Kimberly Y. Dayot

I'm a dedicated Document Control professional with over 5 years of experience in pharmaceutical quality assurance and regulatory compliance. I specialize in managing complex document workflows while ensuring FDA compliance in fast-paced production environments.

My expertise lies in process improvement and cross-functional collaboration, having successfully managed approximately 720 documents annually while working closely with Manufacturing, Quality Control, and R&D teams.

I'm passionate about leveraging technology to streamline document management processes and have received recognition for my exceptional support of Technical Operations teams.