nonconforming material (i.e containers, parts) must be identified with a completed reject sticker. Appropriate personnel shall complete
the reject sticker.
4.3 The reject tag information must be recorded in the production report.
4.4 Following the completion of the re-operation (i.e. re-inspection and sort, rework, etc.), the personnel performing the re-operation applies
a blue QAS sticker with date and initial, if it was already inspected once and has another QAS sticker.
4.5 The Site Supervisor will communicate to the customer the status of nonconforming product if shipped to the customer.
4.6 The customer may request the non-conforming product be used in production under some circumstances. A deviation or equivalent
authorization must be signed by the customer to return rejected material into production.
5. Customer Report/Complaints
5.1. Nonconforming material returned by the customer will immediately be placed in the containment area.
5. PROCESS OVERVIEW
Customer
Requirements
Inspection / Sorting
Not Defined
RequiresValidation
Customer Liaison
Request
for
Quote
Measure
Define
Analyze
Improve
Control
Defined
Meets
Intent
Planning
Validated
by Client
Receive
Materials
Inspect
Product
Contain
Defective
Return
Good
Material
Customer
Request
for
Quote
Meets
Intent Client/LiaisonValidat Execute Report Customer
6. PREVENTIVE ACTION
Scope
This procedure addresses review of opportunities for Preventive Actions, implementation and verification of Preventive Actions.
Definitions
8D– Eight Discipline root cause analysis
Preventive Action - a change implemented to address a weakness in a management system that is not yet responsible for causing a non-conformance
Responsibilities
All employees may report opportunities for Preventive Actions (e.g. Employee Suggestions)
Management review team members should bring opportunities for Preventive Actions to the monthly/quarterly/ or annual meetings for discussion and review by the team
The Director of Quality is responsible for reviewing the effectiveness of Preventive Actions on a regular basis
The Site Supervisor or Site Operations Manager may implement Preventive Actions suggested by employees that affect process or safety concerns, without prior review of the management team with review and approval from the Director of Qu
Work instruction
A report of Preventive Actions taken will be done utilizing the Management Review process.
When opportunities for Preventive Actions are discovered, the Team will assign responsibilities for the completion of the Preventive Action to the appropriate person.
Three major mechanisms of preventive actions should be considered:
Preventing mistakes (defects) from occurring (MISTAKE PROOFING or POKE-YOKE)
Mistake proofing methodologies may be applied to all Corrective Actions to a degree that they will address quality systems and product/process problems encountered and prevent problems associated with risk factors inherent in the pro
product. Documentation of mistake proofing will be included in the 8-D Corrective Action
Where mistakes cannot be poke yoke, a method of detecting them early to prevent them from being passed down the supply chain should be utilized
Where mistakes reoccur, measures to ensure that production automatically stops until the process can be corrected should be implemented to prevent the production of more defects.
Techniques to implement effective prevention may include:
Standards and standard operating procedures.
Use of clear documentation and checklists prior to initiation of work.
Training—for both correct processing and for inspection, detection, and appropriate response.
Control of information to prevent input of defective material or incorrect information.
Poke-yoke mechanisms or procedures for mistake proofing.
Planning prior to initiating a project, and working to plan.
Discipline to insure the application of the above as appropriate.
Records of the Preventive Action Review will be documented in the management review meeting minutes.
7. INSPECTION OF
NON-CONFORMING PRODUCT
1) PROCESS NAME :
Inspection of
non-conforming product
3) INPUTS
- Customer specific requirements
- Lot traceability numbers
- Location specific safety requirements
- Production schedules
- Inspection criteria
7) How Effective?
Measurable Objectives)
Key Measurers
- Customer Concerns resulting in PPM
Goal < 2 DECARS Per Quarter (failed containment)
- Site Reporting Errors
Goal 1 or less Per Quarter Per Location
- No Bill Hours
Goal < 10% of Hours Worked not including RI, Training
- Business Growth (Goal 1.1 Million Gross Revenue for 2015)
- Customer Satifaction
- Audits
4) With What?
Resources / Materials / Equipment
- Gages - not supplied by QAS
- Proper lighting
- Office supplies
- PPE
- Laptop
- Cell Phone
- Camera Optional
2) OUTPUTS
( Customer Satisfaction )
Services provided meet all customer and
organizational requirements with respect to:
- Effective QAS Processes
- Quality of work
- Delivery of Product
- Cost of Services Provided
6) How?
Methods / Procedures / Techniques
- Required customer reporting
- QAS Process Flow charts
- Time Study
- Work instructions, Forms, Tags
- Completed production reports
- On the Job training records
5) With Who?
Responsibility / Skills / Training
- Lead inspector
- Inspectors / Sorters
- Client hourly and salaried employees & managers
- Internal and external training
- Knowledge gained from experience
- Inspects suspect material for known non-
conformities
- Maintains lot traceability
- Meets production delivery requirements
- Reworks or repairs components
- Identifies certified material
- Contains non-comforming materials
- Records daily inspection results
- Reports daily inspection results
- Creates work instructions
- Interfaces with all stakeholders
8. CLIENTS•AGC Automotive
•Arvin Meritor
•Dura Automotive
•Faurecia
•Ficosa
•Ford Motor Co.
•Guardian
•Jing Mei
•Johnson Controls
•O & KTechnologies
•Kongsberg
•Magna Mirrors
•Rochester Metals
•LairdTechnologies
•Perfect Equipment
•Baolong
•Continental
•Cooper Standard
•Decostar Industries
•Douglas Corp.
•Faist Chemtec
•Federal Mogul
•Flex-N-Gate
•Grote Industries
•Harada Industries
•Hi-Lex Corporation
•ITW Deltar
•Kam Plastics
•Magna Composites
•S Group
•Sanyo Automotive
•Trelleborg
•WKW Automotive
•Zeledyne
FORD MOTOR CO.
Michigan Assembly, Wayne Assembly, Dearborn Truck, Louisville Assembly, Kentucky Truck, Kansas City Assembly, Auto Alliance, Oakville Assembly,
Twin Cities Assembly, St. Thomas Assembly, Chicago Assembly, Ohio Truck, and Hermosillio, Mexico
CHRYSLER
Toledo Jeep (North/South), Jefferson North, Windsor Assembly, St. Louis (North/South), Warren Truck, Brampton, CN, Belvidere, and Chrysler Mexico
GM
Orion Assembly, Arlington, TX, Flint, MI and Ft. Wayne Assembly, Lansing, Fairfax, Oshawa, and Cami, CN, GM of Mexico
HONDA
Marysville, OH and Lincoln, AL
KIA
West Point, GA
MERCEDES
Tuscaloosa, AL
BMW
Spartanburg, SC
MOTOR COACH INDUSTRIES
Winnipeg, MB, Canada
GILLIG CORP.
San Francisco, CA
TOYOTA
Cambridge, Canada, Woodstock, Canada, and San Antonio, TX
NASHVILLE GLASS
Nashville, TN
VOLKSWAGEN
Chattanooga, TN
9. THE SOUTH REGIONTEAM
Lenn Coffey
Regional Site Operations Manager
Cell 256-504-9117
l.coffey@qaservicesinc.com
http://qaservicesinc.com/
LidiaTurner
Regional Business Manager
Cell 256-282-8055
Office 205-763-1514
Fax 205-763-1521
l.turner@qaservicesinc.com
http://qaservicesinc.com/