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Katalyst CRO seeks a Post Market Surveillance Specialist to lead safety surveillance and risk management across Medical Affairs, Clinical, R&D, Services and Complaint Handling. You will ensure PMS and RM processes are executed end-to-end, review aggregate data, and escalate as needed. Responsibilities include creating PMS plans/reports, PSUR preparation, CAPA ownership, and cross-functional collaboration to meet FDA/EU MDR requirements.

Also on the board Same function, level within a rung

Level

Senior

Location

Somerville, MA

Occupation

Regulatory Affairs Managers

Industry

Electromedical and Electrotherapeutic Apparatus Manufacturing

Posted

yesterday

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