Cadila Pharmaceuticals India is an integrated Healthcare Solutions provider driven by “Passion to innovate to Life”, enjoying more than 70 years of Healthcare heritage worldwide with Regulatory Approvals from USFDA, MHRA, TGA, MCC, and WHO. The company is rapidly expanding its global matrix both in terms of manufacturing facilities and market reach.

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.

Major Purpose

• Ensure BMRs are complete and the necessary data are recorded in PC for PQR

• Follow up of proper documentation of training records.

• Prepare PQR on products produced.

• Prepare/ review BMRs/BPRs for products and submit for approval.

• Revise formats and submit to immediate supervisor for check and approval.

• To collect samples from validation batches at each sampling stages.

• Conduct the necessary test parameters on the samples.

• Ensure that samples of validation batches are submitted/ taken to QC lab. 

• Participate in cleaning validation methods.

• Participate in validation of analytical methods.

• To perform IPQA activities and record results as needed as per the procedure, when assigned/ required.

• Report to immediate supervisor on the daily analysis activities. 

• Compile Report QA activities on weekly and monthly basis.

• To perform any other activities assigned by the department head from time to time.

• Suggest any ideas for implementation that may help on the improvement of quality system.

Salary and Other Benefit Packages: Attractive and can be determined with negotiation based on the candidate’s previous earning, qualification and competency.

Work Place: Gelan Factory

Job Requirements

Education and Experience

• BSc. Degree in Pharmacist from a recognized College University 

• Minimum of 2 Year Experience in Supervisor and Related area

  Skills 

• Excellent oral and written communication skill.

• Strong analytical and problem solving skill.

• Basic knowledge of MS Office, words, excel, internet etc. 

• Willingness to learn, improve and adapt to changing requirements.

How to Apply

Interested and qualified applicants can apply online using THIS LINK