Full Time Senior Urgent Deadline: 2026-04-15

Zenufa Laboratories is looking for a dynamic Regulatory Affairs Manager to lead our regulatory strategy across Tanzania and the East African Community (EAC) region.

This is a key leadership role responsible for ensuring all our products meet regulatory requirements and maintaining our strong market position.

• BPharm degree (Master's in Regulatory Science or related field preferred)
• Pharmacy Council registration
• 7+ years experience in pharmaceutical regulatory affairs
• Deep knowledge of TMDA, EAC, and WHO prequalification processes
• Experience with CTD/eCTD dossier preparation
• Strong project management and leadership skills

• Lead regulatory submissions to TMDA, EAC, and other regional authorities
• Develop and implement regulatory strategy for new product launches
• Manage product registration dossiers and renewals
• Ensure compliance with GMP, GDP, and local pharmaceutical regulations
• Liaise with TMDA and international regulatory bodies
• Lead a team of 4 regulatory affairs specialists
• Monitor regulatory changes and advise management on implications

• Competitive salary package
• Performance bonus
• Company vehicle
• Health insurance (family)
• Professional development budget
• International travel opportunities

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About the Company

Zenufa Laboratories is a leading Tanzanian pharmaceutical manufacturer producing over 200 products including tablets, capsules, syrups, and injectable preparations for the local and regional market.