Assistant Manager QA

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   Reporting to (Designation) : Manager QA / QC Responsibilities: Ensure equipment’s have appropriate documents.  Ensure that all instruments/ equipment’s have the necessary current revised SOP.  Ensure that the instruments are calibrated as per schedule and the necessary schedules are maintained.  Training to the staff.   Train manufacturing staff on different GMP issues.   Ensure that training records are adequately maintained.  Prepare and revise documents.   Prepare and revise formats being used in the factory.   Arrange internal audits of the company to be carried out by the department.   Ensure that compliance reports from departments are documented.    Handle customer complaints and recall procedure, when encountered.   Review and check all the reports being generated in the QA and QC Department.   Review on any OOSs encountered and ensure that they are recorded  Handling of change control.  Handling deviation. Preparation/ revision of SOPs.  Preparation or revision product quality review. Handling validation Handling self-inspection.  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