Regulatory Affairs Program Manager

  • Posted: 31/03/2023
  • Salary: Competitve
  • Location: Zug, Switzerland
  • Job Type: Permanent/Fixed Term

Our client, A Global Biotech Company, are currently looking for a Regulatory Affairs Program Manager to join their team, focused on their innovative vaccine projects. A minimum of 3 Years in Regulatory Program/Documentation experience is require for this position.


  • Responsible for developing plans for major submission projects.
  • Deliver on high-level project management charts, estimations for budgets, timeline management, MAAs/BLAs and major variations.
  • Work specifically VEEVA RIM management systems.
  • Work closely on post-authorization projects and regulatory development.

Experience Required

  • 3-5 Years' Experience in Pharma/Biotech Industry.
  • 3-5 Years' Experience in Regulatory Affairs/ Regulatory Program Systems/ Document Management Systems (VEEVA RIM)
  • Degree in Life Science Related Field.
Owen Nash Associate Consultant

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