Global Regulatory Device Associate (IVD/Diagnostics)

A leading biopharmaceutical company is looking for a GRA Device Associate to shape global regulatory strategies for in-vitro diagnostic technologies. This role requires collaboration across teams, regulatory guidance, and the opportunity to directly influence product approvals. Candidates should have over 6 years of experience in the pharmaceutical or biotechnology industry, with specific focus on IVD regulations. The position is located in the United States, offering both on-site and hybrid work options, providing a rewarding career journey with excellent benefits. #J-18808-Ljbffr