
Detail-oriented and results-driven potential quality, validation or manufacturing engineer with a strong foundation in manufacturing processes and GMP compliance. Skilled in developing and executing over 10+ process validations, including sterile filling, mechanical and process flow optimization as well as cleaning/organizational laboratory studies. Experienced in supporting and performing IQ, OQ, PQ protocols, analyzing validation data, and reviewing technical documentation to ensure regulatory alignment. Known for excellent communication, collaboration, organization, and project management skills, with proficiency in Microsoft Office and statistical analysis tools. Committed to ensuring process reliability, quality, and continuous improvement in a regulated environment. Willing and eagerness to learn and develop skills that can help transfer over to any engineering position.