Officer - QC Analytical

About the role

The QC Analytical Officer is responsible for performing stability and finished‑product testing in a pharmaceutical environment, ensuring that all analytical activities comply with regulatory standards and internal quality policies.

Key responsibilities

• Analyze stability and finished‑product samples and compile reports following ALCOA principles.
• Maintain and operate laboratory instruments such as dissolution testers, UV spectrophotometers, analytical balances, pH meters and sonicators.
• Ensure data integrity and Good Documentation Practice (GDP) compliance throughout all activities.
• Manage the stability chamber and associated tracking system, including charging and withdrawal of samples per approved protocols.
• Perform routine instrument maintenance and calibration to guarantee reliable performance.

Required profile

• B.Pharm, M.Sc. or M.Pharm degree.
• 2 to 4 years of experience in pharmaceutical quality control or analytical laboratories.

Required skills

• Stability testing and sample handling.
• ALCOA‑compliant report preparation.
• Operation and maintenance of dissolution testers, UV spectrophotometers, analytical balances, pH meters and sonicators.
• Data integrity management and GDP adherence.
• Stability chamber operation and sample tracking.