Summary
Date Posted: Monday, July 29 2024, Base Salary: Not Disclosed

JOB DETAILS:
To Participate in the planning and budgeting of Post marketing surveillance activities within the country;
To develop and implement annual post marketing surveillance plan for human medical products;
To receive and record suspected substandard and or falsified medical (SF) products;
To develop and implement annual sampling plan for human medical products.
To conduct the investigation of the reported substandard and or falsified human medical products;
To recommend the regulatory actions based on post marketing surveillance data;
To conceive the call for quarantine and recall of medical products;
To disseminate the communications on detected substandard and falsified products on the market;
To conduct the recall audit of medical products;
To conduct general and targeted market surveillance (conduct product quality monitoring);
To collaborate with stakeholders to monitor the quality of medical products on the market;
To undertake random sample analysis of human medical products;
To Participate in the development and review of post marketing surveillance regulations, guidelines, training manuals, SOPs, and performance standards;
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.

Work Hours: 8

Experience in Months: 36

Level of Education: Bachelor Degree

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