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QRQC

Quick Response Quality Control


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What is QRQC?

QUICK RESPONSE QUALITY CONTROL

A MANAGEMENT
attitude to
solve ANY KIND OF
PROBLEM
-REAL PLACE-
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Why QRQC?

• Cost of Goods Sold


• Cost of Quality
• Scrap
• Line Interruption
• Quick Response to Customers
• Quality
• Inventory Turns
• Throughput
4

How to deploy? Who should do it?


To do QRQC, we need COACHES / LEADERS
Standardize reaction to significant External/Internal Quality
failures.
Instil problem solving discipline through use of a standard.
Promotes communication and sharing of knowledge through
shop floor QRQC activities.
Utilizes a visual method of displaying important information to
drive closure .

Daily on-the-job coaching to support the culture by


* Plant Manager
* Department Managers (HR, Logistic, Production, Quality,
Controlling, Maintenance, Development …)

- Learn from shop floor


- Give positive motivation, not make
people afraid
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Understand QRQC?
THE 3 REALS

Real place: Where and when it happens

Real parts: What is really the defect and


compare to good

Reality: Expressed with DATA and


compared to standard
6

Understand QRQC?

LOGICAL THINKING
What is the problem?

What is the root cause?

What is the counter measure?

What can I commit for the future?

At the end, the story is easy


to understand.
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The 6 Key Principles of QRQC


1. Going to the real place 1. REAL PLACE
(Workplace)
2. Compare real parts 2. REAL PARTS
- a BAD part,
- a GOOD part,
- produced at the SAME TIME
3. Speaking with data 3. REAL DATA
4. Have a quick reaction, react fast 4. QUICK RESPONSE
5. Using logical thinking to find 5. LOGICAL THINKING
root causes
6. With on the job coaching by 6. COACHING
management
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QRQC Tools and Organization


TO SUPPORT QRQC on the shop floor

A simple piece of paper on a board support visible in the


real workplace

All support functions are involved


in problem solving lead by the
owner

Plant QRQC
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Methodology

How to do
PLANT
QRQC
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How to do PLANT QRQC?


Who attends?
Production Manager drives the meeting with Quality representative.
Supervisors, Maintenance.
Others as required: SQE, Engineering, Logistics…
Plant Manager & Quality Manager attend at least once a week.

What ?
Review impact of yesterday’s actions.
Review the customer complaints (f.i. finding root causes, corrective
actions) .
Review 3 most important problems of the production line (Choice made
by Production Manager, importance based on criticality, complexity,
recurrence and quantity of parts)
Assign actions.

When?
SET TIME, Every day

How?
Using QRQC boards (“Parts in hand”)
PLANT QRQC- 8D discipline

Customer issues
Re-occurring or more complex
problems.
Internal issues , high severity ( 8 -10)
Step 1 Form the team & Define milestones
review

Step 2 : Description of the problem

Step 3 : Temporary contrameasures

Step 4 – Possible Cause and Root Cause

Step 5 - Corrective Actions & Step 6 - Verify


Results

Step 7 – Prevent Recurrence

Step 8 – Congratulate the team


Line QRQC

Line issues(severity 1 -7)


Step 1 Form the team & Define milestones
review

Step 2 : Description of the problem

Step 3 : Temporary contrameasures

Step 4 – Possible Cause and Root Cause

Step 5 - Corrective Actions & Step 6 - Verify


Results

Step 7 – OK & NOK samples

Step 8 – Congratulate the team


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Plant QRQC

Step
D1 Form the
team & Define
milestones
review
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QRQC

Step
D2 Problem
Description
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5Ws,2Hs

 Purpose
 Describethe situation as detailed as you can, understand
the problem.

 Method
 Adopt an interrogative attitude (abandon preconceived
ideas). Describe what you need to know to start!

WHAT WHO WHERE WHEN WHY


(is it a problem)
HOW was the HOW MUCH
problem found?
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Is / Is not and Differences


 Purpose
 Ask the questions – “not only why under some circumstances the problem
occurs, but also why, under other circumstances, the problem does not
occur”. And from there, identify differences.

