I am an accomplished professional delivering over 3 decades of career success in the Pharmaceutical industry, specializing in small molecule research and development.

My dexterity lies in operational governance, process improvement, project management, and analytical development within R&D, contributing to the successful implementation of various interventions and initiatives. Demonstrated excellence in spearheading the QC lab functions, method introduction & set-up, calibrations & routine PM of lab equipment with regular audit (internal and external).

Over the time, I have proved my excellence in wide range of technical areas, including analytical method development and validation, quality control, GMP compliance, regulatory affairs, project management, risk assessment, and process improvement.

Achieved a notable accomplishment in the current role by implementing amongst various processes, the stage gate process for new product development, resulting in a significant reduction in development timelines and increased productivity.

I have mastered the administration of supervising QC work & documentation as per pharmaceutical industry regulations & various other regulatory authorities such as USFDA, TGA, WHO, MCC, MHRA, ANVISA and PMDA