We are looking for a qualified Validation Engineer to join top-talented multidisciplinary Engineering team and. The Validation Engineer will be responsible for validating all of the production tools and equipment ,documenting them, and serving as the professional Focal Point for validation.
Key Responsibilities:
- Writing machine documents, such as URS, FDS, FMEA, and user manuals
- Writing validation documents, such as IQOQPQ PV and others
- Performing validations
- Project management on production lines
Position Requirements:
Requirements:
- Experience of 3 years or more in writing validation in the production lines of Medical Device / Pharma companies.
- Bachelor%27s degree in mechanical engineering/biomedical or another scientific degree.
- Ability to manage projects
- Good Technical understanding
- Computer Skills – office%28a must%29
- ms-projects, writing documents %28an advantage%29
%2A%2A The job includes traveling to our factory in Tiberias %2A%2A
