Your mission
Method Development and Quality Control:
- Develop and validate analytical methods for impurity, purity, and identity analysis using techniques such as UV-Vis, NMR, HPLC, GC, and Raman spectroscopy.
- Establish robust processes for stability testing and impurity profiling for drug substances, intermediates, and final products.
- Provide analytical support for manufacturing development and toxicology studies, including analysis of in-house produced samples and impurities synthesised for evaluation.
- Collaborate with multidisciplinary teams, including R&D, product development, and regulatory teams, to align analytical processes with project goals.
- Write protocols, technical reports, and data summaries, ensuring full compliance with GMP/GLP standards.
- Contribute to regulatory submissions.