Regulatory Affairs Intern
Roche · Abidjan
Description du poste
About the role
We are seeking a motivated intern to join Roche’s Medical Affairs & License to Operate chapter within the Regulatory Affairs department. The intern will support the preparation and coordination of regulatory submission packages, ensuring compliance with local and regional requirements and company policies.
Key responsibilities
- Analyze and communicate internal and external regulatory intelligence.
- Provide regulatory input during cross‑functional Affiliate business meetings.
- Adapt global product dossiers to local requirements and manage regulatory registration filings throughout product life cycles.
- Monitor and communicate filing status and perform affiliate regulatory activities on Roche systems.
- Support inspection readiness and ensure compliance for marketed products.
- Review promotional and non‑promotional material for regulatory compliance.
Required profile
- Recent graduate (≤2 years experience) with a university degree in Pharmacy, Medicine or a related pharmaceutical/biological discipline (Pharm D preferred).
Required skills
- Fluency in French.
- Basic written and spoken English with a commitment to improve.
- Ability to work autonomously, prioritize tasks and collaborate with cross‑functional teams.
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Roche
Abidjan
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