Executive- QA (Validation)
Posted Updated
Description
<p style="text-align:center;"><span style="font-size:14px;">1. Preparation and Review of Validation and Qualification related SOP’s.</span></p><p style="text-align:center;"><span style="font-size:14px;">2. Execution and verification of Qualification Activity at the departments levels</span></p><p style="text-align:center;"><span style="font-size:14px;">3. To ensure the preparation and Review of URS/DQ/IQ/OQ/PQ related to all</span></p><p style="text-align:center;"><span style="font-size:14px;">new system and equipment to be installed at the site.</span></p><p style="text-align:center;"><span style="font-size:14px;">4. Preparation and review of Validation and Qualification related Protocols and</span></p><p style="text-align:center;"><span style="font-size:14px;">Reports.</span></p><p style="text-align:center;"><span style="font-size:14px;">5. To investigate, evaluate and conclude the non-conformance / deviation</span></p><p style="text-align:center;"><span style="font-size:14px;">related to validation and qualification.</span></p><p style="text-align:center;"><span style="font-size:14px;">6. To prepare Annual Validation Master Planner and to track and update the</span></p><p style="text-align:center;"><span style="font-size:14px;">same, time to time.</span></p><p style="text-align:center;"><span style="font-size:14px;">7. Issuance and control of Validation and Qualification related documents.</span></p><p style="text-align:center;"><span style="font-size:14px;">8. Preparation, review and execution Cleaning Validation protocol and report.</span></p><p style="text-align:center;"><span style="font-size:14px;">9. Preparation, review and execution Process Validation protocol and report.</span></p><p style="text-align:center;"><span style="font-size:14px;">10. To review the protocols and reports for the Microbiological related testing</span></p><p style="text-align:center;"><span style="font-size:14px;">and Analytical Method validation related activities of QC Laboratory.</span></p><p style="text-align:center;"><span style="font-size:14px;">11. To ensure the allotment of Equipment ID to all new equipment to be</span></p><p style="text-align:center;"><span style="font-size:14px;">installed.</span></p><p style="text-align:center;"><span style="font-size:14px;">12. To ensure the Validation and Calibration Status of the equipment at the Site.</span></p><p style="text-align:center;"><span style="font-size:14px;">13. Preparation of Media Fill Protocols and Reports.</span></p><p style="text-align:center;"><span style="font-size:14px;">14. To participate in Media Fill activities and ensure the review and compliance</span></p><p style="text-align:center;"><span style="font-size:14px;">of the activity as per the Batch Records and Protocols</span></p><p style="text-align:center;"><span style="font-size:14px;">15. To perform any other work as assigned by the Head of department.</span></p>