Technical Regulatory Affairs Manager – Basel

We have an excellent opportunity for a Technical Regulatory Affairs Manager to join a company in the drug discovery industry in Basel. This position is offered on a contract basis between 6 to 12 months. The ideal candidate will execute with following tasks:

  • Write and update the Module 2 (Quality Overall Summary) and the Module 3 (drug substance and drug product quality sections) of the CTD/NDA Applications
  • Create Briefing Books and supportive documentation for Health Authority meetings (pre-IND, pre-NDA, End of Phase II, Scientific Advice meetings)
  • Support and advise the project team regarding pharmaceutical development related to regulatory strategy for submission

If you are interested in this role contact our Swiss Team here or apply here

Find out more here

Posted in: Job of the Week, News
Two women working at a pharmaceutical company