We have a procedure on controlling of non-conformance product. As per procedure, for every defect product, QA shall raise defect tag, book defect tag in database and raise SCAR to supplier or internal CAR, then we need to do RCA, CAPA, follow up to close it off. It means for every defect, we need raise CAR/CAPA. Is it practical?
For example, for one time occurred defect in 12 months (cost only $10), short delivery (supplier agree to send missing parts, only one time occurred in 12 months), internal defect (only quick fix) and etc. I don' think it is necessary to raise SCAR/CAR for these non-conformance.
Shall we have "filtering'' system? I.e. all defects shall be booked in database and we monitor them (control chart, Pareto chat and etc.), only critical one to QMS, we need to raise CAR/SCAR. If this is the way, shall we have to define which is critical to QMS in procedure? Please advise. Thanks.
For example, for one time occurred defect in 12 months (cost only $10), short delivery (supplier agree to send missing parts, only one time occurred in 12 months), internal defect (only quick fix) and etc. I don' think it is necessary to raise SCAR/CAR for these non-conformance.
Shall we have "filtering'' system? I.e. all defects shall be booked in database and we monitor them (control chart, Pareto chat and etc.), only critical one to QMS, we need to raise CAR/SCAR. If this is the way, shall we have to define which is critical to QMS in procedure? Please advise. Thanks.