Master's degree holder in Chemistry with over 9 years of extensive experience in analytical method development for complex injectables.Proficient in operating within development, GMP, and GLP environments.Ability to manage multiple tasks and prioritize assignments independently.Strong written and verbal communication skills enabling effective representation of analytical issues to internal project teams, external contractors, and senior management.Proficient in reviewing quality control documentation, including stability studies, to support drug product manufacturing at contract manufacturing organizations.Known for proactive problem-solving and critical analysis to drive technical and non-technical issue resolutions.