K
kjoberk
I looked through the NC and CA forum, but couldn't find anything about the exact question I have. A little background:
My company has been ISO certified for about 7 years. We are currently AS9110 certified.
During our ISO only stage (before my time at the company), any "nonconformance" was directly turned into a Corrective Action. It didn't matter what it was, it was automatically elevated to a CA. We went through the whole process...identify the issue, investigate and do a root cause analysis, develop a corrective action, implement and monitor/verify, then close the CA.
For our AS cert, we had to come up with an NCR form and follow our procedure (that admittedly, we had written but never used previous to AS).
We currently have two separate processes for our NCR and our CA.
Our (my boss's) issue and concern with the NCR is he doesn't fully understand how to separate out the two. It *feels* like when I'm doing NCR's, I'm doing a CA anyway. Our NCR form has a section for discrepancies or deviations, a section for findings/notes, and then a comments section. Which, to me, all feels very similar to a CA. Do the investigation, figure out what happened, find a solution. The only difference is that a CA will contain a root cause and a statistical analysis (if warranted on the statistical thing), but, I've written root causes in our NCRs too.
So I guess my question is, how do we make this system work for us? We're taking any issue we have an saying its a nonconformance. Some of them, depending on the severity of the issue or the risk of it continuing, get elevated instantly, while others seem kind of in limbo.
Does anyone have examples of what their criteria for an NCR vs a CA is? Or what I'm doing wrong?
I was thinking of suggesting that we use NCRs specifically for our repair/refurbishment side of our company (we are a helicopter maintenance company) and then CA's for everything else. I have no idea. I'm racking my brain....I want to give my boss something that will be more helpful than what we're currently doing.
My company has been ISO certified for about 7 years. We are currently AS9110 certified.
During our ISO only stage (before my time at the company), any "nonconformance" was directly turned into a Corrective Action. It didn't matter what it was, it was automatically elevated to a CA. We went through the whole process...identify the issue, investigate and do a root cause analysis, develop a corrective action, implement and monitor/verify, then close the CA.
For our AS cert, we had to come up with an NCR form and follow our procedure (that admittedly, we had written but never used previous to AS).
We currently have two separate processes for our NCR and our CA.
Our (my boss's) issue and concern with the NCR is he doesn't fully understand how to separate out the two. It *feels* like when I'm doing NCR's, I'm doing a CA anyway. Our NCR form has a section for discrepancies or deviations, a section for findings/notes, and then a comments section. Which, to me, all feels very similar to a CA. Do the investigation, figure out what happened, find a solution. The only difference is that a CA will contain a root cause and a statistical analysis (if warranted on the statistical thing), but, I've written root causes in our NCRs too.
So I guess my question is, how do we make this system work for us? We're taking any issue we have an saying its a nonconformance. Some of them, depending on the severity of the issue or the risk of it continuing, get elevated instantly, while others seem kind of in limbo.
Does anyone have examples of what their criteria for an NCR vs a CA is? Or what I'm doing wrong?
I was thinking of suggesting that we use NCRs specifically for our repair/refurbishment side of our company (we are a helicopter maintenance company) and then CA's for everything else. I have no idea. I'm racking my brain....I want to give my boss something that will be more helpful than what we're currently doing.