SBS - The best value in QMS software

Who has TS 16949?

C

Carlos

#1
#1
I'm from Chihuahua, Mexico. Our company is trying to implement the new spec TS 16949, but we don't know how to make the transition from QS-9000 to TS16949.

Some one know how to make it?
 
Elsmar Forum Sponsor
A

Al Dyer

#2
#2
Please don't think me impertinent, but since you are already QS-9000, what does your auditor/registrar say about the process?

Just looking for knowledge!
 
S

Sporty

#3
#3
I would start with a gap analysis of QS9000 to TS16949. There is not that big a difference. (just my opinion)
Once you see the gaps, you can start making the changes necessary to be compliant to TS16949.
You have a choice of rewriting your procedures into the new "process oriented" format, or just keep them with the old 20 sections, and create a matrix showing where the applicable "shalls" are covered.
We have TS16949:99 here, and I'm just in the middle of creating that matrix to TS16949:2002.....
Some of the areas I noticed needed "beefing up" were Internal Auditing, In house Laboratory (for QS to TS), Customer Focus, Management Review and Internal/Customer Communication.

Good Luck....:D
 
R

Roger Eastin

#4
#4
Sporty is right on. There is not that much of a difference. If you have had any exposure to VDA6, you'll notice its influence. Create your matrix(QS vs TS-2002 comparison) and do a gap analysis. I thought we had something like that here in the cove already. Do a search and also look in the pdf library.
 
C

Carlos

#5
#5
There is a procedure to make the transition from QS9000 to TS16949?. We are certified since 1999, and we took some courses for TS, but it was very clear, is the reason that we are need help about it.

I was wondering if some one can help us.
 
K

keyplas - 2006

#6
#6
Yet another unknown.....

Ok here is my wonderful "Confused by the ISO MAFIA" question...the Big 5 and several Tier One's have made the statements about upgrading to TS soon (I've seen Dec 2002-2003-2006 all from GM) But irregardless Visteon for exapmle has said yes be transitioned third party by the middle of next year, If the version 2 of TS was just released 5/28, and not many Auditors are trained on it yet...can I roll up the cost of the transition to an already obsolete specification into my part cost because thy are being pig headed about all of this? If in the case of visteon, I only transition to the 1st version of TS will I still be losing the 5 points on my quality rating anyway? Shoot me now or give me your feelings on what this situationis all about...By the way , anyone know of a registrar that wants a nice sized account that won't rob me on "Incidental" costs?
 
M

Manoj Mathur

Quite Involved in Discussions
#7
#7
There is a beutiful Gap Analysis with ref to TS-16949. You can use and see for the diffefence between two. I got more stuff on this difference between two Automotive standards, ISO/TS 16949:2002 vs. QS 9000. But at this time see attach file for Gap Analysis.
eye I want to attach the file; How do i do??????
 
M

Marjie James

#8
#8
I also have a gap analysis available to anyone who is transitioning from QS-9000 to TS 16949:2002. If I don't figure out how to post it, you may contact me for a copy of my analysis.
Regards
Marjie :D
 
Last edited by a moderator:
M

Marjie James

#9
#9
How to add an attachment - Gap Analysis

From the FAQ page:

To attach a file to a new post, simply click the [Browse] button at the bottom of the post composition page, and locate the file that you want to attach from your local hard drive.

This is available when posting a reply but not when you edit.

I am attaching my gap analysis of TS v/s QS. The last column will show an asterick if there were any changes from the draft version, even if it was a wording change.

