Smith & Nephew
Project Manager, Evidence Evaluation
My background is in biomedical engineering, specifically biomaterials and biomechanics. I did medical device R&D for 2 years as an undergrad at the University of Pennsylvania, 5 years for my PhD at Rutgers University, 2 years for my post-doc at NIST, and 8 years in industry. I transitioned to regulatory affairs 4 years ago. I am now a project manager within Clinical, Scientific, and Medical Affairs (CSMA) at Smith & Nephew, getting CSMA ready for the new European Medical Device Regulations.