We have a wonderful opening for a Quality Engineer to join an international medical device company. The role is based in the beautiful town of Oberdorf in Basel, and is a contract position until the end of this year. The ability to speak fluent German is requirement for this role.
- The key purpose of this role is to support process validation strategy, write and implement engineering studies and process validation protocol including summary reports.
- You will aid manufacturing operations in all areas to prepare for the MDR changes coming in 2020.
- In addition you conduct investigation, bounding, documentation, review and approval of non-conformances, customer complaints and CAPAs.
Find out more and apply here
