1. Chemical analysis of Solid (Tablet Granules, Capsules), Cream, Gels, Sterile Products (Antibiotics, Injections, Infusions) and Liquid Dosage Forms (Syrups, Suspensions). 

2. Managing testing and preparing all documentation related to new molecules, managing their stability and getting it inspected from DRAP.

3. Testing of raw materials.

3. Regulatory work (Dossier Formulation, Reviewing.

4. Stability testing of Products according to stability plan.

5. Water Analysis of the site water and also the water used in formulation and WFI.

6. Reagents Preparation & Standardization to ensure accuracy of results.

7. Review laboratory notebooks and raw data for correction and accuracy.

8. Physical testing of finished products.

9. In process control of new product/ Batch in Packaging and Manufacturing Areas in Production.

10. QA Documentation and Paper Work.

11. Documentation for Export Products.

Working on SOP (making, updating and implementation).

12. Document auditing.

13. Manage and maintain Data bases for the Quality system.