Experience

Pathfinder Medical

• United Kingdom
• Medical Equipment Manufacturing
• 1 - 100 Employee

• Project Engineer

  • Dec 2019 - Present

  I manage projects to design and develop two medical devices (a catheter kit and electrical display). Common responsibilities are:• Mechanical design to meet functional and cost requirements• Producing technical drawings/specifications to BS 8888• Managing supplier quality

• Manufacturing Engineer

  • Aug 2018 - Dec 2019

  I worked in R&D to develop a medical device with endovascular applications. This amounted to obtaining a CE mark for the device by meeting MDR requirements. Some examples of work are:• V&V testing (usability, mechanical benchmarking etc.)• Producing technical reports• Process validation



Kewell Converters

• United Kingdom
• Plastics and Rubber Product Manufacturing
• 1 - 100 Employee

• Production Coordinator

  • Mar 2017 - Aug 2018

  I managed a CNC routing batch manufacture service where I coordinated design and production teams while managing client expectations. My responsibilities were: • Production planning • Investigating the root cause of failures and implementing solutions • Process design; reducing costs of industrial processes I managed a CNC routing batch manufacture service where I coordinated design and production teams while managing client expectations. My responsibilities were: • Production planning • Investigating the root cause of failures and implementing solutions • Process design; reducing costs of industrial processes



BTG plc

• United States
• Medical Device
• 200 - 300 Employee

• Research And Development Engineer

  • Jun 2015 - Dec 2015

  I undertook and documented feasibility studies intended to develop early concepts of medical devices. I undertook and documented feasibility studies intended to develop early concepts of medical devices.



BTG plc

• United States
• Medical Device
• 200 - 300 Employee

• Design Engineering Technician

  • Aug 2013 - Aug 2014

  I undertook experimental studies and wrote quality reviewed technical reports to develop a Class III drug-delivery combination product. Some responsibilities were: • Design of injection moulded components • Experimentally evaluating proof-of-principle concepts • Manufacture of medical devices I undertook experimental studies and wrote quality reviewed technical reports to develop a Class III drug-delivery combination product. Some responsibilities were: • Design of injection moulded components • Experimentally evaluating proof-of-principle concepts • Manufacture of medical devices