Quality Control training

Slides:



Advertisements
Similar presentations
ISO 9000 Quality Standards ISO 9000 describes quality assurance elements in generic terms that can be applied to any business. It treats an enterprise.
Advertisements

ISO 9001:2000 Documentation Requirements
Transition from Q1- 8th to Q1- 9th edition
Ensuring Better Services and Fair Value “Introduction and roadmap to implementation of ISO in Zambia’s water utilities” Kasenga Hara March 2015.
Chapter 9A Process Capability and Statistical Quality Control
 Contracts  Subcontracting  Suppliers  Complaints  Corrective and preventive actions (CAPA)  Internal audits  Management reviews Management requirements.
ISO 9001 : 2000.
EPSON STAMPING ISO REV 1 2/10/2000.
Where does Failure Mode and Effects Analysis (FMEA) come from?  Developed by the Aerospace industry in the1960s  Spread to the Automotive industry 
ISO Culture SHOQ Quiz 1. This program must be run in MS PowerPoint and requires sound. 2. Click “View” and then “Slide Show”. 3. Click “Continue”
Supplier SQM Participation. 2 | MDT Confidential What is SQM? Stands for Supplier Quality Managment –Formally referred to as SPACE and SPICE Is a system.
SAE AS9100 Quality Systems - Aerospace Model for Quality Assurance
The ISO 9002 Quality Assurance Management System
Quality Management System
Statistical Process Control
Chapter 11 Quality Control.
Quality Assurance/Quality Control Policy
D. Keane June Internal Quality Audits (4.14) -ISO Requirements for Internal Audits -The Audit Process -Templates for Meeting Requirements.
RC14001 ® Update GPCA Responsible Care Committee September 23, 2013.
Prepared by Long Island Quality Associates, Inc. ISO 9001:2000 Documentation Requirements Based on ISO/TC 176/SC 2 March 2001.
ISO 9000 Certification ISO 9001 and ISO
QMS ISO 9001:2008 Introduction to QMS 9001:2008 and system auditing.
5.2 Personnel Use competent staff Supervise as necessary
© 2009 Michigan State University licensed under CC-BY-SA, original at Corrective Action.
NVLAP Overview and Accreditation Process March 2006.
ISO/IEC A review of the new standard for laboratory accreditation
QUALITY MANAGEMENT SYSTEM ACCORDING TO ISO
Creating Lasting Change for Your Business ISO 9001:2000 Management System Overview.
Ships in Service Training Material A-M CHAUVEL QMS Terms & Definitions 2009.
Introduction to ISO New and modified requirements.
ISO 9000 and Public Awareness and Information Session 22 February 2006 Owen Glave, MBA-TQM.
Software Quality Assurance Lecture 4. Lecture Outline ISO ISO 9000 Series of Standards ISO 9001: 2000 Overview ISO 9001: 2008 ISO 9003: 2004 Overview.
WHY CONFORMITY ASSESSMENT?. What is conformity assessment?  Conformity assessment is the name given to processes that are used to demonstrate that a.
Introduction to ISO 9001:2000.
ISO 9000 & TOTAL QUALITY ISO 9000 refers to a group of quality assurance standards established by the International Organization for Standardization.This.
Lecture #9 Project Quality Management Quality Processes- Quality Assurance and Quality Control Ghazala Amin.
Company Confidential Improvement Opportunities for Audit Reporting Tony Marino and Rick Downs July 19-20, 2012 Registration Management Committee RMC Workshop.
Quality Control Project Management Unit Credit Value : 4 Essential
4.3 Document control 4.4 Review of requests, tenders and contracts
Purpose of audit is to provide assurance that: Procedures for attaining quality are such that, if followed, the intended quality will be obtained.
Project quality management. Introduction Project quality management includes the process required to ensure that the project satisfies the needs for which.
International Aerospace Quality Group The Initiatives of the International Aerospace Quality Group (IAQG) Steve Shepherd ~ European Sector Leader.
1 Slides used in class may be different from slides in student pack Technical Note 8 Process Capability and Statistical Quality Control  Process Variation.
The Second Annual Medical Device Regulatory, Reimbursement and Compliance Congress Presented by J. Glenn George Thursday, March 29, 2007 Day II – Track.
19-Feb-16 “"Dana Confidential Information - Those having access to this work may not copy it, use it or disclose the information contained within this.
Visit us at E mail: Tele:
DOCUMENTATION ISO/IEC 17025:2005 Documentation.
Technology Services – National Institute of Standards and Technology Conformity Assessment ANSI-HSSP Workshop Emergency Communications December 2, 2004.
Q uality C oncepts. WHAT IS QUALITY ? ‘Quality’ is now a familiar word.  When most people talk about the quality of an object, or service, they are normally.
November 6, 2013 Purchasing Controls & Supplier Quality Best Practices Beyond Compliance for the Medical Device Industry AdvaMed 2013 Bernie Liebler Technology.
Quality Management: Mutually beneficial supplier relationships.
UNDERSTANDING ISO 9001:2008.
QUALITY CONTROL FOR NFI
LESSON 2 Statistical Sampling
Project Quality Management
Project Management PTM721S
ISO/IEC
SEVERITY & PRIORITY RELATIONSHIP
Fundamentals of ISO.
Achieving ISO Compliance
ISO 9001 Awareness Training.
Managing Supplier Quality
UNDERSTANDING FOR STANDARD
Emulsion Task Force Meeting
How to conduct Effective Stage-1 Audit
Chapter 11 Quality Control.
Chapter # 1 Overview of Software Quality Assurance
ISO 9001:2000 Management System Overview
Nonconformity Writing
Quality Systems ISO 9000 Series QS-9000 TE-9000 AS9000
Presentation transcript:

