Practical Way to raise NCR's in an Assembly Workshop

Q

QAMTY

Hi everybody

Could you share a practical way to raise ncr´s in an assembly workshop

ISO 9001 2008, states that in order for the bad products do not arrive at client, an NCR should be raised, from then a disposition is needed, scrap, to repair, to be accepted for the client, etc.

But is not recommended to raise an NCR for everything, if it is a minor NC, maybe is not necessary to raise the ncr, but if it is a big or medium problem, for sure it is needed to raise the NCR.

From that a CAR is expected.

The point is how to put this in practice?, what criteria to follow in order to make this process easy and practical, that really adds value.

It may be, if the bad product is 3%, raise the RNc, other criteria if the cost of raw material falls in certain amount $$, raise the RNC, but doing it using such criteria is not so simple to be applied in all products.
Raisings NCRs for everything,additionally to perform CA´s, I think is wasting time and efforts.

What citeria do you use/follow to raise NCRS´s in your business?

Please share your comments.
Thanks
 
D

DRAMMAN

Well, first off do not focus on using ISO9001:2008 since it is obsolete. Go read ISO9001:2015.

I assume you are referring to documenting a Non-Conformance Report. ISO does not specifically state you must do this. Although you do need to prevent non-conformances from reaching customers. In a practical sense you are likely not going to record everything in an assembly process. As you stated you will not want to record every single instance of an operator experiencing a NC. Simple things will be fixed on the fly. Then you can have rules to document certain issues such as supplier defects or line-down situations.
 
Q

QAMTY

Thanks Dramman

You are right, that´s the idea, minor nc´s, should be fixed on the fly.

The rules for certain issues is what is very important, that is what I´m looking for.
Do you have some rules to share?

Thank you
 

Mark Meer

Trusted Information Resource
We have slightly different systems depending on occurrence rates and activity involvement:
Frequent = Easy, little documentation
Infrequent/Involved = More detailed documentation

For example:
- Scrapped NC components: happens all the time.
-- For items where there is little value for us to track (e.g. simple screws/fasteners), people can just scrap these.
-- For higher-cost items (where we'd like to gather data on yield), there is a simple spreadsheet logging the quantities scrapped. It takes all of a few seconds to make an entry before scrapping the identified NC item.

- Reworked NC components: less frequent.
-- For this, we do want to gather data, the value being that it can be involved process, and data is needed to do cost-benefit.
-- Again, though, we don't want to make documentation burdensome, so a spreadsheet is used, with just a few more columns than the scrapped items.

As DRAMMAN suggests, you can make the rules, and I'd suggest the first step is to identify what data is of value to you.

If people fix things on the fly, and you've got controls to ensure that everything is conforming prior to delivery, AND you don't see yourself needing/wanting to analyze data regarding the occurrences of such events, then why burden yourself unnecessarily?

MM.
 
D

DRAMMAN

I think it is going to vary by company and what you are trying to accomplish. Many companies are going to have multiple systems to track non-conformances. When I worked at a large corporation we had many systems to document and track non-conformances with thousands of NC's being recorded every day. It is really going to be up to each organization to decide which non-conformances are of value to track. Some companies may elect to only track customer complaints. Others may track many types of non-conformances such as scrap, test failures, line defects, supplier defects, etc.

From an auditing perspective it would be up to your auditor to evaluate your NC system. As an example, if you were a 500 employee factory and said you do not need to track non-conformances that would likely be challenged.

Smaller organizations may have a simple spreadsheet or Access database to record and track NC's.
 
R

ReworkIT

The LEAN gods are rolling their collective eyes! Not recording instances of non-conforming product is ignoring a form of waste. Aren't you confusing the cost of the actual component - a fastener - with the (true) cost of getting it into the hands of the operator? Isn't is supposed to work? "Right First Time"? If you don't at least put an "X" on a tally sheet of defects, isn't that wrong? I don't know, but our LEAN champion would be getting excited over this one, even if ISO auditors don't.
 
Q

QAMTY

Thanks to all.
Dramman.

what you or Mark Meer suggest it sound interesting.
If I can catch the concept is like this.

Lets say when we detect a nc, whatever minor or major, first to register it in an excel file but not to fill out an NCR format for every Nc unless its is medium or big the problem, only to fill it out where it is needed to define the disposition is it ok?
The idea it is that at certain intervals, we have to check the excel file trying to determine the total cost of reworks, scrap for improvements purposes.
is it ok the way I perceive it?.
In fact, I think I can include in my Non conformance procedure that at every month I have to check such file in looking for improvements.
This way I dont have to fill out a lot of NCR formats, thus not wasting time and efforts.

Could you share a template for this?

Thanks
 

Pancho

wikineer
Super Moderator
Hi QAMTY,

If you are in Monterrey, we'd be happy to show you our system for handling NCs. PM me if you'd like to do so.
 
Q

QAMTY

Thanks Pancho

Yes I live in mty, I´ll contact you later to see how you manage this stuff.

