Currently we are looking for a Regulatory Affairs CMC consultant for a global pharmaceutical company in Switzerland. The contract would be for the duration of 4 months.
The consultant will be responsible for leading CMC regulatory submissions and will serve as an internal contact for CMC activities.
- Minimum 5 years of experience in CMC activities including submissions to regulatory agencies
- Good knowledge of development of drug substance and drug product
- FDA, ICH and EMA regulations knowledge for CMC/Quality