Katie Edwards is a Senior Director of Regulatory Affairs at Quest Diagnostics, a position held since 2025. Previously, Edwards served as a Senior Regulatory Affairs Manager at BD Life Sciences from 2020 to 2021, where a team was managed to support new product development and implement IVDR Class D assay remediation plans. Edwards has extensive experience in regulatory affairs, including roles at Biomeme, Inc. and BD Diagnostics, where they contributed to clinical, quality, and regulatory responsibilities, as well as acted as a technical expert for diagnostic product lines. Edwards holds a Bachelor’s degree in Biology from Villa Julie College and a Master’s degree in Regulatory Science from The Johns Hopkins University.
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