11 Oct
SEVEN CONSULTANCY
Chennai
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>> JOB DETAILS
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> 1 Review & preparation of MES & other GMP Software Qualification Documents.
> 2 Preparation of URS, GxP Risk Assessment, Qualification protocols (OQ, PQ), RTM, VSR.
> 3 Review URS, RA, Design documents, qualification document.
> 4 Handling of post implementation changes documents.
> 5 Execute OQ and PQ.
> 6 To prepare compliance report for internal / external audit and Compliance of internal/external audit points.
> 7 To Initiation, investigation and evaluation of Change control, CAPA and deviation.
> 8 To prepare & review SOPs.
> 9 To initiate, investigate, lock and closing of TCC, CC, Deviation and Incident report and verify the implemented CAPA and its effectiveness.
> 10 To Prepare PQR/APR.
> 11 Investigation and report preparation of Market Complaints and product failures at shop floor.
> 12 Online review of GMP documents.
> FUNCTIONAL AREA
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> Apply Now
▶️ Quality Assurance Officer -Reputed Medical Device Industry -Chennai, Tamil Nadu, India -4LPA -Pooja
🖊️ SEVEN CONSULTANCY
📍 Chennai