Vaccines and Biosimilar Registration Specialist at Rwanda Food And Drugs Authority (FDA): (Deadline 2 May 2024)

-To participate in the preparation and implementation of business plan and budget for the Division, -To participate in the development and review of regulations, guidelines, manuals and SOP related to assessment and registration of human vaccines, biologicals and biosimilar and others similar documents that may be needed the Division or Department. – To contribute to the development, review and updating of the register of human vaccines, biologicals and biosimilar with variations, new registrations and deletions due safety issues, -To assess human vaccines, biologicals and biosimilar with variations, new registrations, and deletions due safety issues, -To Evaluate the quality, safety and efficacy of human vaccines, biologicals and biosimilar, -To Sample of human vaccines, biologicals and biosimilar from the market and liaise with the Division of Quality Control Laboratory for analysis, -To participate in Conduct of operational research, programmes and projects within the Division