D
dobs
Hello,
I am relativly new in that topic so these questions might sounds stupid to you.
Several month ago our Department was sold to an other company. But the manufacturer of our development product is still our former company and they neither make PPAP nor controlplans what our new company wants us to do according to QS9000. So we are in a conflict.
PPAP documents have to be archived by the manufacturer so we do have to give them our PPAP relevant documents. Am I right here or do we have to archive all PPAP documents becausewe sell the product?
Now our auditor wants us to create a PPAP-reference-list for our manufacturer who doesn´t need it. Even if we do this list who takes care of it´s updates?
As a developer of electronic control units we have to create some documentes for our manufacturer. Is it possible to refern on quality instructrions of our manufacturer within our quality documents? For instance: Our manufacturer wants us to tell them whether our product is okay or not, so we´vge got to do some so called "qualiy evaluations" (reviews) during our development phase and one within the factory befor serial introduction. That is completely different from instructions of our new company.
It´s all a bit confusing, hopefully I could make it clear enough to you.
Please give me a note if you know some hints to untangle all these stuff.
Unfortunately there is an certifcation audit in about 3 weeks. In my opinion too early for a company which has to change all its process but I can´t do anything about it.
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dobs
I am relativly new in that topic so these questions might sounds stupid to you.
Several month ago our Department was sold to an other company. But the manufacturer of our development product is still our former company and they neither make PPAP nor controlplans what our new company wants us to do according to QS9000. So we are in a conflict.
PPAP documents have to be archived by the manufacturer so we do have to give them our PPAP relevant documents. Am I right here or do we have to archive all PPAP documents becausewe sell the product?
Now our auditor wants us to create a PPAP-reference-list for our manufacturer who doesn´t need it. Even if we do this list who takes care of it´s updates?
As a developer of electronic control units we have to create some documentes for our manufacturer. Is it possible to refern on quality instructrions of our manufacturer within our quality documents? For instance: Our manufacturer wants us to tell them whether our product is okay or not, so we´vge got to do some so called "qualiy evaluations" (reviews) during our development phase and one within the factory befor serial introduction. That is completely different from instructions of our new company.
It´s all a bit confusing, hopefully I could make it clear enough to you.
Please give me a note if you know some hints to untangle all these stuff.
Unfortunately there is an certifcation audit in about 3 weeks. In my opinion too early for a company which has to change all its process but I can´t do anything about it.
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dobs