 Method
 What?
 Why this part / this reference and not that one?... Difference?
 Who?
 Why Mr. X and not Mrs. Y?... Difference?
 Where?
 Why here and not there?
 Why this process and not that one?... Difference?
 When?
 Why today and not yesterday?... Difference?
 How?
 Why this way and not that ways ex: detection?... Difference?
 How many?
 Why more with A than with B?... Difference?
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Quotation

IfI had 100 minutes to


solve a problem on which
my life depended, I would
spend 75 minutes to
understand it, 15 minutes
to find solutions, and 10
minutes to implement
them…..

…. Albert EINSTEIN
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Step D2 allowed us to…

KEY POINTS OF THE STEP BASICS TO BE RESPECTED


DURING THIS STEP

Define the problem in a REAL WORKPLACE


factual way with the help of
5Ws2Hs REAL PARTS
Define likely factors using the REAL DATA
tool IS-IS NOT –DIFFERENCE
Implement problem follow-up
indicators
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COMPLETION OF QRQC FORM - ( EXAMPLE)


5W and 2Hs
D2 Problem description

DETECTION PLACE : CREATION PLACE :


What was the problem ?

Part with missing hanger


Why was it a problem ?

It is impossible to assemble the part in the car


When was the problem found ? When produced ?

10/02/2009 first shift 05/02/09, 1st shift


Who found the problem ? Who inspected the parts ?

Evandro Rodrigues (GMB) Operator in 1st shift (Marcus)


Where was the problem found ? Where was the problem created ?

Assembly Line Gmdo Brasil (CQPC) At the manual welding station for the hangers
How was it found ? How it was created ?

During the assembly of the part Operator only welded 3 / 4 hangers


How many where found ? How many suspect parts ?
1 part 920 parts at customer, 324 parts in KSS Plant
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COMPLETION OF QRQC FORM - ( EXAMPLE)


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Process Mapping

 What is its purpose?

- Formalise the real progression of the process,


 - Help share the same vision of the process,
 - Identify all inputs/outputs data of the process.

 What method?
 Review all elements that constitute the process
(manufacturing equipments, various flows).

 The group must review all the phases of the process.


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Step D2 allowed us to…

KEY POINTS OF THE STEP BASICS TO BE RESPECTED


DURING THIS STEP

Thanks to Process Mapping: LOGICAL THINKING


Understand the manufacturing
process
Identify similar products and
processes risks
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QRQC

Step
D3
Containment
Actions
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Containment Actions
 Goals:
 Defineactions to be taken within 24 hours in order to
protect the customer.

 Method:
 Implement these actions and validate their efficiency.
 In a few hours maximum, ensure that no non-conforming
part persists between you and your customer, at your
customer, or in the market.
 Deploy those actions on all similar products / processes
listed during Step D2.

 Tools:
 Actions plan (PDCA)
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Action Plans

PDCA

MODIFY DESCRIBE
GENERALISE ANALYSE
STANDARDISE FIND

Act Plan

Check Do
EXECUTE
MESURE THE EFFICIENCY
OF THE RESULTS
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Step D3 allowed us to…

KEY POINTS OF THE STAGE BASICS TO BE RESPECTED


DURING THIS STAGE

Define actions plan to protect QUICK REACTION


the customer with PDCA
Examples:
Systematic sorting of existing
stocks
Implement 100 % check
during production phase
(Quality Wall)
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COMPLETION OF QRQC FORM - ( EXAMPLE)

Target date > 11-02-09


Action: Pilot Dead line Check by shift / Sorting results
Visual inspection of 100% of stock at customer Fábio start Check realized through contracted company
Somenci 10/02/09 ACS: 920 peças checked 0 NOK parts found
end
14/02/09
12:00hs
100% visual inspection of Faurecia stock Roberto 11/02/09 1º Shift: 124 parts checked – 0 NOK found
(finished goods in safety stock, TPA) Souza 14:00hs 2º Shift: 200 parts checked – 0 NOK found

Emission of Quality Alert for the Production Roberto 10/02/09 Quality Alert Nº 02/09 emitted 10/02/09 and
line Souza 16:30hs received (signed) by both shifts’ operators

Inclusion of production process the visual Willian Bozzi 11/02/09 Marking of rack specified in Quality Alert
check of 4 hangers and marking of each 09:00hs 002/09 started from 09:00 hrs.
hanger with industrial marker by operator.
Identification of the racks with paper “100% Telephone Contact with Quality representative
inspected for hanger” at GM plant to confirm reception of first lot of
controlled parts by 11/02/09 (18:00).

