Research & Development•Performed extensive scientific data modeling and curve fitting.•Worked data analysis on raw UV Spectrophotometric data using the Beer-Lambert Law.•Developed mathematical functions to convert raw UV Spectrophotometric data into meaningful molecular concentration measurements for different solutions.•Created experimental procedures to quantify manufacturing variances in wavelength of UV LEDs and in optical physics of sample analysis trays.•Produced mathematical functions to automatically compensate for manufacturing variances in wavelength of UV LEDs across thousands of devices and the optical physics of thousands of sample analysis trays.•Constructed calibration method that improved product device accuracy by more than 50% and created new production and quality metrics for monitoring manufacturing.•Performed mathematical model validations based upon empirical data.DesignDesigned and engineered the following for various projects: •Consumer products through concept, prototype, manufacture, and production phases. •3D Modeled handheld consumer electronics parts with AutoDesk Fusion 360. •Parts for ABS, PC, and Topas plastic injection molding. •Optical lenses for focusing UV light. •Parts with fluidic microchannels for use with UV Spectrophotometry •Cardboard and foam packaging. •2D technical drawing packages for manufacturing and assembly.Performed Design for Manufacturability analysis.Collaborated with Electrical Engineers on component selection to guarantee fit/functionality.Collaborated with Printed Circuit Board layout designer to ensure proper component placement.Submitted mechanical drawing packages to multiple manufacturers for quotes.Created CAM tool pathing using AutoDesk Fusion 360.Generated and edited G-Code and M-Code for CNC Mill to produce prototypes.Verified design elements and performance using 3D printed and CNC Milled prototypes.

Designed and modeled surgical instrument accessories using SolidWorks.Created manufacturing drawings.Performed tolerance stack up analyses.Performed Quality Control inspections.Obtained CE Mark registration for Class I Medical Devices.Generated Risk Analysis reports.Familiar with 21 CFR 820 and MDD 93/42/EEC