I audit different processes to make sure that Auditees are doing what they say (written procedure) they do. At the planning stage, I look at their procedures, take note of their required records and go over the overall process requirements and develop my checklist. I take note outstanding issues, previous audit results, CARs and check on CA status. I audit from the end product and backwards, go the trail of how the end product was manufactured.
I am only doing audits based on what is assigned to me by the Management Rep.
If I miss something please or if there are areas for improvement please let me know.
Risk planning, I think I am behind with this one.
Hi Chance,
I think you are considering to audit for process approach.
I do not know if you verify the effectiveness ( and the efficiency) of your QMS processes during your internal audit program , in addition to the compliance to the internal procedures as well as versus ISO 9001 and customer requirements.
Rather than using check list, you could adopt turtle diagrams to assess QMS processes and report results to management review in terms of major issues and opportunity for improvement to raise the bar of your entire QMS, aiming at continual improvement.
In addition to internal procedures and ISO 9001, you could also rfers to ISO 9004 for continual improvement. It is not a mandatory norm but an useful guidelines to pursue improvement of an organization.
As further advice, you would also like to advice to work in strict contact with top mgmt and processes owners in order to modify or add other audit to your program in case of major internal issue as well as CAR or return material for your customer.
See you and good luck