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Officer, QA Validation
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#29912
Remote / WFH
Amneal Pharmaceuticals · 3.3 Hyderabad,
Job Description
Responsible for routine monitoring of Manufacturing Areas.
2 Responsible for the routine GMP Inspection & review of Quality Records of other departments.
3 To monitor and ensure compliance level of organization is as per current GMP requirement
4 Good Documentation recording and updation.
5 Responsible for review of URS, DQ and vendor / suppliers documents related to qualification.
6 Responsible for preparation of Validation / Qualification protocol and report.
7 Responsible for
2 Responsible for the routine GMP Inspection & review of Quality Records of other departments.
3 To monitor and ensure compliance level of organization is as per current GMP requirement
4 Good Documentation recording and updation.
5 Responsible for review of URS, DQ and vendor / suppliers documents related to qualification.
6 Responsible for preparation of Validation / Qualification protocol and report.
7 Responsible for
