Founder
Current
President
Vice President Of Internal Programing
Process Development Intern
Helped develop and standardize an efficient process to transition production and development-level product lines to a new facility while consulting Master Validation Reports to stay within FDA regulations and customer quality agreementsCreated a project transfer schedule consisting of product lines, infrastructure, and personnel which governedUtilized cross-functional communication to execute the move while maintaining ISO 13485-level documentationCompleted the move on time saving the company $320,000 in facility leasing costs
Operations Intern
Increased the output of a detail-oriented work cell for quality testing medical devices by 85%, successfully tested 6000 units in 8 weeks putting the company back in line with demandSet up a training versatility matrix to track training records which increased overall training versatility by 40% thus keeping the business within FDA and ISO 13485 regulations and preventing the line from going downCreated a master production tracking tool used to track output, calculate productivity, and track material shortages for a production line being pushed to production status.Wrote incoming inspection protocols for raw materials and components in a high-compliance medical device environment, ensuring adherence to FDA and ISO 13485 quality standards
Manufacturing Engineering Intern
Increased production by 50% in a three-month window and put the production line on track to double in production by the end of 2022.Studied operational sequences, material flow, functional statements, production line layouts, and project information to determine worker functions and responsibilities.Analyzed PFMEAs and compared them to existing manufacturing procedures. Redlined procedures, improved methods, added clarity, and decreased steps/time.