Officer

About the role

The Quality Control Officer will be responsible for performing routine and stability analysis of Active Pharmaceutical Ingredients (APIs) using analytical instruments such as HPLC and GC while ensuring compliance with current Good Manufacturing Practices (cGMP), Good Laboratory Practices (GLP), and regulatory requirements.

What you'll do

• Perform routine, in-process, raw material, finished product, stability, and cleaning validation sample analysis using HPLC and GC
• Execute analytical testing as per approved specifications, test methods, SOPs, and pharmacopoeial requirements
• Prepare and standardize reagents, volumetric solutions, and reference standards
• Review analytical data, chromatograms, calculations, and test results for accuracy and compliance
• Maintain laboratory documentation, including analytical worksheets, logbooks, instrument usage records, and electronic data in accordance with ALCOA+ principles

What you need

• 2–5 yrs of experience
• HPLC
• GMP
• GLP
• Documentation
• Quality control
• Chemistry
• M.Sc

Good to have

• SOP writing