Description
We are looking for a
CMC Specialist (m/f)
Reference: -en
Start: 11/15
Duration: 3 MM++
Place: in Denmark
Branch: Pharmazeutische Industrie
Your tasks:
- Writing registration documents within API
- Method transfer
- Writing reports
- Method validation
- Stability studies
Your qualifications
- Analytical development background/regulatory affairs background (CMC)
- Fluency in English
- Knowledge of Danish
Skills:
- Regulatory affairs manager
Keywords: Regulatory Affairs Manager