Director

• Jan 2017 - Present

Viewing Facility Manager

• Feb 2022 - Present

Our state of the art viewing facility consists of a viewing room and a usability lab (respondent room) with a one way mirror adjoining the two rooms. The facility is fitted with the latest HD recording equipment, is fully sound-proofed and can accommodate a range of different use environments. Both the viewing room and usability lab are fitted with specialised lighting which can be dimmed or brightened to suit your lighting environment needs. The Lab is available for hire as a standalone viewing facility (viewing room and usability lab) with a manned reception to welcome all participants and assist with consent capture. HD video and audio recording is included in the rate of hire and refreshments are also provided for you and your participants. https://humanfactorscentre.co.uk/human-factors-lab Outside of the lab, there is a large lounge which serves as a participant waiting room and/ or additional working space. Our reception is manned at all times and our staff prepare your recordings each day in-line with your desired respondent coding.

Principal Engineer

• Jul 2019 - Jan 2022

Helped clients to develop the next generation of medical devices throughout the entire product development process. Worked in all capacities of engineering, mechanical, electrical, software, human factors as technical lead and project manager making strategic decisions to ensure a successful project outcome. Helped clients to develop the next generation of medical devices throughout the entire product development process. Worked in all capacities of engineering, mechanical, electrical, software, human factors as technical lead and project manager making strategic decisions to ensure a successful project outcome.

Senior Consultant - Mechanical Engineering

• Jul 2017 - Jun 2019

Senior Consultant in the Mechanical Engineering group at PA Consulting

Consultant - Mechanical Engineering

• Jan 2016 - Jul 2017

Mechanical Engineer

• Mar 2015 - Jan 2016

At Olympus I was responsible for developing new products within the R&D team. I worked on a concept product from the early stages. This has entailed gathering and evaluating customer requirements, generating concepts and conducting site visits to local hospitals to present these concepts. Also while at Olympus I was called upon to assist in preparation for an FDA inspection. This required me to review several Design History Files of older products with the intention of finding and remediating errors. This required me to have a comprehensive knowledge of both internal procedures and external regulations such as 21 CFR, ISO 14971 and ISO 13485 to name a few. As a result of this work, I have a complete understanding of what is required in a medical device manufacture, to ensure that both a compliant product and documentation set is produced, at the end of a project and what is required after project completion to ensure compliance is maintained.

Mechanical Engineer

• Oct 2012 - Mar 2015

At Elekta I was part of their revolutionary project to create a new type of linear accelerator for use in radiation therapy. The goal of this project was to combine the most sophisticated Linac in the world with an MRI machine. This project was run in conjunction with Philips and was very challenging, enjoyable and exciting. I personally was given ownership over four subsystems and was responsible for designing and delivering the prototypes to schedule. My team of engineers, designers and I accomplished the completion of these subsystems and were a major part of effort to build the first prototype system at UMC hospital in Utrecht. This involved extensive communication within the R&D department and other parts of the business as well as with the hospital staff at UMC. Working at Elekta allowed me to hone my leadership skills and learn a great deal about product creation, prototyping, engineering design and analysis and project implementation.