 Position included but was not limited to investigating failures of device and components in the field to ensure safety, effectiveness and compliance are met according to United States FDA 21 CFR and ISO 13485 Provided analysis and trending data on all complaints Applied Risk management techniques as necessary Aided in minimizing exposure to product liability lawsuits Utilized technical background to understand functionality and intended use of complex medical devices Worked and collaborated daily with a cross functional team to increase efficiency and understanding of different situations Ensured quality system in place was effectively implemented and maintained

- Tested and built a device to be implemented in the Great Lakes region of Africa that utilized the Internet of Things to monitor flow and turbidity of well-pump water and send all collected data to a cell phone for further processing- Project required defining specifications, a detailed budget, prototyping, testing, and manufacturing all necessary components- Assumed the lead role on the assembly and integration of the electrical/power subsystem- Developed understanding of testing protocols and procedures- Wrote, proof read, and edited technical documents required for design and test reviews- Maintained consistent lines of communication between team members and project director- Gained experience in the full start to finish product design process

- Performed value engineering measures on technical projects- Participated in cost optimization reviews- Developed a bill of materials for projects- Communicated with clients on a daily basis- Participated in volunteer opportunities