QC Chemist (Formulation)

 Key Responsibilities:

• Perform analysis and testing of Raw Materials (RM), Packaging Materials (PM), in-process samples, finished products, and stability samples as per pharmacopoeia standards.
• Operate, calibrate, and maintain analytical instruments such as HPLC, GC, UV, IR, Dissolution Apparatus, etc.
• Ensure timely release of materials/products with accurate and complete documentation.
• Maintain records, calibration logs, data integrity, and adherence to SOPs.
• Follow cGMP, GLP, and regulatory compliance in the QC laboratory.
• Handle OOS / OOT results, deviations, lab incidents, and prepare required reports.
• Prepare and review STPs, COA, specifications, and test reports.
• Coordinate with QA, Production, and Warehouse teams to ensure smooth operations and timely batch release.
• Support internal and external audits such as WHO / USFDA / MHRA / etc.

Requirements:

• B.Sc./M.Sc. Chemistry or B.Pharm/M.Pharm.
• Hands-on experience in RM/PM analysis (3–6 years).
• Knowledge of pharma guidelines (IP, BP, USP).
• Strong documentation and compliance skills.
• QC: 1.5 year (Preferred)

Why Join Us?

• Exposure to regulated pharma environment.
• Professional growth in a leading formulation company.
• Supportive work culture with career stability.