Steve.Davidson
Registered
I am in the process of creating a global error proofing process for our 5 semiconductor manufacturing sites, which as you can imagine is not easy, as they all have differing opinions on what constitutes an EP device etc.
Quality Managers for the sites are trying to convince me that IATF requirements for EP does not apply to our industry, as we make billions of products annually, which in my opinion is ridiculous and completely wrong because you cannot just decide to ignore an IATF clause for your own convenience !!.
The processes are many and extremely complex, so my main motivation is to create an EP methodology that works for us and keeps the control plans to a sensible and manageable level.
We have had NC`s raised by our CB related to what they interpret as "EP devices" such as optical inspection sorting equipment , that is integrated into our manufacturing equipment .
My intention and methodology is to exclude these(unless we have added them, as an extra process control for EP purposes) as the list and resulting control plans could be endless , especially when I think about all of the integrated equipment that ensures we manufacture conforming product!.
I will of course include any device outside of the manufacturing equipment that prevents human error, that results in non conforming product.
Just to add, that I have read and understand AIAG CQI-18 Effective Error Proofing and luckily we don`t have any customer CSR`s that require us to be compliant to it as the resources to implement it, would be enormous!.
I would really appreciate your thoughts and perspective on this topic!
Quality Managers for the sites are trying to convince me that IATF requirements for EP does not apply to our industry, as we make billions of products annually, which in my opinion is ridiculous and completely wrong because you cannot just decide to ignore an IATF clause for your own convenience !!.
The processes are many and extremely complex, so my main motivation is to create an EP methodology that works for us and keeps the control plans to a sensible and manageable level.
We have had NC`s raised by our CB related to what they interpret as "EP devices" such as optical inspection sorting equipment , that is integrated into our manufacturing equipment .
My intention and methodology is to exclude these(unless we have added them, as an extra process control for EP purposes) as the list and resulting control plans could be endless , especially when I think about all of the integrated equipment that ensures we manufacture conforming product!.
I will of course include any device outside of the manufacturing equipment that prevents human error, that results in non conforming product.
Just to add, that I have read and understand AIAG CQI-18 Effective Error Proofing and luckily we don`t have any customer CSR`s that require us to be compliant to it as the resources to implement it, would be enormous!.
I would really appreciate your thoughts and perspective on this topic!