Summary
Highly accomplished Validation Engineer with 6 years of experience specializing in GxP environments within the biopharmaceutical and medical device industries. Proven expertise in developing and executing comprehensive qualification protocols (IQ, OQ, PQ) for critical equipment, facilities, utilities, and software systems. Adept at ensuring compliance with FDA regulations, EU Annex 11, and company standards, consistently delivering projects on time and within budget. Seeking to leverage strong analytical skills and a meticulous approach to validation to contribute to innovative manufacturing processes.




