SBS - The best value in QMS software

Extra registrar audit days due to Nonconformances?

Stijloor

Staff member
Super Moderator
#11
Thanks to tyker for correcting me! I forgot this thread was in the TS area. He is right the automotive industry writes its own rules!

I still think it is garbage though!:lol:
Paul,

With all due respect:

The IATF has worked hard to create a "world-wide" constant approach in ISO/TS 16949:2002 certification audits and auditor training. They have the whole certification process documented in what we know as "The Rules." Something that was greatly missing during the QS-9000 era where gross inconsistencies were rampant. As a result, the automotive customers did not get what they were looking for. The IATF decided to take the certification process into their own hands.

Yes, it may be tough..but so far it has worked.

Stijloor.
 
Elsmar Forum Sponsor

Paul Simpson

Trusted Information Resource
#12
With all due respect:
Whenever I hear / read that at the start I know the boot is coming. :lmao:

The IATF has worked hard to create a "world-wide" constant approach in ISO/TS 16949:2002 certification audits and auditor training. They have the whole certification process documented in what we know as "The Rules."
We agree so far - there are a lot of rules. :)
Something that was greatly missing during the QS-9000 era where gross inconsistencies were rampant.
Again, with respect, :D there were a lot of rules in the "bad old" days of QS. I used to quote / audit / train auditors in accordance with the rules. Like all things there are people who work to the rules and people who do not. As an individual (and the CB I worked for at the time) I / we believed in working to the rules - even the stupid ones. :tg:
As a result, the automotive customers did not get what they were looking for. The IATF decided to take the certification process into their own hands.

Yes, it may be tough..but so far it has worked.

Stijloor.
In this letter to Quality World magazine I question whether it has worked (to read the article you have to register but some points are reproduced below).

The automotive industry is not practising what it preaches to its supply base of establishing and eliminating root cause. I believe that third party certification is used to paper over cracks where original equipment manufacturers (OEMs) are not communicating effectively with suppliers on product requirements and production control systems.
The move to TS 16949 represents an opportunity lost for the automotive industry. Unless it understands what it expects from the certification process and what it needs to do (jointly with industry, accreditation, certification bodies and suppliers) then TS 16949 certification will continue to underperform in its eyes.
I have plenty of examples of where CBs are seen to obey the letter of the rules without meeting the spirit of requirements and the oversight by the "industry body" would never know because the nice neat reports showed it is OK.

I'll just leave you with one little teaser. One largish organization passed their TS surveillance audit in the time it took a friend of mine to get a coffee from the machine! :mg:
 
T

tyker

#13
I'll just leave you with one little teaser. One largish organization passed their TS surveillance audit in the time it took a friend of mine to get a coffee from the machine! :mg:
At the risk of straying widely :topic: this is clearly unbelievable news.
You have a friend? :notme:


Back, however, to Domoreto's concern.
Everybody should remember that CBs, despite their protestations to the contrary, have no divine right to bully their customers. Any organization which believes it is being treated unfairly by a CB should challenge, protest, scream and do whatever it takes to bring them to their senses.

A 40% increase in surveillance time to clear 4 minors is outrageous and, if Domoreto succeeds in getting this overturned, and the CB applies proper corrective action to the root cause of their failing, other organizations may be spared this iniquity.
 
Last edited by a moderator:

Stijloor

Staff member
Super Moderator
#14
Whenever I hear / read that at the start I know the boot is coming. :lmao:

We agree so far - there are a lot of rules. :)
Again, with respect, :D there were a lot of rules in the "bad old" days of QS. I used to quote / audit / train auditors in accordance with the rules. Like all things there are people who work to the rules and people who do not. As an individual (and the CB I worked for at the time) I / we believed in working to the rules - even the stupid ones. :tg:
In this letter to Quality World magazine I question whether it has worked (to read the article you have to register but some points are reproduced below).

I have plenty of examples of where CBs are seen to obey the letter of the rules without meeting the spirit of requirements and the oversight by the "industry body" would never know because the nice neat reports showed it is OK.

