1. Preparation and review of Standard Operating Procedures.
2. Issuance, review of OOS,OOT,Deviation,CAPA,Change Control & its Management.
3. Handling and monitoring of control samples.
4. To impart internal trainings to DCAL Employees.
5. Review of Calibration records, Instrument Logs of Quality Control.
6. To Review of Analytical Method Validation protocols and reports.
7. Review of the Instrument qualifications and re-qualifications protocols of
Quality control.
8. Preparation & review of quality risk assessment documents.
9. Review and approval of analytical data related to QA release.
10. Review & Approval of Specification STP, Raw data sheet etc.
11. To review laboratory investigations related to complaints and deviations
and to ensure CAPA related to QC are completed within timeline.
12. Internal Audit and External audit Compliance
13. To support RA for analytical assistance.
14. Review of working standard management and Stability studies.
15. Handling of customer complaint, OOS, OOT, Incidents, Deviation & CAPA .
16. Responsible and participation, review of OOS Investigation, Deviation,
Complaint Investigation.
17. To carry out any job assigned by Immediate Supervisor/HOD based on
training.
18. To maintain safety, health and setting norms and usage of personal
protective equipment during work.