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To conduct dossier assessment for product registration To participate in the develop and review of necessary regulatory tools such as regulations, guidelines, SOPs, and official forms within the regulatory framework to standardize and improve the assessment procedures, To contribute establishment, review and updating of the register of radiopharmaceuticals and radiotherapy products with variations, new registrations and deletions due safety and quality issues, To sample radiopharmaceuticals and radiotherapy products from the market and liaise with the Division of Quality Control Laboratory for analysis, To participate and conduct operational research, programmes and projects within the Division. To demonstrate the ability to consistently provide quality services that meet customer and regulatory requirements within his/her division to meet Rwanda FDA quality objectives. To participate in organized training in Quality Management System. To do the assigned tasks (job) by fully implementing the QMS established requirements.