Job responsibilities
-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
Minimum qualifications1
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Bachelor’s Degree in Pharmacy
3 Years of relevant experience
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2
Master’s Degree in Pharmacy
1 Years of relevant experience
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3
Bachelor’s Degree in Biotechnology
3 Years of relevant experience
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4
Master’s Degree in Biotechnology
1 Years of relevant experience
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5
Bachelor’s Degree in Pharmaceutical Sciences
3 Years of relevant experience
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6
Bachelor’s Degree in Molecular Biology
3 Years of relevant experience
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7
Master’s Degree in Molecular Biology
1 Years of relevant experience
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8
Master’s Degree in Pharmaceutical Sciences
1 Years of relevant experience
Required competencies and key technical skills
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1Investigation skills
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2Resource management skills
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3Problem solving skills
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4Decision making skills
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5Time management skills
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6Risk management skills
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7Results oriented
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8Digital literacy skills
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9Fluency in Kinyarwanda, English and/or French. Knowledge of all is an added advantage
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