QC Chemist

Job Description

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.

Applications are invited from young and dynamic professionals aspiring for a bright career, to join us in the following position:

Major Purpose

• Involve in analysis of raw materials, water samples, in-process and finished products.
• Involve in the analysis of stability samples.
• Prepare reagents and solutions necessary for the analysis & standardize as per procedure.
• Record the analytical results in respective books/ records & complete reports & charts along with samples analyzed.
• Calibrate instruments as per schedule and fill logs.
• Collect and maintain records of retention /control Samples of raw materials, finished products and stability samples as per procedure.
• Revise SOPs and test procedures for raw materials, finished goods and submit for check and approval.
• Revise formats and submit to immediate supervisor for check and approval.
• Participate in the analysis of validation samples.
• Participate in validation of analytical methods.
• Maintain inventory in laboratory with respect to availability of chemicals &reagents, glassware, standard solutions etc.
• Report to immediate supervisor on the daily analysis activities.
• Suggest any ideas for implementation that may help on the improvement of quality system.
• Ensure that the laboratory is maintained clean as per SOP.
• Perform any other activities assigned by the department head from time to time.

Required Number: 2 

Type of Employment: Permanent.

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 Requirement

Education and Experience

• BSc. Degree in Chemistry from a recognized College University 
• Minimum of  2 Year Experience in Supervisor and Related area