Jr. QA Pharmacist

Cadila Pharmaceuticals (Ethiopia) P.L.C, a Joint Venture Company between Cadila Pharmaceuticals Limited, India and Almeta Impex P.L.C, Ethiopia, put up a Pharmaceuticals Manufacturing facility for Tablets, Capsules & Liquids at Akaki, near Addis Ababa. The aforementioned Plant is one of its kind in Ethiopia and the first Pharmaceutical Formulation Manufacturing Plant of the country to receive Certificate of PICS – Conformity in 2011 as per EU guidelines, to comply with the WHO-led regulatory requirements of Good Manufacturing Practice (GMP) & also received cGMP certificate Ethiopian Food & Drug Authority.

Cadila Pharmaceuticals (Ethiopia) PLC has set an aggressive growth plan to meet the needs of the people of Ethiopia for high-quality Medicines at affordable prices by expanding the reach across Ethiopia. To fulfill our long-term vision and objectives, we need young people to work with us in the following vacant posts

Reporting to (Designation): QA Manager

Department / Section: QA

Responsibilities:

1. Ensure BMRs are complete and the necessary data are recorded in PC for PQR
2. Follow up of proper documentation of training records.
3. Prepare PQR on products produced.
4. Prepare/ review BMRs/BPRs for products and submit for approval.
5. Revise formats and submit to immediate supervisor for check and approval.
6. To collect samples from validation batches at each sampling stages.
7. Conduct the necessary test parameters on the samples.
8. Ensure that samples of validation batches are submitted/ taken to QC lab.
9. Participate in cleaning validation methods.
10. Participate in validation of analytical methods.
11. To perform IPQA activities and record results as needed as per the procedure, when assigned/ required.
12. Report to immediate supervisor on the daily analysis activities.
13. Compile Report QA activities on weekly and monthly basis.
14. To perform any other activities assigned by the department head from time to time.
15. Suggest any ideas for implementation that may help on the improvement of quality system

1. Maintain records
2. Revise documents
3. Participate in validation activities
4. Perform IPQA activities
5. Any other activities