Hybrid GRA Device Associate – IVD & Medical Devices

A global biopharma company is searching for a GRA Device Associate to contribute to regulatory strategies for in-vitro diagnostic technologies. This role requires collaboration with cross-functional teams and regulatory authorities to facilitate product approvals. Candidates should have at least 6 years of experience in the pharmaceutical or medical device industry, with a focus on IVD regulatory processes. The position involves preparing regulatory submissions, risk assessments, and managing compliance while working in a hybrid environment (60% on-site). Competitive compensation and benefits package included. #J-18808-Ljbffr