I'll just leave you with one little teaser. One largish organization passed their TS surveillance audit in the time it took a friend of mine to get a coffee from the machine! :mg:
Paul,

Thank you for your response and excellent points.:yes:

You and I have different ISO/TS experiences and viewpoints. That's great.

I admit that ISO/TS (its requirements, implementation and audits) is not perfect. No QMS standard is. Each of us can come up with examples why it works and why it does not work. I can only go by what I have personally experienced.

Compared to QS-9000, I believe strongly that ISO/TS and "The Rules" have created a (greatly improved) level playing field.

I work hard with my Clients to make it work for them. That's all I can do, and will continue to do so.

Stijloor.
 

howste

Thaumaturge
Super Moderator
#15
I have never added more than an hour to a TS audit to close prior (minor) nonconformities. Adding a half day or more would be excessive in my opinion.
 
T

tyker

#16
Talk about coincidences!

At the end of last week, the external auditor for one of our associate plants overseas gave us the audit plan which included an arbitrary increase in the surveillance visit duration of 50% (2 days to 3 days) to review corrective action from the previous visit. The plan arrived only 2 working days before the planned start of the audit and he expected our management to change their schedules to accommodate it.

In my opinion, none of the nonconformities raised previously require any special action on the part of the auditor. Everything can be covered as part of his normal audit activity.

So, a quick telephone call to the guy who heads up TS operations at the CB and, suddenly, we're back to 2 days.
 

Domoreto

Registered Visitor
#17
Hi again.
It seems interesting discussion took place here....
Thanks for all the advise and support . I'm on the phone with the registrar and despite them being surprised from my disobedience, I think we are talking...
Concerning " The Rules" of TS16949 - yes, they did bring some structure but at the same time if you supply more than one OEM - you still need to obey and follow all the "specific customer requirements" ...which is ..... a back to the chaos move anyway ...
Personal opinion. :cool:
 

try2makeit

Quite Involved in Discussions
#18
Hi again.
It seems interesting discussion took place here....
Thanks for all the advise and support . I'm on the phone with the registrar and despite them being surprised from my disobedience, I think we are talking...
Concerning " The Rules" of TS16949 - yes, they did bring some structure but at the same time if you supply more than one OEM - you still need to obey and follow all the "specific customer requirements" ...which is ..... a back to the chaos move anyway ...
Personal opinion. :cool:
My last auditor did both, Customer specific and TS16949. And most of our NC's are Customer specific driven.
 
T

tlonkey

#19
I have been audited to ISO - QS - TS - AS at various times and the only instance where our CB had to add additional time to our audit schedule was because of a major non-conformance finding. The CB auditor came back to our facility to do an on-site audit to verify the corrective actions taken to resolve the major nc. Not knowing your situation I can't say for certain but if there were no major issues involved it would be hard to believe that another day would be required to review any non-conformance from your last audit schedule.

