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)
🏢 Aurobindo Pharma
📍 Telangana