▬ Performed manual assembly and installation of subassemblies for Alinity s instrument per manufacturing and quality procedures. ▬ Created electronic records of manufacturing documents in line with documentation standards of Quality system. ▬ Performed verification tasks during manufacturing cycle to maintain the effectiveness of the Abbott Quality Management System per ISO and FDA regulations.▬ Performed system level functional test, failure analysis and troubleshooting of technical system on Alinity s blood screening instrument to determine effectiveness of product specifications▬ Identify, document and report non-conformances found during assembly and functional test of instruments▬ Collaborated with a multidisciplinary team to identify and solve design issues of instrument

▬ Performed inspection, repair and preventative maintenance for Alaris System including: infusion pumps, syringe pumps, PCA pumps, and PC monitors▬ Performed repair on a Giraffe Omnibed Infant Warmer▬ Assembled and networked Capsule Vital Signs monitor▬ Utilized SNOW (Service Now) software to close work orders

▬ Performed research related to robots used in rehabilitation applications. ▬ Examined use of mobile robots to enhance STEM education for K-12 schools through the context of play ▬ Researched impact of gun violence as the leading cause of violently acquired spinal cord injuries (VASCI) within the black community ▬ Examined experience of black men with violently acquired spinal cord injuries (VASCI) within both the black community and the disability community.▬ Developed engineering education curriculum for local Rochester K-12 schools involving block programming and JavaScript. ▬ Wrote paper abstract on A Novel Approach to teaching STEM and Disability Studies to K-12 students ▬ Created 5 minute video presentation to present at the International Conference of the IEEE Engineering in Medicine and Biology Society (EMBC 2020).

English Language Center ▬ Facilitated the transfer and organization of about 850 student files into a new database called OnBase

Biomedical Engineering Department▬ Implemented a method for improving blood-contacting medical devices which cause blood cell damage▬ Standardized and documented manufacturing process in Standard Operating Procedures▬ Showcased research results at RIT Undergraduate Symposium 2018

Biomedical Engineering Department▬ Revamped and optimized the design and manufacturing of point-of-care device▬ Reduced manufacturing cost by 80%▬ Established documentation for past and present design iterations of point-of-care device▬ Developed an AutoCAD blueprint drawing of an academic research laboratory

Higher Education Opportunity Program (HEOP)▬ Coached students in subjects such as General & Analytical Chemistry to better understand the course content.

▬ Developed products for a collaborative R&D project involving multiple laboratories. Tracked the progress of study▬ Manufactured product prototypes for troubleshooting of external laboratory assays▬ Managed and documented Design Control process for one pipeline project. ▬ Built pipeline products in the Design Control phase. ▬ Performed value assignment of raw materials using Digital Droplet PCR (ddPCR)▬ Analyzed data for value assignment and quality control release of raw materials and products▬ Executed nucleic acid purification on QIAcube HT System, QIAcube System and Promega Maxwell RSC System▬ Performed Real Time PCR on ABI7500 FAST System and Focus 3M Integrated Cycler

▬ Devised solution to prevent the re-occurrence of a non-conformity using the CAPA system▬ Updated records of Document Change Requests▬ Performed daily verification tasks throughout manufacturing cycle to maintain Quality Management System. ▬ Performed root cause analysis for non-conformities that result in Corrective Action Preventative Action (CAPA) per ISO 13485▬ Facilitated document control and the routing of Document Change Requests▬ Incoming Inspection approvals for raw materials▬ Updated records of Certificate of Analysis (CoA) for Catalog and Custom products on the website▬ Performed QA Batch Record release for value assignment of raw materials▬ Issued batch records for the manufacturing of Catalog and Custom In-vitro Diagnostic (IVD) ▬ Processed the approvals of vial and kit labels, including CE marked labels

▬ Manufactured single and multi-analyte In Vitro Diagnostic (IVD) verification panels per cGMP and ISO 13485▬ Developed and applied labels to products per Quality Management System▬ Tested products for quality control and assay validation on ABI7500 FAST and In-House assays

Discrete Microfluidics Laboratory▬ Investigated the effect of the Coffee Ring Phenomenon in colloidal material▬ Controlled particle transport in colloidal droplet deposition using an electrode▬ Monitored colloidal material with Ramé-hart contact angle goniometer▬ Presented research results at RIT Undergraduate Symposium 2016

RIT Telefund▬ Contacted alumni and parents to build rapport, update demographic information and acquire gifts for the Development Fund, a financial reserve used to support and improve department facilities and overall student life▬ Informed University supporters of new events happening on campus