TS16949:2009 or TS16949E specifically states under 8.2.2.4 the following note:
NOTE Specific checklists should be used for each audit.
Please explain how everyone is saying checklists are banned or not to be used.
My problem with what was here for internal audits upon my arrival with a new company was that the checklists were not controlled, never changed, they were however specific to each department and the directives or procedures that applied to the particular department, however it was stale and did not help improve anything. It was merely used to remind everyone how horrible the document control process was, nothing more.
I am trying to further develop a process based plan, guide and notes document that I originally found as a checklist sort of thing on this very forum posted by Antonio Santos.
I want the document to serve as the template for each internal audit that will satisfy ISO9001:2008, AS9100C and TS16949E requirements all in one. Antonio's design was not really a checklist it was more of a diagram, matrix and notes multi-tabbed document that required the auditor to interact with all of the necessary inputs, outputs and support processes.
I really liked his approach and will continue to modify the document and the process it will control until I can get it to meet the requirements for all 3 QMS standards independently, I do not want 3 different audit programs. I will also ensure it requires the use of the latest Quality Manual as that will also provide up to date requirements, process and procedure linkage, etc.
I have attached a copy of what i have at this very moment, of what was origjnally Antonio's design, however it is nowhere near complete in my opnion, not for my needs, not yet.
NOTE Specific checklists should be used for each audit.
Please explain how everyone is saying checklists are banned or not to be used.
My problem with what was here for internal audits upon my arrival with a new company was that the checklists were not controlled, never changed, they were however specific to each department and the directives or procedures that applied to the particular department, however it was stale and did not help improve anything. It was merely used to remind everyone how horrible the document control process was, nothing more.
I am trying to further develop a process based plan, guide and notes document that I originally found as a checklist sort of thing on this very forum posted by Antonio Santos.
I want the document to serve as the template for each internal audit that will satisfy ISO9001:2008, AS9100C and TS16949E requirements all in one. Antonio's design was not really a checklist it was more of a diagram, matrix and notes multi-tabbed document that required the auditor to interact with all of the necessary inputs, outputs and support processes.
I really liked his approach and will continue to modify the document and the process it will control until I can get it to meet the requirements for all 3 QMS standards independently, I do not want 3 different audit programs. I will also ensure it requires the use of the latest Quality Manual as that will also provide up to date requirements, process and procedure linkage, etc.
I have attached a copy of what i have at this very moment, of what was origjnally Antonio's design, however it is nowhere near complete in my opnion, not for my needs, not yet.