API & impurity reference standard management.OOS investigations of API & drug products - identification of unknown impurities.Complex impurity synthesis.Process development & scale-up of NCEs.

Provide global support for API & impurity reference standards - lifecycle management, which includes supply of impurity standards to R&Ds, major manufacturing locations and API customers. OOS investigations for API and drug products to identify unknown impurities. Synthesis of process & degradation impurities, purification & characterization to prepare reference standards. Process development of NCEs - Optimization, scale-up of NCE molecules from lab scale to kilogram… Show more Provide global support for API & impurity reference standards - lifecycle management, which includes supply of impurity standards to R&Ds, major manufacturing locations and API customers. OOS investigations for API and drug products to identify unknown impurities. Synthesis of process & degradation impurities, purification & characterization to prepare reference standards. Process development of NCEs - Optimization, scale-up of NCE molecules from lab scale to kilogram scale & regulatory filing support for the same. Show less

To collaborate successfully with both internal and external colleagues to achieve difficult company objectives.

Proactive management style characterized by effective leadership, commitment, enthusiasm, communication and great teamwork

Lead scientists to the highest level of scientific excellence and productivity in the creation of API synthetic processes

Demonstrated success in transferring R&D API processes into production

Identify and implement technologies to expedite the API process.Guide and mentor the development team to develop small molecule generic APIs for regulated markets.

Basics of technology transfer Costing of API process developed

Learning of API process development for large scale manufacturing.Robust, green & cost effective process for APIs.