SBS - The best value in QMS software

Interesting Discussion How to Deal with Suppliers Who Refuse to Complete our ISO Survey?

dubrizo

Involved In Discussions
#41
@QC Geek,

Most organizations classify suppliers based on commodity, criticality, spend, safety, risk, etc.

The way I look at is is this: how does what you (vendor) supply impact or potentially effect my (customer) end product?

Using your example: a copy machine, most of the time, is not directly impacting product quality. There are always exceptions to this. Whereas a machine tool has the ability to greatly impact your end product, yield, etc.
 
Elsmar Forum Sponsor

optomist1

A Sea of Statistics
Super Moderator
#42
note to self.....remember this when the next source selection committee convenes/asks for input....cooperative nature is of great value when working with suppliers. Most firms maintain a supplier matrix....used to evaluate each, and used to compile future bidders list for source packages
 
Q

QC_geek

#43
There is a difference. The copy machine is not used to produce product.
A copy machine could be used to print manuals. If the manual has an error, for whatever reason; it's the responsibility of the provider to ensure compliance and not the people they buy from.

My point being, the "supplier" of a product needs to ensure compliance of what THEY build or provide in service.
 
Q

QC_geek

#44
@QC Geek,

Most organizations classify suppliers based on commodity, criticality, spend, safety, risk, etc.

The way I look at is is this: how does what you (vendor) supply impact or potentially effect my (customer) end product?

Using your example: a copy machine, most of the time, is not directly impacting product quality. There are always exceptions to this. Whereas a machine tool has the ability to greatly impact your end product, yield, etc.
YES, if the machine is used improperly it can produce a bad output...but just as a car supplier is NOT responsible for how you drive...we are not responsible for how YOU use the equipment.

Once our equipment is installed and signed off...it's theirs to do as they please and completely out of our ability to effect.

Should the equipment fail somehow, it's THEIR responsibility to again verify compliance to their customer.
 

Al Rosen

Staff member
Super Moderator
#45
A copy machine could be used to print manuals. If the manual has an error, for whatever reason; it's the responsibility of the provider to ensure compliance and not the people they buy from.

My point being, the "supplier" of a product needs to ensure compliance of what THEY build or provide in service.
And as part of that process they evaluate the relative risk and plan appropriately.
 

Al Rosen

Staff member
Super Moderator
#46
YES, if the machine is used improperly it can produce a bad output...but just as a car supplier is NOT responsible for how you drive...we are not responsible for how YOU use the equipment.

Once our equipment is installed and signed off...it's theirs to do as they please and completely out of our ability to effect.

Should the equipment fail somehow, it's THEIR responsibility to again verify compliance to their customer.
When you buy an automobile, you consider the manufacturer's reliability history.
 
Q

QC_geek

#47
And as part of that process they evaluate the relative risk and plan appropriately.
OK...so how does that make an equipment supplier part of that equation? They determine whatever RISK via their process...again completely out of our ability to effect change.

BTW...we manage suppliers without the use of a "Survey" and we have thousands.

Product that is used in our equipment is constantly monitored, but we have never (in 16 years doing this) included ANY equipment purchase we've made (and we have hundreds).

The entire point in having an AVL and requesting this information from "Suppliers" is to ensure congruity of product you are typically sampling and you don't need surprises when something shows up and now stops production or worse causes a problem for our customer.

These surveys all focus on ensuring they can rely on that continued congruity...my equipment is singular, not ongoing; subject to improper use...doesn't require a license.

ISO needs a better definition...it's too vague.
 

Al Rosen

Staff member
Super Moderator
#48
OK...so how does that make an equipment supplier part of that equation? They determine whatever RISK via their process...again completely out of our ability to effect change.
For example, the customer may want to know that if they need service you will be there in the future. If you don't like filling out the survey don't.
 
I

Illek

#49
Our office equipment vendor is listed as a service provider for repairs we may need and value for service. We have to evaluate services as well as products now but depending on the risk profile of the service we don't request questionnaires from all service providers. Besides that I know we will not get back questionnaires we send out so if we don't get one it just may increase their risk. It doesn't mean the service provider won't ever be used again.
 

Wes Bucey

Prophet of Profit
#50
There is a difference. The copy machine is not used to produce product.
Actually, engineers and designers use copiers and printers to produce their work product for distribution as well as computers and (in many cases) fax machines. The quibble is not about the supplier's product, but about ANY change in that product which "may" affect the operation or product of the buyer (form, fit, function, price, training to use, etc.) Every product is unique in the effect a change may have on the buyer's product or operation. Once that is made clear to the supplier, he may be more cooperative. It also means each query to the supplier should be unique - no "one size fits all" questionnaires!
 
