Regulatory Affairs Manager, Africa
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In this role you will lead regulatory programs across Africa, shaping patient access and lifecycle management for diverse markets. You will coordinate registrations and collaborate with local partners and authorities to deliver compliant outcomes. You’ll work with cross-functional teams and clients to drive timely regulatory decisions and deliver project excellence. This is a strategic role with global capabilities, offering broad exposure to Francophone and Anglophone markets and impactful product registrations.
Compensaciones / Beneficios
• Lead regulatory projects across multiple African markets
• Manage submission preparation, quality review, compilation and tracking activities
• Coordinate product registrations, renewals, variations and lifecycle management programs
• Collaborate with local applicants, regulatory partners and health authorities
• Monitor project timelines, deliverables and risks
• Provide regulatory guidance to internal and external stakeholders
• Lead client governance meetings and provide regular project updates
• Maintain regulatory documentation and ensure country-specific compliance
• Contribute to delivery excellence and continuous improvement initiatives
Responsabilidades
• Bachelor's degree in Pharmacy, Life Sciences, Medicine or related discipline
• Minimum 5 years of Regulatory Affairs experience
• Experience xghoner supporting multiple African markets
• Strong knowledge of regulatory requirements across French-speaking and English-speaking African countries
• Experience with registrations, renewals, variations and lifecycle management activities
• Strong client-facing, communication and project management skills
• Experience managing external regulatory vendors or local partners
• Fluent French and English, written and spoken
Requisitos principales
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