As Director, I am responsible for leadership and strategic direction of MDMC across the 5 university partners, and provide particular expertise on laser-based manufacturing processes.

As PI and manager of the MDMC, I supervise the HWU Technology Specialists and am responsible for the day-to-day running of the Centre. I also look at the sustainability of the MDMC from 2026 onwards. I specialise in systems integration and novel manufacturing processes.

As a Business Development Executive, I develop relationships between the MDMC and medical device manufacturing Companies. I provide initial support for prospective clients and identify new opportunities for the MDMC to enhance relationships with industry.

As a Technology Specialist, I take on technical responsibility for the success of client applications. I am the technical expert on laser-based manufacturing, liaising between SMEs and MDMC and providing solutions to ongoing and strategic enquiries.

As a Technology Specialist, I partake in client interactions by providing technical expertise on prototyping, additive and subtractive manufacturing, imaging, and analysis, promoting solutions that successfully meet client needs.

I am a technology specialist experienced in medical device research and development. Using the facilities at the MDMC, my role is to provide SMEs expertise and support as they develop and manufacture their medical devices.

I am a Technology Specialist, providing SMEs with expertise in the development of their medical devices and products. My primary goal is to find solutions which successfully accelerate the projects of our clients.

As Project Manager I am responsible for the day-to-day management of MDMC across the 5 universities, ensuring deadlines and deliverables are achieved across the consortium while proactively managing close working links with key internal and external stakeholders.

I am a registered nurse with med-tech, clinical trials, and preclinical testing experience, including developing Thiel embalmed cadavers for preclinical research and training. I am driving the Tayside Innovation MedTech Ecosystem (TIME), introducing new healthcare technologies.

As a research technician with 12 years experience in surgical simulation, I provide the expertise required to deliver cadaveric simulation models. With an emphasis on imaging, I deliver projects enabling pre-clinical testing of medical devices.

I am a Technology Specialist with 10+ years of experience in precision manufacturing. My role is to assist in the manufacturing of new medical devices.

My role in MDMC is to provide a link with opportunities and equipment to the highly active medical devices community at the University of Glasgow. My own manufacturing specialism is in mesoscale fabrication, with microultrasound devices as a specific target.

I lead the research group on Sensors and Instrumentation at the School of Engineering, Robert Gordon University, providing particular expertise on manufacturing of biosensors and related instrumentation.

As a senior statistician within the statistical team, I provide expertise of the developmental pathway of medical devices, particularly study design. I also sit on the MDMC Executive Group to represent the ECTU in providing statistical support to the project.

I am a medical statistician specialising in clinical trials, with previous experience as a consultant statistician in the life sciences industry. I have expertise in the design and conduct of medical device trials, both in academia and industry, including regulatory knowledge.

I have a long career in nurse education at the University of Edinburgh becoming Professor of Student Learning (Nurse Education) in 2012 and holding key responsibilities in the undergraduate and post graduate nursing programmes.

Professor Lis Neubeck is a cardiac nurse and Head of the Centre for Cardiovascular Health at Edinburgh Napier University. Her research includes management of atrial fibrillation and digital health.

I am the Clinical Director at the Large Animal Research and Imaging Facility at the Roslin Institute and in this role organize and manage any safety and efficacy studies required: i) in the development of medical devices and ii) to meet any subsequent regulatory requirements.