Global IVD Regulatory Device Associate

A leading biotechnology company in the United States is seeking a GRA Device Associate to contribute to global regulatory strategies for in-vitro diagnostic technologies. This role involves collaborating with cross-functional teams, optimizing product development, and influencing product approvals through strategic interactions with health authorities. The ideal candidate will have over 6 years of experience in the pharmaceutical or medical device industry, with strong skills in regulatory documentation and a Bachelor's degree in a scientific field. #J-18808-Ljbffr