Regards
Marjie
 

Attachments

You must log in or register to reply here.
Thread starter Similar threads Forum Replies Date
Sidney Vianna Informational UTC ASQR Rev.11 has a mistake; certification of distributors to IATF 16949 AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 0
S Has anyone completed IATF 16949 Certification - Share your Audit Experience? IATF 16949 - Automotive Quality Systems Standard 2
M Who has had a Transition Audit from TS 16949 to IATF 16949 IATF 16949 - Automotive Quality Systems Standard 120
Q TS 16949 Clause 7.3.2.3 when the Customer has no Special Characteristics IATF 16949 - Automotive Quality Systems Standard 25
Howard Atkins Ford India has ISO/TS 16949 IATF 16949 - Automotive Quality Systems Standard 4
T Has anyone found the "TS 16949 Rule Book" helpful? IATF 16949 - Automotive Quality Systems Standard 3
C Supplier has different ISO 9001 certification scope and TS 16949 certification scope Supplier Quality Assurance and other Supplier Issues 15
A ISO TS 16949 Certification Rules - Ensuring that all ISO/TS aspects has been audited IATF 16949 - Automotive Quality Systems Standard 1
I TS 16949 - What nonconformances has everyone seen from your audits? IATF 16949 - Automotive Quality Systems Standard 2
T TS 16949 vs. Dock to Stock - Seeking comments from anyone who has implemented DtS IATF 16949 - Automotive Quality Systems Standard 4
A What exactly has to be included in a TS 16949 records matrix IATF 16949 - Automotive Quality Systems Standard 4
J TS 16949 - Has anyone used this form for your COPS, MOPS & SOPS? Document Control Systems, Procedures, Forms and Templates 4
T Has ISO/TS 16949 Been Revised? IATF 16949 - Automotive Quality Systems Standard 14
C TS 16949 vs. ISO 9001 - Differences - TS 16949 has more requirements ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 4
T The IAOB's TS 16949:2000 FAQ has been Updated IATF 16949 - Automotive Quality Systems Standard 1
A Has Toyota Approved ISO / TS 16949? IATF 16949 - Automotive Quality Systems Standard 2
J How to keep MDD certificate valid when legal manufacturer has liquidity problem EU Medical Device Regulations 0
K Should APQP/PPAP has its own section in a QM? Quality Management System (QMS) Manuals 1
G Special 510K possible? Only the packaging has changed Other US Medical Device Regulations 0
Louddogsbark When your 13485:2016 certificate has been pulled ISO 13485:2016 - Medical Device Quality Management Systems 2
lanley liao What shoud i do if our company top management has been changed. Oil and Gas Industry Standards and Regulations 8
S PSW - Requirements for "off-the shelf" component that has multiply manufacturing locations Off the Shelf Item Manufacturing and Related Processes 1
L GRR for a tolerance that has changed Gage R&R (GR&R) and MSA (Measurement Systems Analysis) 6
D Partial FAI - AS9102 - One single drawing has 10 part numbers AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 5
BeaBea ISO 9001 Customer Feedback Methods - What has worked for your company? Service Industry Specific Topics 17
S Has anybody done IMS - Management Review Meeting ISO 14001:2015 Specific Discussions 8
M Has anyone has been through an MDR audit? (3/2020) EU Medical Device Regulations 1
M Has anyone heard of Run at Risk? Manufacturing and Related Processes 15
B ASA Aviation Supply Association - Has anyone heard of ASA? AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 1
B Has anyone done an IEC 60601-1 gap analysis to IEC 60335? Medical Device and FDA Regulations and Standards News 4
Z 510(k) usage - Company has 2 physically similar products Medical Device and FDA Regulations and Standards News 2
D Has anyone had sudden challenges from Korea-MFDS? Other Medical Device Regulations World-Wide 1
Sidney Vianna IAQG News IAQG has a new website - December 2019 AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 0
Richard Regalado ISO 22301:2019 has been published - Nov 2019 Business Continuity & Resiliency Planning (BCRP) 0
S FAIR - If we have not produced a part in over 2 years, but nothing has changed AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 5
Nicole Desouza Who has to be compliant with REACH Declarations? REACH and RoHS Conversations 11
CycleMike GD&T - Hole pattern - Print (attached) has a single Datum Reference Frame Inspection, Prints (Drawings), Testing, Sampling and Related Topics 2
A Would an MRP system that has been in use for over 10 years require validation? ISO 13485:2016 - Medical Device Quality Management Systems 6
W Informational VDI 2017 - Medical Grade Plastics - German VDI has published a "Richtlinie" Other Medical Device Related Standards 1
D FDA Biomarker Qualification Program - Has anyone prepared an application? Medical Device and FDA Regulations and Standards News 0
U Hand-Held dosing device has no PATIENT - Interpretation of the PATIENT definition IEC 60601 - Medical Electrical Equipment Safety Standards Series 6
L Has anyone heard of the 2 pan system? Manufacturing and Related Processes 6
N Technical File Reviewer has requested more testing to ISO 10993 Other Medical Device Related Standards 10
I Who has had to move from ISO 9001:2015 to ISO 13485 and what were the challenges? ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 7
M Informational Health Canada has launched an e-Learning tool to aid in understanding the premarket regulatory requirements for medical devices in Canada Medical Device and FDA Regulations and Standards News 0
M Has anyone here assessed the latest Abbreviated 510(K) guidance document? 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 1
M Does anyone has a good verification and validation plan template? ISO 13485:2016 - Medical Device Quality Management Systems 3
lilybef FDA and Biocompatability Testing - Reviewer has requested implantation testing Other Medical Device Related Standards 11
D Has anyone undergone a BARDA (HHS) audit as part of their grant process? Other Medical Device Regulations World-Wide 0
Sidney Vianna LinkedIn bug - Anyone has any idea of how to fix this? Posts not showing for me in a Group feed. Coffee Break and Water Cooler Discussions 2

Similar threads

Top Bottom