Academic Positions - Health Device Innovation

Durban University of Technology · Durban, KwaZulu-Natal

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Position 1

  • Professor: Biosensors, Microfluidics, In-Vitro Diagnostics and Clinical Validation
  • Theme 1: Point-of-Care Diagnostics and Essential Clinical Devices
  • Reference Number: 30002774
  • Status of Position: Permanent
  • Reporting Line: Director: DUT Health Devices Innovation Institute
  • Theme-specific expertise
  • Biosensors, microfluidics, in-vitro diagnostics and clinical validation

Minimum requirements

  • A relevant doctoral degree NQF Level 10 in Biomedical Engineering, Medical Physics, Electrical Engineering, Clinical Laboratory Science, Biomedical Science or a closely related qualification to the theme.
  • A strong record of research and/or academic leadership, with demonstrated leadership in the relevant scholarly field.
  • A substantial and sustained period of distinguished academic experience in research and/or professional experience in higher education or a research environment, with recognised standing in the field.
  • A minimum of ten DHET-accredited research outputs or recognised creative/innovation outputs during the preceding three years, relevant to the field.
  • Evidence of substantial record of successful supervision to completion of Master's and Doctoral students.
  • A sustained record of high-quality, cited research; competitive grant awards; international recognition; and leadership of substantial interdisciplinary programmes.
  • Evidence of excellent teaching, postgraduate mentorship, curriculum contribution and academic citizenship appropriate to appointment at Full Professor level .
  • Demonstrated success in securing competitive research funding grants, contracts or commissioned research.
  • Evidence of leading multidisciplinary teams and building national/international research collaborations.

Key responsibilities

Research Leadership

  • Lead an internationally credible portfolio of affordable point-of-care and near-patient diagnostic technologies for priority infectious, maternal-child and non-communicable conditions.
  • Develop, lead and grow a high-quality, externally funded research programme encompassing biosensors, microfluidics, imaging systems and essential clinical monitoring devices.
  • Develop research on analytical performance, clinical validity, real-world performance, calibration, consumables, shelf life and sample pathways.
  • Establish co-led clinical-validation programmes with authorised health-service partners and appropriate biostatistical support.
  • Lead analytical performance verification, clinical validation, usability and real-world evidence generation for device prototypes.
  • Generate peer-reviewed outputs, protectable intellectual property where appropriate, translational evidence and standards or policy contributions.
  • Ensure all research proceeds through proportionate ethics, risk, regulatory and clinical evidence pathways in accordance with SAHPRA and applicable standards.
  • Postgraduate Supervision and Teaching
  • Build competitive multi-partner grants, laboratories/platforms and postgraduate cohorts linking engineering, clinical science, data and implementation.
  • Supervise doctoral and master's students across Theme 1 research streams, with a commitment to timely completions.
  • Mentor junior researchers, postdoctoral fellows and research associates within the Institute.

Partnership and Funding

  • Establish and maintain formal clinical, community and industry partnerships for needs identification, co-design and clinical evaluation.
  • Lead or co-lead grant applications, contracted research and philanthropic funding proposals to sustain and grow the research programme.
  • Represent the Institute in relevant national and international professional forums, standards bodies and policy engagements.

Governance and Compliance

  • Implement the Institute's stage-gate governance framework for all Theme 1 projects, including ethics approvals, design controls, risk registers and documentation standards.
  • Report on Theme 1 performance against agreed targets to the Institute Director and relevant governance structures.
  • Maintain audit readiness and contribute to quality assurance across the Institute's research portfolio.

Ideal / additional recommendations

  • An NRF rating or demonstrated equivalent international standing through publications, citations and scholarly recognition is strongly advantageous.

Position 2

  • Senior Lecturer: Essential Monitoring, Maternal-Neonatal Devices and Human Factors
  • Theme 1: Point-of-Care Diagnostics and Essential Clinical Devices
  • Reference Number: 30002778
  • Status of Position: Permanent
  • Reporting Line: Director: DUT Health Devices Innovation Institute
  • Theme-specific expertise
  • Essential monitoring, maternal-neonatal devices and human factors

Minimum requirements

  • A relevant doctoral degree NQF Level 10 in Biomedical Engineering, Medical Physics, Electrical Engineering, Clinical Laboratory Science or a closely related field.
  • A developing record of research and/or academic leadership in the relevant scholarly field.
  • An appropriate period of relevant academic experience in research and/or professional experience in higher education or a research environment.
  • At least three DHET-accredited research outputs or recognised creative/innovation outputs during the preceding three years.
  • Evidence of participation in supervision of Master's students.
  • Evidence of excellent teaching, innovative assessment or curriculum practice, effective academic advising and a developing independent research programme.
  • Evidence of participation in grants writing.
  • Evidence of participation in multidisciplinary teams and research collaborations.
  • Evidence of participation in grants writing.
  • Evidence of participation in multidisciplinary teams and research collaborations.

Key responsibilities

Research

  • Design and evaluate essential monitoring, triage, medication-support or maternal-neonatal devices for constrained care environments.
  • Conduct human-factors, usability, workflow, language, training and referral-integration studies with users and clinicians.
  • Develop traceable device requirements, verification protocols and research documentation from concept stage.
  • Contribute to Theme 1 research in essential monitoring devices or related streams under the leadership of the Theme 1 Professor.
  • Participate in the KZN Frontline Diagnostics and Essential Devices Platform, contributing to analytical verification, usability evaluation and clinical evidence generation.
  • Maintain compliance with Institute ethics, risk and design-control requirements in all research activities.
  • Pursue external research funding through grants, fellowships and contracted research.
  • Postgraduate Supervision and Teaching
  • Co-supervise and progressively lead master's-level research projects within Theme 1.
  • Publish research, supervise postgraduate candidates and contribute to interdisciplinary teaching and methods development.
  • Contribute to undergraduate and postgraduate teaching in biomedical engineering, diagnostic science or related disciplines in collaboration with DUT faculties.
  • Support and mentor postgraduate students and junior researchers within the Institute.

Partnership and Engagement

  • Support prototype testing, field studies, grant proposals and innovation or knowledge-transfer activities.
  • Participate in clinical and community needs-identification activities and formal co-design workshops with health-service and industry partners.
  • Contribute to grant applications, technical reports and deliverables for funded projects within Theme 1.
  • Engage with professional bodies and participate in relevant seminars, workshops and community engagement activities.

Administration and Governance

  • Contribute to Institute governance activities, including stage-gate documentation, ethics submissions and project reporting.
  • Participate in performance review processes and Institute quality-assurance activities as required.

Ideal / additional recommendations

  • Experience in biomedical
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