Description
We are looking for a
Specialist Regulatory Affairs (m/f)
Reference: -en
Start: asap
Duration: 12 MM++
Place: in the Basel region
Branch: Herstellung von pharmazeutischen Erzeugnissen
Your tasks:
- Support a senior DRA project leader in the field of post approval and other development activities
- Create and finalize regulatory documents, handle variations and assist in international filings
- Coordinate with affiliates and support as well as represent DRA in cross-departmental meetings
Your qualifications
- University degree in Life Sciences, Pharmacy or Medicine
- Profound experience in the field of European DRA
- Good knowledge of the European regulatory framework including documentation and procedures
- Outstanding cross-cultural communication skills in English, in both verbal and written form (German and/or French is of advantage)
Skills:
- Regulatory affairs manager
- Regulatory affairs assistant
Keywords: Regulatory Affairs Manager