Thread starter Similar threads Forum Replies Date
N How to deal with catalog parts suppliers who refuse to submit PPAP documents? APQP and PPAP 0
F Circuit board FAI reports- How do you folks deal with these? Inspection, Prints (Drawings), Testing, Sampling and Related Topics 0
L How to deal with an ISO 13485 Supplier Audit nonconformance ISO 13485:2016 - Medical Device Quality Management Systems 17
MDD_QNA How to deal with FDA after not reporting anything for several years Other US Medical Device Regulations 14
M Informational Update from GOV.UK – Regulating medical devices in the event of a no-deal Brexit – UK Responsible Person Medical Device and FDA Regulations and Standards News 0
A How to deal with changed shared components in 510k 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 2
M Informational UK – Contingency legislation covering regulation of medicines and medical devices in a no deal scenario – Human Medicines and Medical Devices (Amendm Medical Device and FDA Regulations and Standards News 3
M Informational EU – Medicinal products and medical devices: Coordinated approach in case of a withdrawal of the United Kingdom from the Union without a deal Medical Device and FDA Regulations and Standards News 0
M Informational UK – Regulating medical devices in the event of a no deal scenario Medical Device and FDA Regulations and Standards News 0
M Informational UK – Businesses supplying medicines and medical devices – what to expect on day one of a ‘no deal’ scenario Medical Device and FDA Regulations and Standards News 1
M Informational Design for new product safety marking for the no-deal Brexit scenario Medical Device and FDA Regulations and Standards News 1
M Informational UK – Contingency legislation covering regulation of medicines and medical devices in a no deal scenario Medical Device and FDA Regulations and Standards News 1
M Medical Device News MHRA releases response to consultation on EU exit no-deal legislative proposals Medical Device and FDA Regulations and Standards News 0
M Pharmaceuticals News UK – Further guidance note on the regulation of medicines, medical devices and clinical trials if there’s no Brexit deal Medical Device and FDA Regulations and Standards News 0
M Medical Device News Letter to the health and care sector: update on preparations for a potential no-deal Brexit Medical Device and FDA Regulations and Standards News 0
supadrai Indemnity Letters - What's the Deal? Other Medical Device and Orthopedic Related Topics 5
M Medical Device News MHRA to consult on EU exit no-deal legislative proposals EU Medical Device Regulations 1
D How to deal with user needs when it is obvious the design meets the user need 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 5
P Quality Assurance and Quality Control - Which clauses of ISO 9001 deal with each? ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 3
O How to deal with Multiple Datums - Position with respect to Multiple Datum Feature Inspection, Prints (Drawings), Testing, Sampling and Related Topics 7
J ISO 9001:2015 Clause10.2 Nonconformity and Corrective Action - Deal with Consequences ISO 9000, ISO 9001, and ISO 9004 Quality Management Systems Standards 2
0 How to deal with resistance to GDP Document Control Discipline Document Control Systems, Procedures, Forms and Templates 7
R How to deal with CONFIDENTIAL documents Document Control Systems, Procedures, Forms and Templates 2
L How to deal with resistance from auditee(s) Internal Auditing 20
P How to deal with a Recruitment Consultant Career and Occupation Discussions 3
AnaMariaVR2 3 Ways To Deal With People Who Play Office Politics Against You Coffee Break and Water Cooler Discussions 7
J How to deal with incomplete forms Nonconformance and Corrective Action 14
R How to deal with the RM requirement of clause 17 Electromagnetic Compatibility? IEC 60601 - Medical Electrical Equipment Safety Standards Series 8
L How to deal with too many CARs (Corrective Action Requests), PARs (Preventive Action) Nonconformance and Corrective Action 25
T How to train employees to deal with external auditors? Internal Auditing 13
S Training on how to deal with Regulations, Rules, Regulations Conflicts, etc. Training - Internal, External, Online and Distance Learning 6
M Mobile Medical Platforms - How to deal with Supplier Hardware/Software Changes? 21 CFR Part 820 - US FDA Quality System Regulations (QSR) 2
S How to deal with non-compliant company after take over of them IEC 27001 - Information Security Management Systems (ISMS) 6
C If my location does not deal with GM - Firewall - CS1 & CS2 Question IATF 16949 - Automotive Quality Systems Standard 3
I How to deal with Behaviour Problem in the work place? Human Factors and Ergonomics in Engineering 20
J How to deal with Mental models IEC 62366 - Medical Device Usability Engineering 1
BradM Deal? Or no Deal? Coffee Break and Water Cooler Discussions 25
Marc Looking for a good deal on a boat? World News 2
S How to deal with telemarketers Funny Stuff - Jokes and Humour 2
ScottK Giving training with a vicious cold - how do you deal? Training - Internal, External, Online and Distance Learning 9
Marc Delphi to close, sell most plants under deal World News 0
J How to deal with an employee who has a bad attitude? - Employee Attitudes Coffee Break and Water Cooler Discussions 15
D X Bar Chart - How can I deal with missing values in subgroups Statistical Analysis Tools, Techniques and SPC 12
E Lets Make a Deal... The TV show - A statistical approach Coffee Break and Water Cooler Discussions 8
M Dock to Stock - How to deal with inspection status requirements Inspection, Prints (Drawings), Testing, Sampling and Related Topics 1
Marc Delphi, GM and UAW reach broad buyout deal World News 1
I How to deal with and track Customer Specific Requirements Customer and Company Specific Requirements 6
J How to deal with operators who fail to follow work instruction? Misc. Quality Assurance and Business Systems Related Topics 52
W Who is my customer? We only deal with the agent who sells our plastic resins IATF 16949 - Automotive Quality Systems Standard 14
P Is TS-16949 a 2 for 1 Deal? QS-9000 - American Automotive Manufacturers Standard 6

Similar threads

Top Bottom