UCT is one of the leading higher education institutions on the African continent and has a tradition of academic excellence that is respected worldwide.
Situated on spectacular Devil’s Peak, it is Africa’s oldest and foremost university. Three worldwide rankings have placed UCT among the world’s top 200 institutions, the only African university to have...
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Undergraduate and postgraduate qualifications in Biomedical Engineering or a related engineering discipline.
PhD in Biomedical Engineering or a closely related field.
A minimum of 5 years of post-doctoral experience in biomedical engineering with a focus on medical devices, or equivalent experience at lecturer level in biomedical engineering with research on medical devices, or comparable experience in the medical device industry.
Evidence of a research track record in the fields of medical device design, medical device innovation and translation.
Successful supervision /co-supervision of postgraduate students (to completion/ ongoing) at master’s and/or PhD level or a similar level medical device project management experience
A research track record that demonstrates peer recognition, experience (e.g. postdoctoral, industry), productivity and creativity, such as peer-reviewed journals / patents / registered designs or recognised product industrialisation.
A minimum of 2 years of work experience in medical device regulatory systems and quality management systems including ISO 13485 and SAHPRA).
Advantages:
Work experience in medical device regulatory systems and quality management systems including CE Marking, FDA and other regulatory bodies
Success in the solicitation of funding for research and / or fund raising for medical device product Industrialisation
Responsibilities:
Contribute strongly to teaching undergraduate and postgraduate courses in biomedical engineering, including medical device design. This may include modules on medical device innovation and the regulatory and quality frameworks governing medical devices (ISO 13485, CE marking, FDA).
Develop and support research relating to medical device design and innovation, including industry partnerships, regulatory compliance (ISO 13485, CE marking, FDA), and translation of medical devices into manufacturing and clinical use, with appropriate training and supervision of postgraduate students.
Foster and grow industry partnerships in support of medical device research, development, manufacturing, and commercialisation.
Contribute to the department's well-being and smooth operation.
Contribute to administration at a rank-appropriate level.
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