Quality Control training Stéphane Huot-Marchand; 2017

Summary Training program Quality product, Quality Control and Quality Management Quality Control on Essential Household Items Determination of acceptability V) QC key points and continuous improvement

Quality Control training Program Day 1 Day 2 Day 3 Day 4 Day 5 8h00 10h30 Introduction to QC (Meeting room) Practical training on tarpaulins QC (Warehouse + Meeting room) Practical training on jerry cans QC Practical training on sleeping mats QC Practical training on Family tents QC Break 10h45 12h00 Installation of stand, table and drop test bracket. (Warehouse) Practical training on sleeping mats QC (Warehouse + Meeting room) Lunch 13h00 15h00 Practical training on blankets QC Practical training on Oxfam buckets QC Practical training on mosquito nets QC Practical training on kitchen sets QC Wrap up / Training Evaluation 15h15 17h00

Summary Training program Quality product, Quality Control and Quality Management

Quality product : The degree in which customer requirements are met. What? Quality product : The degree in which customer requirements are met. Not looking for over-quality but for the right quality requested. For instance if you need handkerchiefs ....Looking for the right type for the right use. Right quality when sneezing or coughing Right quality when going to cocktail

Quality Control : Consists of activities of detection and measurement of the variability in the characteristics of product. → QC insures we are getting what we pay for. QC insures no over-invoicing from suppliers. It includes corrective actions. Without requirements (specifications) no accurate Quality Control. Purchasing a white car! QC based on which spec? (colour only!) How? City car 4WD

Quality Management : Consists not only on product quality (and goods testing) but also on the means to achieve it. It includes establishment of Quality policy and objectives; Documentation management; Quality, Social and Environmental manufacturer’s audit and assessment; QC and procurement processes improvement. Why?

Summary Training program Quality product, Quality Control and Quality Management Quality Control on Essential Household Items

EHI Tarpaulins Blankets Kitchen sets Buckets Jerry cans Mosquito nets Sleeping mats Family tents

B- Comments and pictures QC methodology: Quality Control documents (Excel file) based on specification (one specific document for each EHI, made on the same design). A- Summary report B- Comments and pictures C- Data recording D- Instructions E- Formulas 10

QC methodology: Quality Control documents (Excel file) based on specification one specific document for each EHI, made on the same design). QC area in the warehouse , equipment/tools for inspection needs (table, stand, thickness gauge, weighing machine…) + identification and calibration process. https://prezi.com/e0r-d8qfpps3/procedure-for-assembling-the-icrc-quality-control-table/ https://prezi.com/3fqhl1cmqdig/procedure-for-assembling-the-icrc-quality-control-stand-and-bracket/ 11

