QC Analytical Officer

About the role

The QC Analytical Officer is responsible for performing stability and finished‑product testing, ensuring accurate reporting, and maintaining analytical instruments in a pharmaceutical environment. The role supports compliance with data integrity and Good Distribution Practice (GDP) standards.

Key responsibilities

• Analyze stability and finished‑product samples and compile reports following ALCOA procedures.
• Test miscellaneous samples and generate corresponding analytical reports.
• Maintain and calibrate instruments such as dissolution testers, UV spectrophotometers, analytical balances, pH meters, and sonicators.
• Ensure data integrity policies and GDP compliance are consistently applied.
• Manage stability chambers, trackers, and oversee charging and withdrawal of stability samples according to approved protocols.

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

• Dissolution testing equipment operation.
• UV spectrophotometer usage.
• Analytical balance handling.
• pH meter measurement.
• Sonicator operation.
• Knowledge of ALCOA reporting standards.
• Understanding of data integrity and GDP compliance.