Must have hands on experience on techniques such as HPLC/GC/IC/IR/Titrimetric analysis/wet analysis and troubleshooting during laboratory failures.
Must have exposure to perform Analytical development/ validations/Technology transfer for analytical test methods related to chromatographic and non-chromatographic techniques.
Must be aware about Analytical test method validation requirements from different markets/ respective guidelines, and able to execute protocol-based studies.
Must be aware about quality management system and practices within analytical development and validation lab.
Basic understanding over drug master filing and its process, various modules of dossier.
Exposure to perform laboratory investigation and usage of various investigations tools.
Having interest and theoretical knowledge about spectroscopic techniques such as LCMS/GCMS//NMR is plus