QC methodology: Quality Control documents (Excel file) based on specification (one specific document for each EHI, made on the same design). QC area in the warehouse , equipment/tools for inspection needs (table, stand, thickness gauge, weighing machine …)….and calibration process. Staff training (controllers should be trained on QC protocol) 14

QC methodology: Quality Control documents (Excel file) based on specification (one specific document for each EHI, made on the same design). QC area in the warehouse , equipment/tools for inspection needs (table, stand, thickness gauge, weighing machine …)….and calibration process. Staff training (controllers should be trained on QC protocol) Inspection 15

16

Summary Training program Quality product, Quality Control and Quality Management Quality Control on Essential Household Items Determination of acceptability

Zero nonconformity ? (space shuttle Challenger) "There is no such thing as zero nonconformity“ (space shuttle Challenger) Thus, it is important to know what proportion of nonconformities is tolerated. If you are in the aviation business, any defective part might cause a disaster, so your tolerance will be very, very low. (e.g. for some parameters controlled Acceptance Quality Limit = 0.00001% of nonconformity → high cost items) But you will have to accept a higher percentage of nonconformities if you source products in low cost countries. S.Huot-Marchand AQL

AQL and rejection number Acceptance Quality Limit. The AQL is the quality level that is the worst tolerable in average (based on sampling and probability) AQL 0 means no nonconformity on the parameter inspected is accepted. AQL 4.0 means max of 4.0% of nonconforming products accepted on the parameter inspected in average. AQL 6.5 means max of 6.5% of nonconforming products accepted on the parameter inspected in average. Rejection Number. The rejection number is the minimum number of nonconforming products in the sample that will cause rejection of the lot.

Nonconformity definitions Critical nonconformity. Any discrepancy which might harm a user or makes it impossible to use the product properly is considered to be critical. (AQL=0) Major nonconformity. Any discrepancy which makes the usage of the product less efficient than expected is considered to be major. (AQL=4.0) Minor nonconformity. Any discrepancy which does not have an influence on the performance of the product is considered to be minor. (AQL=6.5)

Sampling plan made according to ISO standard 2859

Example

- The Acceptance Quality Limit is defined by the Quality Manager together with buyers and technical team, and then written in call for tenders, purchasing contracts and QC doc. The number maxi of accepted nonconformity (Rejection number) is automatically determined by the Excel file for each parameter (this is automatically adjusted according to the sample size → Formulas sheet) - For each parameter, the Excel doc shows if it is conform (accepted) or nonconforming (rejected) using the data written by the controller in data recording sheet.

The summary report shows the Pareto of non-conformities If one parameter is nonconforming, it is indicated in red in the summary report several corrective actions are proposed (drop-down list) 26

Summary Training program Quality product, Quality Control and Quality Management Quality Control on Essential Household Items Determination of acceptability V) QC key points and continuous improvement

QC insures we are getting what we pay for. QC implementation (4 steps): documents, equipment, training, inspection. QC process does not slow down the supply chain (by using appropriate inspection level). QC is based on a physical control by internal controllers and/or laboratories (UV test…). QC inspection reports must be of high quality (suppliers use any QC report mistake to gainsay the findings). 28

QC is one of the last steps of the procurement process, which is the detection of non-conformities (Ref procurement process) Efficient procurement process requires good cooperation between Sourcing manager, Buyers and Quality teams. Vertical integration (working with known manufacturers ….and not traders) decreases the number of quality issues, allows a better management of corrective actions and nonconforming items found by QC.

Some nonconformities found by QC on tarpaulins and kitchen sets

Tarpaulins manufacturer visit further to QC findings Kitchen sets manufacturer visit further to QC findings No more nipple on this bearing

Example of corrective action taken by procurement Unit: Purchasing from manufacturers showing evidences of process performance control.

 QC outputs are useful for procurement process improvement. QC findings + suppliers audits help to evaluate suppliers performance. Comparing apple to apple Documentation QC is part of Quality Management (process approach) Measure processes performance. Implement actions of improvement.  Provide assurance to customers about quality and capability.   Internal customers Beneficiaries Donors

Thank you In case of any question, comment, suggestion do not hesitate to address a message to shuotmarchand@icrc.org