Ng2020
Aerospace
- Nov 6, 2020
- 207
Context - I am in a growing startup design/manufacturing environment. No Production Cert.
Note: we do fixed wing airplanes, not rotorcraft - an important distinction because of
27.602/29.602.
Currently our engineering drawings & process specs do not explicitly identify critical parts, nor do they provide direction for manufacturing to conduct specific inspections on such details.
One of our Manufacturing Eng's is from a rotorcraft background and is interested in identifying each critical part in the BOM so that affected work instruction cards get 2x QA signatures.
In your collective experience:
1. is this standard practice in your org.? If so how are critical parts typically identified on the engineering drawings?
This seems like a trivial question, but I don't recall seeing this practice in other organisations. If it was happeneing, it wasn't commonplace or immediately apparent.
2. What are the Manufacturing/ QA implications of such a designation in your organisation ? does this designation purely relate to ensuring serialisation/marking of critical parts under Part 21, or does your organisation impose additional inspection criteria?
Apologies if these questions seem a bit half baked. hopefully this will provoke some good discussion which will yield answers to questions I haven't even thought about yet.
Note: we do fixed wing airplanes, not rotorcraft - an important distinction because of
27.602/29.602.
Currently our engineering drawings & process specs do not explicitly identify critical parts, nor do they provide direction for manufacturing to conduct specific inspections on such details.
One of our Manufacturing Eng's is from a rotorcraft background and is interested in identifying each critical part in the BOM so that affected work instruction cards get 2x QA signatures.
In your collective experience:
1. is this standard practice in your org.? If so how are critical parts typically identified on the engineering drawings?
This seems like a trivial question, but I don't recall seeing this practice in other organisations. If it was happeneing, it wasn't commonplace or immediately apparent.
2. What are the Manufacturing/ QA implications of such a designation in your organisation ? does this designation purely relate to ensuring serialisation/marking of critical parts under Part 21, or does your organisation impose additional inspection criteria?
Apologies if these questions seem a bit half baked. hopefully this will provoke some good discussion which will yield answers to questions I haven't even thought about yet.