Teams at ARUP Laboratories

Support regulatory development and submissions for lab-developed tests and companion diagnostics (IVD), including IRB/ethics, IDE/PMA and other filings; implement Design Control and risk management; prepare regulatory communications; support audits, supplier questionnaires, and continuous improvement within PharmaDx Quality and Regulatory Affairs.

Lead enterprise vulnerability management: research and validate vulnerabilities, prioritize remediation, perform risk assessments, exploit development and pen-testing, support SOC incident response, produce reports and training, and collaborate with IT/Dev teams to reduce cyber risk.