Regulatory Affairs Scientist (Fixed-term contract
On behalf of an International Company based in Geneva, we are currently looking for a: Purpose of the role: Under the responsibility of the Global Head Regulatory Affairs Infectious Disease /OTX, you will be part of the Technical Regulatory Affairs and will support timely preparation of high quality drug substance and/or drug product Quality (CMC) documentation, to support global regulatory submissions. Your responsibilities: Contribute to the definition of the CMC regulatory strategy for new registration and life cycle activities Write an update high-quality CMC documentation, Read more […]