Job Description
Key Responsibilities:
Develop and validate analytical methods for drug substances and drug products
Handle techniques like HPLC, GC, UV, IR, Dissolution, etc.
Perform method transfer to QC/plant locations
Prepare protocols, reports, and documentation as per regulatory guidelines
Support stability studies and impurity profiling
Ensure compliance with GLP, cGMP, and data integrity norms
Troubleshoot analytical issues during development and commercial stages
Work closely with R&D, QA, and manufacturing teams