When certificates, purchase orders, batches and technical specifications are held in separate sources, their fields must be matched by hand before a list of document discrepancies can be prepared.
The incoming quality specialist must compare every suggestion in the document discrepancy list with its source record; missing or conflicting evidence must not replace the final decision.
If an approved deviation permit or equivalent document code is not set aside for review, nonconforming material could be accepted or a conforming batch could be held; the record must not proceed without a human decision.
The incoming quality specialist compares the document discrepancy list with the supporting record. The workflow pauses when an approved deviation permit or equivalent document code exists. The responsible person can revise or reject the suggestion, or request further information.
Only the fields required for this decision should be processed from the certificate, purchase order, batch and technical specification. Access to the source systems must be authorised separately from the incoming quality specialist role, and personal data, commercial information and technical secrets must not be passed into the model context unnecessarily. Reading, suggestions and human decisions must be logged separately.
A good fit
Not a good fit
Certificates, purchase orders, batches and technical specifications can be received through an API or controlled file transfer. Fields whose source and version cannot be established are not treated as confirmed information.
The record goes to the incoming quality specialist for review when an approved deviation permit or equivalent document code exists. If supporting evidence is missing, no action is taken in the target system.
No. The document discrepancy list remains a draft until the incoming quality specialist approves it. Acceptance, revision and rejection are recorded in the processing log as human decisions.
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