MadMango
Mechanical
- May 1, 2001
- 6,992
Hello all, I have an ISO9001:2000 auditing problem I would like to present here for discussion.
I moved away from the medical field that dealt with FDA, GMP and ISO9001:2000 to the manufacturing industry. This company has been ISO9001:1994 registered in the past, and has also been registered ISO9001:2000. I’ve been at this company for about 3 years now, and have been involved with their ISO program for about 2 years, and am now a lead internal auditor.
For the life of me, I can’t see how this company became registered at all. It seems that management does not take the registration seriously even though they continue to praise the system in allowing us to be competitive in the market place. Every time I try to schedule audits with various departments, the managers blow-off the need. Whenever I try to raise these issues to the QMR or others in top management the issues seem to stop in their tracks, not going anywhere.
As an example, I have completed an audit discrepancy report (ADR) about not being able to schedule for an audit, under Section 6.1 Resource Management, Provision of Resources in that I can’t get anyone to meet with me to conduct internal audits. After I submit the ADR, the QMR just signs it off, saying he’s spoke to that particular manager about having to support us, blah, blah, blah... I still haven't been able to schedule an internal audit.
I don’t want to “shaft” my employer by allowing them to loose their certification, but at the same time, if no one wants to take it seriously, I shouldn’t be wasting my time with it either. Now my question: have any of you internal auditors been in similar situations, and if so, what course of action did you take, and what was the final outcome?
PS- thanks for letting me vent a bit.
Ray Reynolds
"Computers in the future may weigh no more than 1.5 tons."
Popular Mechanics, forecasting the relentless march of science, 1949
Have you read faq731-376 to make the best use of Eng-Tips Forums?
I moved away from the medical field that dealt with FDA, GMP and ISO9001:2000 to the manufacturing industry. This company has been ISO9001:1994 registered in the past, and has also been registered ISO9001:2000. I’ve been at this company for about 3 years now, and have been involved with their ISO program for about 2 years, and am now a lead internal auditor.
For the life of me, I can’t see how this company became registered at all. It seems that management does not take the registration seriously even though they continue to praise the system in allowing us to be competitive in the market place. Every time I try to schedule audits with various departments, the managers blow-off the need. Whenever I try to raise these issues to the QMR or others in top management the issues seem to stop in their tracks, not going anywhere.
As an example, I have completed an audit discrepancy report (ADR) about not being able to schedule for an audit, under Section 6.1 Resource Management, Provision of Resources in that I can’t get anyone to meet with me to conduct internal audits. After I submit the ADR, the QMR just signs it off, saying he’s spoke to that particular manager about having to support us, blah, blah, blah... I still haven't been able to schedule an internal audit.
I don’t want to “shaft” my employer by allowing them to loose their certification, but at the same time, if no one wants to take it seriously, I shouldn’t be wasting my time with it either. Now my question: have any of you internal auditors been in similar situations, and if so, what course of action did you take, and what was the final outcome?
PS- thanks for letting me vent a bit.
Ray Reynolds
"Computers in the future may weigh no more than 1.5 tons."
Popular Mechanics, forecasting the relentless march of science, 1949
Have you read faq731-376 to make the best use of Eng-Tips Forums?