Pharma QA role as third party Audit/visit of plant

1(Q.M.S) -To check to QA system ,QMS how the plant unit complies cGMP & control on operations.
2(Audit compliance) cross check paper work and work on floor.
3.In process control.
4.lab testing cross checks.
5.Review approve or rejects all things related with compliance/noncompliance with cGMP (e.g.production batch records & release of lots./CAPA related issues.)
6.Update management always informed, example system risk 
,reports of regulatory audits and outcomes and ensure responses from QA end completed after complete varification.
Note:: Dont come in pressure remain independent body being as reviewer approver of process.
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