Sr. Qc Officer

Tabuk Pharmaceuticals Manufacturing Co

1. Follow approved departmental SOPs.

2. Follow cGMP, GDPs and GLPs.

3. Follow all safety precautions as per EHS SOPs.

4. Sampling, analysis and reporting for stability samples.

5. To follow proper disposable of laboratory waste, samples after analysis.

6. To handle carefully sophisticated instruments (e.g. HPLC, UV, ICP and Dissolution tester) and other instruments.

7. To maintain sanitation, cleaning and housekeeping in the department.

8. To Maintain inventory of standards, chemicals etc. and updating lab requirement.

9. Preparation and standardization of volumetric solutions, test solution and documentation.

10. To follow approved specification and test procedures for analysis.

11. Perform testing for all materials/products.

12. To record analytical results in the respective logbook and confirm the calculations.

13. To perform calibration of the QC instruments as needed.

14. To perform verification for QC balances as needed.

15. To prepare stability COAs.

16. Follow the documentation system requirements.

17. To investigate and reporting of Out of Specification/Trend (OOS)/OOT results if any.

18. To prepare stability summary and maintain stability trend as per set norms.

19. To perform standardization against Reference standard as per valid approved test procedure.

20. Report to supervisor for any deviation from set norms.

21. Work with supervisor to develop the test plan scope, coverage and objectives.