The Ugandan Jobline

• Regulate, control, and monitor all matters related to medical devices and surgical instruments, stakeholders and Conformity Assessment Bodies.
• Actively coordinate and supervise establishment of the standards for compliance with conformity assessment procedures of medical devices (evaluate new techniques / reagents)
• Manage and monitor post-market surveillance and vigilance system of medical devices used in the country.
• Ensure and supervise the timely regular inspection and certification of premises dealing in the manufacture, importation, storage , distribution, dispensing of medical devices (including those for human and veterinary use) in both the private and public sectors.
• Coordinate and conduct assessment of medical device manufacturers for Good Manufacturing Practice (GMP) compliance prior recommendation for product market authorization.
• Coordinate and participate in the verification of pro-forma invoices for importation of medical devices and equipment; and ensure compliance with registration and other requirements.
• Actively collaborate with Uganda Revenue Authority, Police and other security organs to investigate suspected cases of illegal/criminal activities related to medical device importation,(chemicals / reagents) handling, distribution and use.
• Responsible for the sensitization of various stakeholders on the need to comply with the provisions of the National Drug Policy and Authority Act Cap 206 of the Laws of Uganda (revised edition 2000).
• Compile and prepare in collaboration with the head of department quarterly and annual activity reports for the various units.
• Train and mentor new employees, prepare work schedules, monitor and evaluate performance.
• Perform any other duties assigned by the supervisor from time to time

• The applicant must hold a Master’s Degree in Biomedical Sciences
• Possession of a Bachelor’s Degree in Biomedical Sciences from a recognized Institution.
• Registration with the relevant professional body.
• At least eight (8) years’ experience in a reputable organization or company, with at least three years in a senior position.
• Past exposure and experience with GMP inspection is an added advantage
• Good working knowledge of various aspects of medical device regulation.
• Training in management
• Computer literacy i.e. Proficiency in computer applications especially Microsoft office packages
• Must be of high integrity
• Training and experience in Quality Management System Lead auditor ISO 9001 and ISO 17020 is an added advantage

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