One of our largest medical device clients in the Midwest is currently looking for a Senior Quality/Validation Engineer:
- Responsible for writing/contributing to, and reviewing Process risk assessment documents &Process validation documents
- Responsible for writing and executing Test Methods and Test Method Validations, as well as Manufacturing Control Plans.
- Must have Medical Device experience and process knowledge (machining, polishing, blasting, packaging)
- Engineering degree required, Excellent technical writing skills / GDP knowledge
- Must have process risk assessment experience
- 5+ years of quality experience preferred
- Previous medical device experience preferred
Sthree US is acting as an Employment Business in relation to this vacancy.
Data source
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