Senior Medical Device Process Validation Engineer
Listed on 2026-10-13
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Engineering
Biomedical Engineer, Medical Device Industry, Validation Engineer, Quality Engineering
Katalyst CRO is seeking an experienced Process Validation Engineer to support process validation, equipment qualification, and manufacturing quality activities within a medical device environment in Nebraska. You will ensure FDA and ISO 13485 compliance while supporting transfers and process improvements.
Responsibilities include developing IQ/OQ/PQ protocols, maintaining validation documentation, and utilizing PLM Agile for change orders.
The Senior Medical Device Process Validation Engineer role at Katalyst CRO is now open for applications in Norfolk, NE, United States.
The following position is for a Senior Medical Device Process Validation Engineer with Katalyst CRO.
Our group is growing, and we are hiring a Senior Medical Device Process Validation Engineer in Norfolk, NE, United States.
This position is for the Senior Medical Device Process Validation Engineer role at Katalyst CRO.
We are seeking a motivated Senior Medical Device Process Validation Engineer to join Katalyst CRO in Norfolk, NE, United States.
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