Regulatory Affairs Intern
Roche · Abidjan
Description du poste
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.
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Roche
Abidjan