Job Responsibilities:
1. Responsible for implementation of cGMP in the plant.
2. Responsible for preparation & review of Protocols and Reports.
3. Responsible for preparation of Quality Documents such as VMP.
4. Responsible for the Preparation of Planners such as calibration, VMP planner etc.
5. Responsible for the Verification and participation in the execution of Validation and Qualification activities of equipment, instrument, utility, process etc.
6. Responsible for Preparation, Review of Qualification Protocols and Reports.
7. Responsible for issuance, and control of drawing layouts.
8. Responsible for the allocation of equipment, instrument, facility, documents numbering.
9. Responsible for review of Specifications, Stability Protocols and reports.
10. Responsible for Document Storage and retention.
11. Should have knowledge on cleaning validation and computer system validation (CSV)
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