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Group Head Of Regulatory Affairs ƒƒ‚ƒ‚‚ƒ‚‚“ Healthcare Sector (Nairobi) At Talent Grid Africa

Talent Grid Africa

Consulting full time Nairobi Posted 1 day ago

Talent Grid Africa is a regional consulting firm that partners with leaders in business to handle the complexities of hiring the right talent, engaging them in the right way, improving performance, and retaining top talent. We help them leverage their greatest assets-the people, to capture more opportunities and grow their businesses. Our purpose is to offer human resource and business solutions that are innovative, actionable, and compliant, that solve organizations’ most important challenges. Our success depends on the true belief that people are the drivers of any business, and an optimized workforce equals business success. We work with a diverse team of experts in strategic HR management and acquisition that delivers local solutions for global business success.This role is critical in shaping regulatory strategy, ensuring compliance, and enabling successful market expansion for both human pharmaceutical and animal health products. The successful candidate will lead: Regulatory strategy development and execution ACTD/CTD dossier preparation and submissions Product registrations, renewals, and lifecycle management Regulatory engagement across multiple African countries Coordination with CMOs, CROs, QA, R&D, and Supply Chain teams Implementation of RIMS and digital regulatory systems Team leadership, capability building, and performance management Key Requirements To be considered for this role, candidates should have: Bachelor’s degree in Pharmacy, Veterinary Medicine, Pharmaceutical Sciences, or a related scientific field Minimum 7+ years of regulatory affairs experience within the pharmaceutical industry, with exposure to African markets Strong experience in ACTD/CTD dossier preparation, submission, and review Proven experience in product registrations, renewals, variations, and lifecycle management Experience working with both locally manufactured products and CMOs (preferred) Experience coordinating bioequivalence studies with CROs (preferred) Strong understanding of pharmaceutical regulatory frameworks across multiple African countries Experience with regulatory systems, tracking tools, or RIMS platforms is an added advantage Strong leadership, stakeholder management, and cross-functional collaboration skills