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Regulatory Affairs Program Manager
- Posted: 30/03/2023
- 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.
Responsibilities
- 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