Thank you very much
 
Thread starter Similar threads Forum Replies Date
C Practical experience validating CNC Mills Medical Device and FDA Regulations and Standards News 11
G What is considered good (and practical) evidence of supervision ISO 17025 related Discussions 4
Sidney Vianna ISO Practical Guide on ISO 31000:2018 - Risk Management Other ISO and International Standards and European Regulations 0
Bev D Essential References for Practical Quality Engineering Misc. Quality Assurance and Business Systems Related Topics 0
S Practical Implementation of ISO 14971 ISO 14971 - Medical Device Risk Management 6
A What are Practical data center best practices IEC 27001 - Information Security Management Systems (ISMS) 1
N Best practices for capturing audit objective evidence in a practical manner? Internal Auditing 3
B Practical ideas for information labelling in healthcare environment IEC 27001 - Information Security Management Systems (ISMS) 2
M Getting into biotech QA from aerospace - Is it practical? Career and Occupation Discussions 2
Q Practical guide to scan for Risks in all QMS systems without missing any ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 16
Sidney Vianna Blockchain Technology - Any examples of practical application? The Reading Room 21
Cats Clause Practical use of Heat Input calculation for Manual MIG Welding Manufacturing and Related Processes 4
M Practical Methods using Sampling by Variables Inspection, Prints (Drawings), Testing, Sampling and Related Topics 2
R Looking for Practical Advice in Managing Measurement Uncertainties Measurement Uncertainty (MU) 3
WEAVER Is GR&R really practical for a Measurescope? Gage R&R (GR&R) and MSA (Measurement Systems Analysis) 12
A 6 Sigma: Could you share some practical examples of 6 Sigma Projects in your company? Six Sigma 3
A Exploding the Myths Surrounding ISO 9000: A Practical Implementation Guide Book, Video, Blog and Web Site Reviews and Recommendations 28
L oPRP or CCP? Practical example Food Safety - ISO 22000, HACCP (21 CFR 120) 2
L Working closer and better with Suppliers - Practical ideas to improve? Supplier Quality Assurance and other Supplier Issues 8
R Suggestions for a practical way to manage Contract Review Contract Review Process 5
O Practical 8-D or similar Problem Solving worksheet or form Excel .xls Spreadsheet Templates and Tools 5
M Need practical guide on TS 16949 Clause 7.6 Requirement IATF 16949 - Automotive Quality Systems Standard 1
M Practical Guidance on TS 16949 Clause 7.5.3 - Product Status Identification IATF 16949 - Automotive Quality Systems Standard 3
paul van oppen Random Sampling at Receiving Inspection: A Practical Implementation needed Inspection, Prints (Drawings), Testing, Sampling and Related Topics 13
C Practical Examples of completed ISO 19011:2011 Audit Reports General Auditing Discussions 5
T Practical Problem Solving - Does anyone have a practical problem solving template? Document Control Systems, Procedures, Forms and Templates 6
S Practical Data Collection Process Recommendations? Design and Development of Products and Processes 6
S OPRP or HACCP Plan - Opinions and Practical Example Wanted Food Safety - ISO 22000, HACCP (21 CFR 120) 17
S Validation of Production Process - Practical Example ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 7
F Toyota A3 Practical Problem Solving (PPS) Document Needed Nonconformance and Corrective Action 1
L Corrective Action Request Assessment and Prioritisation Criteria - Practical Examples Nonconformance and Corrective Action 14
Q Father Of The Practical CMM, James Coggin (RIP) Coffee Break and Water Cooler Discussions 1
I Practical definition of IEC62304 Software Items and Software Units IEC 62304 - Medical Device Software Life Cycle Processes 7
A Definition Modify, Magnify, Minify, and Substitute - Seeking practical ways of differentiation Definitions, Acronyms, Abbreviations and Interpretations Listed Alphabetically 17
L Please share some practical SPC exercises for training purpose Statistical Analysis Tools, Techniques and SPC 4
M Practical Reasons Behind The ISO 13485/QSR Regulations ISO 13485:2016 - Medical Device Quality Management Systems 6
L Employee motivation and empowerment - Please some practical methods IATF 16949 - Automotive Quality Systems Standard 20
G Practical Screw Thread Information & Tolerances General Measurement Device and Calibration Topics 98
R Practical Problem Solving for Management Development Quality Tools, Improvement and Analysis 3
D Internal Auditing ? A Practical Approach General Auditing Discussions 4
Anerol C Definition Rework vs. Repair - What's the practical difference? Definitions, Acronyms, Abbreviations and Interpretations Listed Alphabetically 43
ScottK How far is it practical to take a Process FMEA? FMEA and Control Plans 14
L Practical Ideas for TS 6.2.2.4 - Personel are aware of the relevance and importance.. Training - Internal, External, Online and Distance Learning 5
M Stakeholder Analysis - Practical success stories wanted ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 5
J Q Leading and Lagging Indicators - Difference (practical) ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 8
Z Design and Development Planning - Is It Sufficient and Practical or Not Design and Development of Products and Processes 0
C Interpretation and Practical Application of ISO 17025 - Development of a System ISO 17025 related Discussions 81
G Practical examples of VOC and CTQ flowdown Six Sigma 8
D What practical measures can be taken to improve customer satisfaction? Customer and Company Specific Requirements 21
Govind Here is a Practical Test for QMS Effectiveness ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 5

Similar threads

Top Bottom