Transfer of claimed part from customer for Fábio 11/02/09 Part available in Pinda plant by 17:00 hrs
root cause analysis. Somenci 17:00 revealed that it was produced in 1st shift on
Feb 5th by operator Marcus
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QRQC

Step
D4
Possible
causes(Root cause)
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Possible causes (Root cause)


 Method:
 1- Analyze 5 Whys for escape
 2- Analyze 5 Whys for “How the part was made”?
 3- Analyze 5 Whys for “Why it was not prevented”?
 4- Define and implement associated actions' plan
 5- Validate likely causes

Tools:
 1- Brainstorming , Ishikawa or 6M.
 2- Weighted Vote
 3- Action plan
 4- 5 Why's, Gage R&R, Action plan
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QRQC

Step
D5
Corrective
Actions
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Corrective Actions
 Goals:

 Define actions to be taken in order to eradicate problem


causes
 Follow-up of action implementation
 Be careful that the implementation of the actions does not
cause other problems
 Identified corrective actions that must be implemented

 Tools:
Brainstorming
Action Plan (PDCA)
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COMPLETION OF QRQC FORM - ( EXAMPLE)

Target date > 10-04-09


Action Responsible Deadline Check by shift
Modify the concept of the PY in a sense Willian Bozzi 10/03/09 12-03-09 Shift 1º (OK) Shift 2º (OK)
that the equipment will not only
detect the presence of the hangers
but also:
a) the amount of welding seams and
b) the time spent for each seam.

The equipment will release the part once


the correct amount of welding
seams has been realised with the
standard time for each seam.
Update Work instruction and Instruction Willian Bozzi 11/03/09 12-03-09 Shift 1º (OK) Shift 2º (OK)
for PY

Update the training of the Operators in Willian Bozzi 12/03/09 13-03-09 Shift 1º (OK) Shift 2º (OK)
line with the adaptations of the process.

Realize Lessons Learned Sheet Daniel Ferrari 18-03-09 OK Done 17-03-09


Shift 1º (OK) Shift 2º (OK)
Ask Division Management to include P- Roberto Carlos / 18.03.09 Training realized 26.02.2009 by SGS
FMEA training for key individuals of Willian Scopinho
Pinda Plant
Assure strict respect of Work Package Roberto Carlos 28.02.09 Realized since Phase 3 PSA T3 Program
“Lessons Learned Revsion” for each (Mar 10th 2009)
respective Program Phase
Assure participation of key persons in P- Roberto Carlos From Done 11.03.2009
FMEA creation (Prod, ME, Q, D&D, Purch.) 18.03.09
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QRQC

Step
D6 Verification/ Action
Plan effectiveness
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Verification /Action Plan Effectiveness

 Goals:

 Validate effectiveness of the actions taken,

 Validateproblem control during at least one month before


closing it in step D8

 Verify implemented actions did not create new problems

 Tools:
Tracking Chart
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Tracking Chart

 What is its use?


 Allows
a follow-up of the evolution of the chosen indicator
and the efficiency of actions taken.

 What method?

1. Follow indicator's evolution (phase D1) .


2. List the various actions to be taken and planned
3. Note down the date of real implementation
4. Validate each action's effectiveness.
37

Step D6 allow us to…

KEY POINTS OF THE STEP BASICS TO BE RESPECTED


DURING THIS STEP

Verify effectiveness of the REAL DATA


actions taken to remove
containment measures
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QRQC

Stage
D7
Prevention
39

Step D7 allow us to…

KEY POINTS OF THE STEP BASICS TO BE RESPECTED


DURING THIS STEP

Who needs to be informed of REAL DATA


the solution?
What did you change that will
prevent reoccurrence of the Root
Cause?
Was the D/P FMEA updated ?
Was the Control plan updated?
Was the corrective Actions
implemented on similar
products?
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QRQC

