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Kimberley Low is a skilled professional in regulatory affairs with extensive experience in managing regulatory databases and compliance processes within the medical device industry. Currently serving as a Senior Regulatory Affairs Process Specialist at Cepheid, Kimberley oversees multiple regulatory databases and leads continuous improvement projects, including the formal validation of TrackWise Software. Previously at Dexcom, Kimberley played a pivotal role in designing a new Regulatory Affairs Database and was involved in international regulatory compliance efforts. Additional roles at Dexcom included coordinating regulatory submissions and supervising a team focused on customer advocacy. Kimberley also gained valuable laboratory experience through various assistant roles at UCSD, further strengthening a background in microbiology earned from a Bachelor's degree at the institution.