QC Analytical Officer

About the role

The QC Analytical Officer is responsible for performing stability and finished‑product analyses in a pharmaceutical laboratory, ensuring that all results are documented according to ALCOA principles and regulatory standards.

Key responsibilities

• Analyze stability and finished‑product samples and compile detailed reports following ALCOA procedures.
• Conduct testing on miscellaneous samples and generate corresponding documentation.
• Maintain and calibrate laboratory instruments such as dissolution testers, UV spectrophotometers, balances, pH meters, and sonicators.
• Ensure compliance with data‑integrity policies and Good Distribution Practice (GDP) requirements.
• Operate and monitor stability chambers and associated tracking systems.
• Manage the 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 testing.

Required skills

• Proficiency with dissolution testing apparatus.
• Experience using UV spectrophotometers.
• Ability to operate analytical balances, pH meters and sonicators.
• Knowledge of ALCOA documentation standards and GDP compliance.

What we offer

• Opportunity to work in a regulated pharmaceutical environment.
• Access to modern analytical instrumentation.
• Professional development in quality control and compliance.