Role & responsibilities
Perform routine and stability analysis of pharmaceutical products, raw materials (RM), intermediates, and finished products as per approved specifications and test methods.
Conduct analytical testing using instruments such as HPLC, GC, UV-Visible Spectrophotometer, and other laboratory equipment.
Execute and review stability studies in accordance with ICH guidelines and maintain accurate stability data records.
Investigate and support resolution of Out of Specification (OOS) and Out of Trend (OOT) results through root cause analysis and corrective actions.
Prepare, review, and maintain analytical reports, laboratory notebooks, and documentation in compliance with GMP and regulatory requirements.
Perform calibration, verification, and routine maintenance of analytical instruments.




Ensure compliance with laboratory safety practices, SOPs, data integrity requirements, and quality standards.
Participate in method validation, method transfer, and troubleshooting of analytical methods.
Coordinate with cross-functional teams to support product release and quality objectives.

Preferred candidate profile
B.Pharm, M.Pharm or M.Sc. in Chemistry/Analytical Chemistry or related discipline.
Hands-on experience in HPLC, GC, UV, Stability Testing, RM Analysis, OOS/OOT Investigations, and pharmaceutical QC operations.
Solid understanding of GMP, GLP, data integrity, and regulatory requirements.

📌 Quality Control Executive Telangana (India)
🏢 Aurobindo Pharma
📍 India