Senior Quality Engineer - Medical Devices & Validation
Listed on 2026-10-06
-
Engineering
Quality Engineering, Biomedical Engineer -
Quality Assurance - QA/QC
Quality Engineering
Katalyst CRO is seeking a Quality Engineer with 5+ years in the medical device sector. You will drive quality processes, validation, and manufacturing support for surgical products and implants, ensuring compliance with GMP, ISO 13485, and FDA requirements.
Responsibilities include process validation, risk assessments, and data-driven decision making, with cross-functional collaboration across engineering and operations teams.
We are looking to fill the Senior Quality Engineer - Medical Devices & Validation position at Katalyst CRO in Louisville, KY, United States.
All applications are reviewed carefully by our team.
The position is based in Louisville, KY, United States.
This opportunity is part of our work in Engineering.
The advertised compensation is 85..
We aim to respond to suitable candidates as soon as possible.
Full responsibilities and requirements are described in the listing above.
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).