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