Mark works closely on the project management and development of medical devices, from early stage technical assessment of potential technologies/devices through to industrialisation. As head of quality engineering, he is responsible for ensuring that our internal operating systems reflect current best practice and are in compliance with ISO 13485:2016.
“It’s vitally important that we have a clear understanding of our clients’ vision and that this is translated into verifiable requirements. Occasionally this vision is unclear or ambiguous, in which case we can support our clients in the development of their vision and requirements. As the project progresses things change and we must be flexible and clearly communicate the implications and options associated with the changing vision and requirements.”
Since joining Team in 1996, Mark has worked with start-up and multi-national companies on the development of medical devices including implants, surgical instruments and drug delivery systems. More recently, Mark’s focus has been the technical assessment and development of auto-injectors.