Global Regulatory Device Associate – IVD & Diagnostics

A global biopharma company is seeking a GRA Device Associate to support regulatory strategies for in-vitro diagnostics. This role involves collaborating with cross-functional teams, navigating regulatory landscapes, and influencing product approvals. Ideal candidates will have over 6 years in the pharmaceutical industry, with substantial experience in IVD regulation. A strong background in regulatory documentation and communication is essential. Opportunities for growth and career development are offered, along with a hybrid working model. #J-18808-Ljbffr