GA
Regulatory Affairs and Licensing- Francophone Africa Lead
NOUVEAUCDIabout 2 hours ago
Job Description
Sénégal
CDI
⚠️
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Description non disponible. Consultez l'offre sur le site d'origine pour plus de détails.
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What this role involves
You will lead regulatory submissions and licensing strategies for Francophone African markets, coordinating with local health authorities and internal teams to secure product approvals. Day-to-day tasks include monitoring regulatory changes, preparing dossiers, and managing timelines for market access across Senegal and neighboring countries.
Key skills to highlight
Proven expertise in pharmaceutical regulatory affairs, especially with ARIPO or OAPI frameworks. Fluency in French and English is essential, along with experience in dossier compilation (e.g., CTD format) and direct liaison with national medicines agencies. Strong project management and cross-cultural negotiation skills will set you apart.
Taf4All CV tip
List specific regulatory approvals you’ve secured in Francophone Africa (e.g., Senegal, Côte d’Ivoire, Cameroon) with dates and product types. Use a table in your CV to show submission-to-approval timelines, emphasizing speed and compliance. Avoid generic phrases like "regulatory experience"—be precise.
Before you apply
Verify this role on Gamjobs’ official site or LinkedIn to ensure it’s not a scam. Legitimate recruiters won’t ask for upfront fees or sensitive personal data. Cross-check the company’s registration in Senegal and look for direct contact details.
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Beware of scams
Taf4All only lists job offers published by third parties — we are not the source of these jobs and do not handle recruitment. Stay vigilant: never pay money to get a job or an interview, and be wary of any suspicious request.