Job responsibilities
To screen, assess and prepare feedback to the applications for registration of Controlled Substances. To submit samples for testing and ensure that the results are available for use in assessment process. To efficiently use resources and ensure the compliance of product registration, review guidelines and to streamline the processes. To improve Controlled Substances assessment standard by adopting and harmonizing international standards and best practices. To assess product variation applications and propose approvals on changes made to registered products to the Division Manager. 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.
Minimum qualifications
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1Bachelor’s Degree in Pharmacy
3 Years of relevant experience
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2Master’s Degree in Pharmacy
1 Years of relevant experience
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3Bachelor’s Degree in Chemistry
3 Years of relevant experience
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4Bachelor’s Degree in Biotechnology
3 Years of relevant experience
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5Master’s Degree in Chemistry
1 Years of relevant experience
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6Master’s Degree in Biotechnology
1 Years of relevant experience
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7Bachelor’s Degree in Pharmaceutical Sciences
3 Years of relevant experience
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8Master’s Degree in Medicine
1 Years of relevant experience
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9Master’s Degree in Pharmaceutical Sciences
1 Years of relevant experience
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10Bachelor’s Degree in Human Medicine
3 Years of relevant experience
Required competencies and key technical skills
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1Resource management skills
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2Problem solving skills
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3Decision making skills
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4Time management skills
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5Risk management skills
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6Results oriented
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7Digital literacy skills
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8Fluency in Kinyarwanda, English and/or French. Knowledge of all is an added advantage.
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