M
Marilyn
I need help in understanding how recent organizational and reporting structure changes at our company will comply with ISO requirements on maintaining independence for quality verification activities and internal auditing.
Last week, our President announced that the Quality Managers will now dually report to the Plant Manager and also to the Quality Director. He also stated that if the Quality Manager and the Plant Manager don't agree on issues (product acceptance, disciplinary actions, vacations, etc), the Plant Manager and the Quality Director then will have to reach a decision. The major concern is, of course, product acceptance through QA functions. I might also state that the Plant Managers at each facility are fully hands on and are responsible for ensuring product delivery. They are at a level immediately above the Production Foor Supervisor/Mold Techs.
What does ISO state in regard to a reporting structure where the Quality Director doesn't have the final call on acceptable product and does not have full responsibility for the Quality Dept.? And also with the Quality Department reporting to Production, how does that obviously affect internal auditing? In looking at the 1994 standard, it appears that there is a conflict in 4.1.2.1 on organization freedom and authority and also in 4.1.2.2 verification resources. I need guidance on whether we can be complaint.
Thanks!
Marilyn
Last week, our President announced that the Quality Managers will now dually report to the Plant Manager and also to the Quality Director. He also stated that if the Quality Manager and the Plant Manager don't agree on issues (product acceptance, disciplinary actions, vacations, etc), the Plant Manager and the Quality Director then will have to reach a decision. The major concern is, of course, product acceptance through QA functions. I might also state that the Plant Managers at each facility are fully hands on and are responsible for ensuring product delivery. They are at a level immediately above the Production Foor Supervisor/Mold Techs.
What does ISO state in regard to a reporting structure where the Quality Director doesn't have the final call on acceptable product and does not have full responsibility for the Quality Dept.? And also with the Quality Department reporting to Production, how does that obviously affect internal auditing? In looking at the 1994 standard, it appears that there is a conflict in 4.1.2.1 on organization freedom and authority and also in 4.1.2.2 verification resources. I need guidance on whether we can be complaint.
Thanks!
Marilyn