Walk-in || Quality Control Executive

Job description

**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. - Strong understanding of GMP, GLP, data integrity, and regulatory requirements.