Margreta Baeva, Ms Email & Phone Number

I am a quality-driven and result-oriented professional with more than 15 years of pharmaceutical industry experience, working in a GMP regulated environment, supporting development, manufacturing, validation, testing and submissions of solid and liquid dosage formulations. Expertise in analytical method development / validation / verification / remediation and transfer of DP, API and inactive ingredients. Experience in leading R&D analytical projects, GMP release, stability testing, and conducting of laboratory investigations. Known for talent development, management, and mentoring. Recognized for collaborating and communicating with senior management, cross-functional teams, and direct reports. Capable of handling multiple assignments with changing priorities. Possess extensive training and experience utilizing various analytical techniques including HPLC, UPLC, GC, GC/HS, KF, dissolution, spectroscopy, etc.

Listed skills include Cmc Audit, Training Program Development, R&D Stability Program Management, Method Validation Gap Assessment, and 28 others.