Posted by mibusha at the APQP and PPAP Forum .
Can any one help?
We design and build welding assemblies, hemmer assemblies and fastening
systems. As a TE supplier we are registering to ISO 9001 TE with a
pre-assessment in January,99.
We have been doing Control Plans and FMEAs (actually catching up on them with
a combination of workshops and classes).
I know we have to have a quality plan and we have to design in R&M. Basically I
am using pages 2-2 through 2-5 in the R&M Guidelines (SAE).
My question is: What form or format does the quality plan and/or R&M take? Do
all five stages appear on a Gantt chart? Must I document, for example, LCC
calculations? Or should I write the procedure (our quality plan and/or R&M)in text
form and note each document as it is mentioned in the text? We do most of the
TE requirements but have not done a good job of documenting them.
As you can see I could use some advice on this. Any help would be appreciated.
Thanks,
Michael
Can any one help?
We design and build welding assemblies, hemmer assemblies and fastening
systems. As a TE supplier we are registering to ISO 9001 TE with a
pre-assessment in January,99.
We have been doing Control Plans and FMEAs (actually catching up on them with
a combination of workshops and classes).
I know we have to have a quality plan and we have to design in R&M. Basically I
am using pages 2-2 through 2-5 in the R&M Guidelines (SAE).
My question is: What form or format does the quality plan and/or R&M take? Do
all five stages appear on a Gantt chart? Must I document, for example, LCC
calculations? Or should I write the procedure (our quality plan and/or R&M)in text
form and note each document as it is mentioned in the text? We do most of the
TE requirements but have not done a good job of documenting them.
As you can see I could use some advice on this. Any help would be appreciated.
Thanks,
Michael