Regulatory Affairs Specialist I IVD/CDx (Lab)
ARUP Laboratories
ARUP Laboratories is seeking a PharmaDx Regulatory Affairs Specialist I to support the development and submission of lab-developed tests and companion diagnostics to FDA and other global regulators. The role involves IRB/ethics approvals, PDP documentation, and risk management within the PharmaDx program.
You will collaborate with cross-functional teams, prepare regulatory submission packages, and assist during audits.
#J-18808-LjbffrVacancy posted 1 day ago
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