Beschreibung
For our customer in Solothurn we are looking for Subject Matter Experts Junior/Normal
Your responsibilities:
Acting as a reviewer of changes conducted for marketed medical devices in order to:
- assess and document completeness of change assessment with focus on Regulatory aspects
- identify and document deficiencies
Required Skills:
- Basic understanding of European Medical Device Regulations
- European Medical device industry experience especially with regulatory, labeling, quality or engineering
- Experience in technical and or scientific writing
- Familiarity with clinical and non-clinical data literature searches (eg PubMed)
- German and English (oral and written is an absolutely must)
If you are interested in this position please do not hesitate to send us your CV electronically.