SBS - The best value in QMS software

How do you justify that not all Suppliers need to be Audited?

M

Murphys Law

#11
Yes, look at which suppliers are critical to your business : In my industry, they are ones that supply raw materials.

We have two levels - Level 1 are ones we regard as strategic or partner suppliers. These are ones that we regard as inovators and bring something to the table.

Level II are ones that could be second sources or ones that we regard as tactical suppliers. They may be tactical in that we don't actively source them due to quality, pricing or technology issues.

It is perfectly acceptable to have regular reviews with a supplier but not necessarily audit them. They key is to give them feedback with an objective scorecard. Strategic suppliers, you may want to have face2face meetings.
 
Elsmar Forum Sponsor
M

munagada

#12
After reading all these replies, i like to add --
ISO-9001 does not tell anything about supplier development, but TS-16949 clearly specifies the supplier development, also gives the CRITERIA -
"the prioritization of suppliers for development depends upon, for example, the supplier's quality performance and the importance of the product supplied"

Your categorization of suppliers (A,B,C,D) may not meeting the TS requirements. For example, your categorization of A,B,C,D may be on the basis of cost, bulk etc. And you start with A-suppliers, but a few D-suppliers whose supplies quality is very important for your product quality, but you ignore them in your supplier development process, you know what the consequence..

Thanks
 
#14
How about "they also have a 3rd party certification to TS16949/ISO9001?"
Since this thread is in the TS forum, Randy's comments need to be considered. TS has some pretty specific requirements. Although, based on the old FAQ, the term "Supplier" was also defined. Look at the requirements for TS on supplier development.
 
R

ralphsulser

#16
Welcome Dear07,

Like Jennifer, I am not sure if you are right to assert that tooling equipment and coolants do not have any effect on the product quality or finished part. Without knowing what you do, I guess it does as in most machining cases.
What we found was that it was more important to control the coolant concentration which contributed more to quality and tool wear. We assigned a full time person to daily monitor and document the concentration levels of each CNC lathing operation. It not only made more consistent cuts, but also improved insert cutting tool life. Lack of this control caused some issues such as chips fused to the part.
 
T

Taliesyn

#17
I've just had exactly this conversation with our External Auditor. We use something like 400 suppliers but three of them account for nearly 92% of all our purchases (for raw materials). I wanted to reduce the amount of work we were doing with a stupidly complex monitoring system that I inherited when I took the job. He had no problem with my proposal and quoted exactly the same sections of the standard quoted above.
 
J

jhoniegudel

#18
In my company supplier monitoring apply for all supplier, but for auditing we done for supplier for direct material which is in bad performance.


