Senior Quality Control Officer
Tabuk Pharmaceuticals
Saudi Arabia
On-site
SAR 120,000 - 150,000
Full time
Responsibilities
- 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.