Post-Market Safety & Risk Lead (Medical Devices)

Katalyst CRO seeks a PMS Specialist to manage post-market product safety surveillance and risk management initiatives. You will coordinate PMS plans, reports, and PSURs while driving CAPAs and ensuring regulatory alignment across FDA/EU-MDR environments. The role requires 4–5 years in post-market surveillance, strong regulatory knowledge, and cross-functional collaboration with Medical Affairs, R&D, Services, and Complaint Handling. Expect a compliance-focused, fast-paced work setting.