Develop, optimize, and validate analytical methods for NCEs and generic compounds using HPLC-UV
Ensure methods meet regulatory requirements
Perform dose verification analysis on preclinical dose formulation samples using HPLC-UV, GC, and
Generate Certificates of Analysis (CoA) for IND submissions
Conduct routine calibration and maintenance of laboratory equipment (HPLC systems, pH meters
Maintain calibration records and ensure instruments remain in operating parameters

🎯 Requirements

Master's degree (M.Sc. or M. Pharm.) in Chemistry, Pharmaceutical Sciences, or related discipline
Minimum 3-4 years of professional experience in analytical chemistry, pharmaceutical formulation
Expertise in HPLC-UV, GC, LC-MS/MS, and ICP-MS
Knowledge of GLP and GMP guidelines
Proficiency in analytical method development, validation, and documentation
Technical competency in data management and regulatory documentation

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