Our Team

Rebecca joined Biologics Consulting in April 2026 and has over 13 years of experience in the medical device and biopharmaceutical industry, including seven years managing quality operations for contract testing laboratories and contract manufacturing facilities. Rebecca also has experience in authoring IND and BLA sections as well as supporting 510k submissions.

Rebecca previously worked at Iovance Biotherapeutics, Inc. as a lead scientist for analytical development and transitioned to quality control management for external operations. Rebecca served as the quality point of contact for qualification and phase-appropriate validations of analytical assays, ensuring regulatory alignment and accurate translation into IND and BLA sections.

Prior to Iovance, Rebecca worked at Beckman Coulter Life Sciences as a Senior Development Scientist for the development of flow cytometer clinical applications. Rebecca designed and executed studies for the development of clinical applications for IVD medical devices as per CLSI and FDA guidelines. Rebecca supported 510k submissions and subsequent information requests.

Rebecca received a B.S. in Animal Sciences from Iowa State University and a Ph.D. in Microbiology/Immunology from Virginia Tech.