Responsibilities focused around managing numerous small design projects of surgical instruments and implants from concept development to delivery to the end user. Activities performed within these projects included designing and generating CAD models and associated drawing in both Solidworks and Pro/Engineer Wildfire, analyzing potential risks of the product, and conducting validation testing and reporting. These activities were successfully accomplished through the coordination of a cross-functional team, including 3rd party manufacturing vendors. In addition, time was allotted to performing and documenting testing as part of a response to an Additional Information request from the FDA for 510(k) notification of a new product.

Instruct Purdue first-year engineering students in the understanding of basic engineering fundamentals, including basic statistics, the principal of design, flowcharting, and computer programming. In addition, conduct open office hours to facilitate the students' comprehension of class topics and guide their development of a logical thought process through open-ended problems.

Responsibilities focused around managing numerous small design projects of surgical instruments and implants from concept development to delivery to the end user. Activities performed within these projects included designing and generating CAD models and associated drawing in both Solidworks and Pro/Engineer Wildfire, analyzing potential risks of the product, and conducting validation testing and reporting. These activities were successfully accomplished through the coordination of a cross-functional team, including 3rd party manufacturing vendors. In addition, time was allotted to performing and documenting testing as part of a response to an Additional Information request from the FDA for 510(k) notification of a new product.

As design lead of a cross-disciplinary project team, composed and completed Design History File documentation including risk assessments, traceability matrices, clinical evaluations, and test protocols in order to successfully complete these design deliverables to FDA and ISO MDD requirements. Additionally, performed risk management for multiple projects to ensure acceptable levels of safety for the end users and conducted functional relationship analyses to evaluate the mating fits for designed devices.