Regulatory Document Coordinator
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Motivated scientist with a breadth of academic, research and professional experience pertaining to pharmaceutical manufacturing and regulatory science. Dedicated to personal and professional growth of self and others.
A highly organized and detail-oriented Regulatory Affairs Specialist with over 4 years of experience ensuring compliance with GMP, FDA, and other regulatory standards in pharmaceutical research and laboratory operations. With expertise includes SOP development, audit preparation, technical documentation, and quality assurance. I have a strong ability to coordinate cross-functional teams and ensure compliance throughout the research and development lifecycle.
A Master of Science in Pharmaceutical Sciences from the University of Georgia in May of 2024
