We are seeking a dynamic Regulatory Affairs Lead to drive regulatory strategy and compliance across the region. The ideal candidate will lead product registrations, manage regulatory submissions, engage with health authorities, and support business growth through effective regulatory planning and execution. Strong communication, stakeholder management, and strategic thinking skills are essential.
Responsibilities
Oversight of Pharmacovigilance functions as LPVRP for Kenya, Tanzania, Uganda, Zimbabwe, Zambia, Ethiopia, Rwanda, Burundi, Nigeria, Malawi, Ghana, Mozambique
Appointed and notified QPPV to Kenya PPB, Rwanda FDA and Zimbabwe MCAZ as required
Responsible for the registration and life cycle management of products in Kenya
Oversight role on the registration and life cycle management of products in Tanzania, Uganda, Zambia, Rwanda, Zimbabwe, Burundi
Responsible for overseeing and managing transactions in registering new and existing products and maintaining...