B
BishDamo
I'm new to supplier quality and am confused by the practice of using Approved Vendor Lists. I'm wondering why is it industry practice for some companies to have a list of "approved vendors", if being "approved" says nothing about the ability of that supplier to provide a specific component?
I'm sure it's not uncommon to have an "approved" supplier that has been supplying injection moulded part X for years, but is incapable of consistently supplying injection moulded part Y? In this case, surely the supplier should be on a list of "vendors approved for supply of component X", rather than a list of "approved vendors"? What is the benefit of having a list of "approved vendors" unless it's specific to supply of a particular part? Or another way of looking at it is why can't I just buy from any vendor I like, without any form of AVL, as every time I inspect the component at incoming, am I not "re-evaluating" that suppliers ability to provide the product as required by ISO 9001/13485 (e.g. via Supplier Corrective Action process)?
I do appreciate that there'll obviously be a relationship between a supplier's general systems and their ability to consistently supply quality product, but at the end of the day, isn't it your incoming inspection system that verifies the quality of the components provided? Why waste valuable resources on supplier evaluations and periodic customer audits?
Any info would be much appreciated.
Rgds,
D
I'm sure it's not uncommon to have an "approved" supplier that has been supplying injection moulded part X for years, but is incapable of consistently supplying injection moulded part Y? In this case, surely the supplier should be on a list of "vendors approved for supply of component X", rather than a list of "approved vendors"? What is the benefit of having a list of "approved vendors" unless it's specific to supply of a particular part? Or another way of looking at it is why can't I just buy from any vendor I like, without any form of AVL, as every time I inspect the component at incoming, am I not "re-evaluating" that suppliers ability to provide the product as required by ISO 9001/13485 (e.g. via Supplier Corrective Action process)?
I do appreciate that there'll obviously be a relationship between a supplier's general systems and their ability to consistently supply quality product, but at the end of the day, isn't it your incoming inspection system that verifies the quality of the components provided? Why waste valuable resources on supplier evaluations and periodic customer audits?
Any info would be much appreciated.
Rgds,
D