tlonkey
 
Thread starter Similar threads Forum Replies Date
D Adding an extra Label on an Ethylene Oxide Sterilized Box ISO 13485:2016 - Medical Device Quality Management Systems 3
M Risk Management File for Extra Oral RX Equipment ISO 14971 - Medical Device Risk Management 11
H Extra checks to do when reviewing the batch records for release of products Records and Data - Quality, Legal and Other Evidence 2
R Going to the bank-How much extra have I paid Funny Stuff - Jokes and Humour 2
G 12 or 13 Men - Where does the extra man come from? Brain Teasers and Puzzles 5
bobdoering "It's just extra paperwork" Imported Legacy Blogs 1
eternal_atlas Are implementation of Quality and Safety Standards Extra Business Costs? ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 16
F Extra Cost for ISO/TS 16949 in Tooling Cost Break Down IATF 16949 - Automotive Quality Systems Standard 11
J What Hardness for .090 Thick Silicone Bronze, Extra Hard Temper (cda 65500-h06) Manufacturing and Related Processes 5
C Extra year of Experience Landed me a Phone Interview Career and Occupation Discussions 12
V Can anyone explain the extra requirements of AS9120 vs. AS9100? AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 10
R Looking for an AS9100 Rev B book - Something that explains all the extra requirements Book, Video, Blog and Web Site Reviews and Recommendations 5
S Extra Time Needed for Audits? ISO 14001:2004 General Auditing Discussions 9
Marc Rational calendar with 364 days - Extra week celebrating Isaac Newton Coffee Break and Water Cooler Discussions 0
M AS9100D Registrar pre-audit requirements AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 15
G 0 non conformities in registrar audits over 4 years Management Review Meetings and related Processes 12
M Do AS9100 Registrar Auditors have nonconformity quotas? General Auditing Discussions 18
J Conflict of Interest Registrar/Notified Body/Testing House Quality Manager and Management Related Issues 4
R Change Notification - Registrar vs Notified body ISO 13485:2016 - Medical Device Quality Management Systems 1
Robert Stanley Which Registrar Should I Choose for ISO 9001:2015 registration? Registrars and Notified Bodies 10
E Choosing an ISO 9001 registrar with auditors familiar with our industry Registrars and Notified Bodies 10
L Audit boundaries - Is a Registrar permitted to audit a company's QMS by visiting their suppliers? AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 26
Jen Kirley Is your registrar (CB) accredited? ASQ, ANAB, UKAS, IAF, IRCA, Exemplar Global and Related Organizations 9
K Seeking ISO 13485 Registrar Recommendations Registrars and Notified Bodies 15
P Notify Registrar of Escalation letter IATF 16949 - Automotive Quality Systems Standard 1
M New AS9100 Registrar - Recommendations for Transfer Registrars and Notified Bodies 3
M Notifying Registrar of Significant QMS changes ISO 13485:2016 - Medical Device Quality Management Systems 2
A ISO 9001:2015 registrar Auditor requesting copies of procedure prior to audit ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 24
N Does anyone know a registrar that offers both ISO 9001 and ISO 17020? Registrars and Notified Bodies 6
S Certification Body, Registrar, Notified Body - What is the difference? Registrars and Notified Bodies 3
1 ISO Registrar with waste water treatment experience Registrars and Notified Bodies 1
D How can a company transfer their AS certificate from a suspended AS91XX registrar? AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 4
P Delay in IATF 16949 Certification from Registrar Registrars and Notified Bodies 10
M Should Potential Customer Complaint Outcome Define Registrar NC Rating? ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 8
Q Is a Domain Registrar a Critical Supplier? ISO 13485:2016 - Medical Device Quality Management Systems 11
F Which Medical Device Standard Registrar would you recommend? CE Marking (Conformité Européene) / CB Scheme 5
WCHorn Transfering certificate from Registrar "A" to Registrar "B" ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 8
W Registrar Practices - Audit Plan with Scope, Dates/Times, etc. ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 5
D Breach of Contract from Registrar (Auditor Payment Issue) Registrars and Notified Bodies 18
V Under what circumstances will a Registrar Audit a Company? (ISO 13485 - Canada) Canada Medical Device Regulations 5
M Contacting a "Must Use" (aka Sole Source) Supplier's Registrar Supplier Quality Assurance and other Supplier Issues 6
C Registrar Charges Per CAR Written Registrars and Notified Bodies 18
Q Supplier evaluation for registrar? Registrars and Notified Bodies 2
A AS9100 Registrar Expense Report Practices Registrars and Notified Bodies 3
M Answered; Registrar Dropped ISO 14971 Certification Program; What Now? ISO 14971 - Medical Device Risk Management 4
R Registrar Annual Management Fee Registrars and Notified Bodies 4
L Registrar Audit Report Length General Auditing Discussions 6
A AATT Aerospace Auditor Requirements for an AS9100 Registrar AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 10
E Consultant Person who implemented ALSO the Registrar Auditor? Consultants and Consulting 17
L Registrar Audit Scope and Limits ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 9

Similar threads

Top Bottom