Regulatory Affairs Project Manager

At Roche, you can show up as yourself and thrive both personally and professionally. As an International Regulatory Project Manager, you will support and deliver high-quality regulatory submissions of IVDs (including companion diagnostics) to Health Authorities worldwide.

Requirements

• Bachelor’s / Master degree in Life Science, Data Science or related subject or equivalent experience
• At least 5 years experience in Regulatory, R&D, Quality, Operations and/or Clinical
• Experience in diagnostics (highly preferred) or pharmaceutical regulatory affairs