S
Hi everyone,
I work in a subcontractor which is not design responsible. We have the following partnership with our client:
We use its equipment, materials, work instructions, most of its procedures are mandatory to us and so on
We are not design responsible - we only assemble,test,inspect,pack and deliver the finished goods.
We are now going to work on implementing QS according ISO 16949.
But our main problem is to define exactly what can we use from our client as documents(like said they are mandatory to us):
for example they have distributed a copy of their Control Plan and we work according to it - do we need to develop our own as one of the mandatory documents needed?
And one more is it necessry for our client to put signatures to our additional procedures if such are needed for us - for example there are unapplicable points in some of their procedures for us as our production is smaller in processes and quantity.
Have anyone been in such situation and can share experience?
I work in a subcontractor which is not design responsible. We have the following partnership with our client:
We use its equipment, materials, work instructions, most of its procedures are mandatory to us and so on
We are not design responsible - we only assemble,test,inspect,pack and deliver the finished goods.
We are now going to work on implementing QS according ISO 16949.
But our main problem is to define exactly what can we use from our client as documents(like said they are mandatory to us):
for example they have distributed a copy of their Control Plan and we work according to it - do we need to develop our own as one of the mandatory documents needed?
And one more is it necessry for our client to put signatures to our additional procedures if such are needed for us - for example there are unapplicable points in some of their procedures for us as our production is smaller in processes and quantity.
Have anyone been in such situation and can share experience?