Regulatory Intelligence Associate

About the role

The Regulatory Intelligence Associate will support the company by monitoring, analysing and communicating regulatory developments across the Middle‑Africa region. This role ensures that the organisation stays compliant and can quickly adapt its products and processes to new requirements.

Key responsibilities

• Collect regulatory intelligence from competent authorities, government bodies, regulatory agencies and official publications across 47 Middle‑Africa countries, covering acts, guidelines, forms, circulars, policy updates and more.
• Assess the relevance, impact, urgency and compliance obligations of the gathered intelligence for the company’s product portfolio, perform gap analyses and prioritize actions based on business risk and deadlines.
• Prepare and distribute structured intelligence reports, alerts and impact‑assessment documents to cross‑functional teams such as Regulatory Affairs, Pharmacovigilance, Marketing, Medical Affairs, Supply Chain, and Quality Assurance, and present findings in governance meetings.

Required profile

• Mid‑level professional with at least 36 months of experience in regulatory intelligence, regulatory affairs or related functions within the healthcare or pharmaceutical sector.
• Familiarity with regulatory frameworks and documentation in the Middle‑Africa region.
• Strong analytical and communication abilities to evaluate and convey regulatory changes to diverse stakeholders.

Required skills