Medical Device Quality Engineer — DV&V & Risk Mgmt
Listed on 2026-10-06
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Engineering
Quality Engineering, Biomedical Engineer, Medical Device Industry
Katalyst CRO is seeking a Quality Engineer with 4–6 years in medical device quality engineering to support DV&V, design controls, risk management, and regulatory compliance throughout product development.
Responsibilities include reviewing verification protocols, executing test method validations, and collaborating with cross-functional teams to drive quality improvements. Experience with FDA/ISO 13485 is preferred.
This role, Medical Device Quality Engineer — DV&V & Risk Mgmt at Katalyst CRO, could be your next career step.
We are looking to fill the Medical Device Quality Engineer — DV&V & Risk Mgmt position at Katalyst CRO in Santa Clarita, CA, United States.
The Medical Device Quality Engineer — DV&V & Risk Mgmt role at Katalyst CRO is now open for applications in Santa Clarita, CA, United States.
Join us at Katalyst CRO as our next Medical Device Quality Engineer — DV&V & Risk Mgmt in Santa Clarita, CA, United States.
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