SUMMARY
Over two years of industry experience with a track record of successfully completing projects with well-developed skills in computer-aided design software, technical drawings, data analysis, technical memo writing, engineering design, and product development.
EDUCATION
University of Central Florida (UCF), Orlando, FL
BS in Mechanical Engineering (BSME), May 2012
EIT Certificate #1100017714, April 2013
WORK EXPERIENCE
Product Engineer, August 2015 - Current
Boeing Defense, Space & Security, Systems Engineering Department - Ridley Park, PA
• Worked with a cross functional team of engineers to process, evaluate, and classify engineering change requests (ECR) to the H-47 Chinook Tandem Rotorcraft.
• Responsibilities include:
o Run Change Implementation Team (CIT) meetings for both Airframes and Electrical Wiring departments.
o Evaluate the CR’s impact on fit form and function of component, to designate change as Class I or Class II.
o Determine if CR impacts multiple Integrated Product Teams (IPT), to designate change as Class I or Class II.
o Enter changes into Teamcenter, create change schedule, and coordinate signature signoffs from multiple heads of departments to approve CR.
o Create guidance documents to standardize the change process across different CITs.
• Highlight: Received invitation to Principles of Flight workshop offered at Boeing.
Product Development Engineer, April 2015 - July 2015
Johnson & Johnson, Biomaterials Department - West Chester, PA
• Ensure that Technical Files for Class I, IIa, and IIb meet the requirements set forth by the Medical Device Directive (93/42/EEC) so that they can be released in the European Economic Area (EEA) with CE marking.
• Responsibilities include:
o Evaluate implant’s conformance to ISO 14630 Non-active Surgical Implants-General Requirements.
o Create and update Design Clinical Risk Management Matrix.
o Create European instructions for use (IFU) to include: indications and contraindications established on American IFU, and any additional language required by Medical Device Directive for labelling.
• Highlight: Completed corporate integrity agreement (CIA) training required by the Office of Inspector General.
Product Development Engineer, March 2014–March 2015
Zimmer Biomet, Trauma Department - Warsaw, IN
• Involved in the remediation of Design History Files, for trauma implants and US Class II instruments, to ensure compliance with 21 CFR 820.30 (Design Control) FDA’s Quality System Regulation.
• Responsibilities included:
o Evaluated changes to implant’s prints, surgical techniques, engineering specifications, and package inserts, to determine if the implant’s performance or safety was altered.
o Created technical memos to provide verification/validation for changes.
o Documented and evaluated risk management activities (DFMEA).
o Developed protocols and procedures for functional r...
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