Execute surface plasmon resonance (SPR) analysis for small molecules binding to protein and/or protein interactions. Work both independently and as part of a team to ensure project team goals and deliverables are met. Communicate effectively and present results in cross functional team meetings Trouble shoot and solve scientific problems with minimal supervision. Be highl

Serves as the Regulatory Affairs lead on cross functional MDR project teams Ensures compliance with EU Medical Device Regulations (MDR) and EU guidance throughout the project. Actively participates in EU MDR project teams by attending meetings, collaborating with the project manager and cross functional team members, and communicating regulatory requirements and guidance