Bachelor’s degree in pharmacy, chemistry, chemical engineering or any related field
Minimum -9-6 years in quality control laboratories in the pharmaceutical industries
لشغل المهام التالية:
Supervision of quality control, review the testing reports for the related analysis and arrange the responsibilities of the analysts to test the raw materials and finished products.
1. Perform the sampling and analysis process for raw and packaging materials as per related methods.
3. Prepare the standards and solution required in the analysis process as per the SOPs.
4. Record all the analysis process in the related documents as per approved SOPs.
5. Follow the safety precautions in the laboratory.
6. Participate and involved in the calibration of the laboratory instruments.
7. Participate and involved in the process and cleaning validation studies.
8. Perform the sampling and analysis process for the finished and bulk products as per related methods.
9. Perform any orders within the responsibility from the manager.
10. Perform the analysis process for stability and analytical method validation studies as per related methods.
11. Inform the manager for any out of specification results.
12. Ensure the implementation the training plans for the employees.
13. Follow up the analysis of water samples from the water treatment loop.
14. Participate and follow the stability study.
15. Arrange the responsibilities of the analysts to test the raw materials and finished products
16. Ensure the effectiveness of the documentation system with the laboratory.
17. Review the testing reports for the related analysis.
18. Prepare and update the analysis method as per the standard pharmacopeia.
19. Review and update the related documents such as (SOPs, forms, and records).
20. Follow up the chemical stock and inform the Manager for any shortage.
By admin 
Minimum -9-6 years in quality control laboratories in the pharmaceutical industries
لشغل المهام التالية:
Supervision of quality control, review the testing reports for the related analysis and arrange the responsibilities of the analysts to test the raw materials and finished products.
1. Perform the sampling and analysis process for raw and packaging materials as per related methods.
3. Prepare the standards and solution required in the analysis process as per the SOPs.
4. Record all the analysis process in the related documents as per approved SOPs.
5. Follow the safety precautions in the laboratory.
6. Participate and involved in the calibration of the laboratory instruments.
7. Participate and involved in the process and cleaning validation studies.
8. Perform the sampling and analysis process for the finished and bulk products as per related methods.
9. Perform any orders within the responsibility from the manager.
10. Perform the analysis process for stability and analytical method validation studies as per related methods.
11. Inform the manager for any out of specification results.
12. Ensure the implementation the training plans for the employees.
13. Follow up the analysis of water samples from the water treatment loop.
14. Participate and follow the stability study.
15. Arrange the responsibilities of the analysts to test the raw materials and finished products
16. Ensure the effectiveness of the documentation system with the laboratory.
17. Review the testing reports for the related analysis.
18. Prepare and update the analysis method as per the standard pharmacopeia.
19. Review and update the related documents such as (SOPs, forms, and records).
20. Follow up the chemical stock and inform the Manager for any shortage.
Job@doxpharma.com.sa