Regulatory Affairs Intern

About the role

Join Roche’s Medical Affairs & License to Operate chapter as a Regulatory Affairs Intern. You will support the preparation and coordination of regulatory submission packages, ensuring compliance with local and regional requirements and Roche’s internal policies.

Key responsibilities

• Analyze and communicate internal and external regulatory intelligence.
• Adapt global product dossiers to local requirements and manage regulatory registration filings across product life cycles.
• Monitor and communicate filing status, ensuring readiness for inspections.
• Review promotional and non‑promotional material for regulatory compliance.

Required profile

• Recent graduate (max 2 years experience) with a University degree in Pharmacy, Medicine, or a related pharmaceutical/biological discipline (Pharm D preferred).
• Fluent in French with basic written and spoken English and a commitment to improve language skills.
• Self‑managed, eager to learn, able to prioritize and work effectively with cross‑functional teams.

Required skills

• Ability to use digital tools and systems for regulatory activities.
• Strong listening, questioning, and clear communication abilities.