Step
D8 Congratulate
the team
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Step D8 allow us to…

KEY POINTS OF THE STEP BASICS TO BE RESPECTED


DURING THIS STEP
Verify goals have been achieved
ON JOB COACHING
Inform the personnel
Update workstations‘
documentation
Update FMEA’s and Control
Plans
Modify design standards
Obtain final validation of the
plant Management for the QRQC
closure
42

COMPLETION OF QRQC FORM - ( EXAMPLE)

Target date > 10-04-09

Action Responsible Date

Objectives met Wiliian Bozzi 10-03-09


Done

Operators informed Willian Bozzi 12-03-09


Done

Workstation docs. Daniel Ferrari 11-03-09


Updated Done

FMEA updated Daniel Ferrari 11-03-09


Done

Control plan updated Daniel Ferrari 11-03-09


Done

Design standards NA -----


updated
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Daily management of QRQC

QRQC
Management
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QRQC - Development conditions for daily
meetings?
Who attends?
Production manager drives the meeting with Quality manager.
Inter-departmental team established at the beginning of analyse .

What?
Review the analysis according with schedule.
Check the action which were schedule to be completed untill revision.
Evidence gathering and archiving.

When?
SET TIME, Every day.

How long ?
30 minutes

Where ?
At Plant QRQC area.
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Conclusion - Key messages

Eyes and legs to see quickly reality.

Quick Response / Daily meeting / Logical thinking.

3 Reals: Real part / Real data / Real Place.

Compare good parts / bad parts and the standard .

Manager task: on job training and task assignment.

Visual display area.

Lessons learned to share and build standards for future.


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The leader daily obsession

▫ Did you IMPROVE something today?

▫ Did you LEARN something today?

▫ Did you TEACH something today?

▫ Did you CONGRATULATE somebody today?

Don’t forget:
Your hands must be „dirty“ when you do QRQC
correctly !!
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Good and bad practices


TOP-DOWN Support Managers not involved, QRQC
Enforcement of 3 ‘Reals’, driven by Quality.
commitments met Bla - bla. Opinions. No part. No
Daily reviews, at set time, listening to operators.
with set attendance.
Deadlines not committed.
Punctuality.
Managers assigning tasks ‘No time today’. Deadlines
Tasks reported in reviews, drifting
with data. Reviews used for discussion /
Logical thinking . brainstorming.
Challenged, step by step No real report, data missing.
approach.
No challenge. Rush to actions
Managers escalating
roadblocks. without root causes proven.
Coaching as a daily duty No escalation. Problems left
‘What did you learn today?’ reoccurring
Did not achieve learning
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Typical Behaviours observed Key Point / Recommendations

'Normally…', 'To me…', 'I think…', Real Data -> Correct your team upon hearing such statements!!!
'Probably…' , 'I am quite sure -> 'I am not supposed to trust what you say'. Demand evidence of
that…', 'This occurs quite often'; 'It what people say. Go yourself to the real place to check.
should work now…'

Team rushing to actions Logical Thinking -> Get reports structured as:
1. What is the problem?
2. What are root causes?...and countermeasures?
3. How do you prevent reoccurrence?

. Wait for reviews to start thinking Quick Response -> Check deadlines.
about problem
. Let deadlines drift, allow long
response time

'We are so busy we have no time for On Job Coaching -> Doing QRQC properly will save you time and avoid
QRQC' you running inefficiently in all directions

No lessons learned Logical Thinking -> 'Did you understand why the problem can happen ?
What did you do to capitalize ?' Promote Lesson Learned Sheet

'No support from Division, Management -> The design office is one of your suppliers. You have a
engineering…' role to play to escalate problems.
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CONGRATULATE
THE TEAM!!!
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Next Steps
• Define “Red Bin” Defect codes with Severity
Ranking
• Develop Implementation Pilot Program
▫ Training Module
▫ Who will be trained (Line Leader, Supervisor,
Plant Management)
▫ Roles and responsibilities Defined
• Kick-off of the Pilot Program
• Evaluate Pilot Program Results

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