I am revitalizing our QMS (IATF). We are not Design Responsible and note that in our scope.
Practically, I understand the need to apply parts of 8.3 since we are responsible for Process Design.
I would like to know which specific sections of 8.3 that an auditor could legitimately hold us to. Some sections seem obvious and even include 'process design' in the title. Some sections are clearly meant for product design only. The rest seem like a grey zone to me. I would appreciate any direction / feedback .
Practically, I understand the need to apply parts of 8.3 since we are responsible for Process Design.
I would like to know which specific sections of 8.3 that an auditor could legitimately hold us to. Some sections seem obvious and even include 'process design' in the title. Some sections are clearly meant for product design only. The rest seem like a grey zone to me. I would appreciate any direction / feedback .