jhonie
 
Thread starter Similar threads Forum Replies Date
T How to justify this High %Tolerance Gage R&R (GR&R) and MSA (Measurement Systems Analysis) 3
O How can I justify excluding the R&D group and the design and development clause? ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 4
R PMCF plan to justify that our product not require PMCF study EU Medical Device Regulations 9
Q How can you justify using a more accurate Pin Gage class? General Measurement Device and Calibration Topics 16
D Using R-Chart to justify removal of part from the study Gage R&R (GR&R) and MSA (Measurement Systems Analysis) 8
K CMM Productivity and Internal Rate of Return (IRR) to justify a new Acquisition Inspection, Prints (Drawings), Testing, Sampling and Related Topics 5
S How can I justify adequacy of USB connector soldered on the product Reliability Analysis - Predictions, Testing and Standards 4
K How can I justify adequacy of Frequency of Testing in my Testing Plan Reliability Analysis - Predictions, Testing and Standards 8
C How do I justify outsourced processors - ISO 9001 Clause 4.1 - General Requirements ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 2
R Medical Devices - How to justify the Sampling Plan used? Inspection, Prints (Drawings), Testing, Sampling and Related Topics 3
C How do you justify for that short time of experience? Career and Occupation Discussions 11
W How to justify Widened Control Limits - No Assignable Cause scenario Statistical Analysis Tools, Techniques and SPC 26
G Sample Report to justify additional Document Control workforce Document Control Systems, Procedures, Forms and Templates 3
I Temporary Bandit, Ad Hoc or Rogue Records, Forms, Data, Documents - How to Justify Records and Data - Quality, Legal and Other Evidence 30
C Calibrating Welding Machines - Any way to justify not calibrating the meters? General Measurement Device and Calibration Topics 15
lanley liao Does all of the suppliers need to integrated into the supplier list qualified of the company? Oil and Gas Industry Standards and Regulations 2
M PSA Suppliers - CSR matrix and need the quality manual of PSA APQP and PPAP 3
O How to give a score/yield more correctly to my suppliers Supplier Quality Assurance and other Supplier Issues 12
P Managing How PPAP Requirements are Communicated in the Manufacturing Process and to Suppliers APQP and PPAP 5
B General Motors and Honda Alliance - What does this mean to suppliers? IATF 16949 - Automotive Quality Systems Standard 3
S Conflict Minerals - Tin Suppliers CMRT Miscellaneous Environmental Standards and EMS Related Discussions 4
T ISO 13485 - Process validation at critical suppliers ISO 13485:2016 - Medical Device Quality Management Systems 7
P Mylar plot suppliers in accordance with D6-51991 document AS9100, IAQG, NADCAP and Aerospace related Standards and Requirements 4
T Reaction Plan To Drive suppliers to IATF 16949 registration IATF 16949 - Automotive Quality Systems Standard 6
I Approved Suppliers ISO/IEC 17025:2017 and used test equipment ISO 17025 related Discussions 6
C Critical Suppliers for EU medical device approvals May 2020 EU Medical Device Regulations 1
M Who should receive the bills from suppliers and vendors, account payable or procurement? Consultants and Consulting 4
P Qualifying commercial off the shelf (COTS) external suppliers ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 10
Nicole Desouza Are Shipping Companies Suppliers? Manufacturing and Related Processes 4
J Painted cut threads - ASME Pipe Suppliers Manufacturing and Related Processes 6
G ISO 9001 8.4 applied to 7.1.3 - Suppliers of infrastructure requirements - IT and Print solutions ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 4
P IATF 16949 Clause 8.4.2.3 - Justification for non-certified suppliers IATF 16949 - Automotive Quality Systems Standard 14
J Requirements for customer directed suppliers Customer and Company Specific Requirements 5
R Supplier Controls we can place on Single-Source Suppliers ISO 13485:2016 - Medical Device Quality Management Systems 2
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
R ISO 9001 versus ISO 13485 for Suppliers to Medical Device Companies ISO 13485:2016 - Medical Device Quality Management Systems 2
R Critical suppliers (Definition of) and MDSAP (Medical Device Single Audit Program) ISO 13485:2016 - Medical Device Quality Management Systems 15
P IATF 16949 - Monitoring Suppliers for Premium Freight IATF 16949 - Automotive Quality Systems Standard 12
DuncanGibbons Documentation aerospace OEMs require with purchase of parts from manufacturers/suppliers Manufacturing and Related Processes 0
K Supplier Controls for Animal Tissue Suppliers for Medical Devices Other Medical Device Regulations World-Wide 0
optomist1 Survey of Tier 1 & Tier 2 suppliers APQP and PPAP 6
P Non-Active Suppliers on CE Certificate EU Medical Device Regulations 2
C Suppliers re-classification from Critical to Significant or from Significant to Non-critical Supply Chain Security Management Systems 0
D Training for AS13000 - Problem Solving Requirements for Suppliers Training - Internal, External, Online and Distance Learning 14
eule del ayre List of Level 3 PPAP requirements for automotive suppliers APQP and PPAP 20
Q Does our material suppliers’ supplier have to be at least ISO 9001 certified? IATF 16949 - Automotive Quality Systems Standard 3
N How to deal with catalog parts suppliers who refuse to submit PPAP documents? APQP and PPAP 0
S Outsourcing manufacturing - Who controls the suppliers of parts to the CMO? ISO 13485:2016 - Medical Device Quality Management Systems 2
Ed Panek Supplier Auditing - No purchases from our key suppliers in the last 24 months ISO 13485:2016 - Medical Device Quality Management Systems 5
I IATF 16949 - 8.4.2.3 - Applicability to Shipping Suppliers IATF 16949 - Automotive Quality Systems Standard 11

Similar threads

Top Bottom