Mechanical Engineer

• Dec 2021 - Present

R&D Engineer

• May 2018 - Nov 2021

-Design and create semi-automatic manufacturing machines and fixtures with the goal of minimizing total device cost, while maximizing production capabilities.-Implement Process Development Techniques such as DOE, IQ, OQ and PQ.-Perform mechanical design and documented components and sub-assemblies with accordance to company standards.-Interface with other engineering groups and suppliers to develop solutions and resolve technical challenges. -Design and create semi-automatic manufacturing machines and fixtures with the goal of minimizing total device cost, while maximizing production capabilities.-Implement Process Development Techniques such as DOE, IQ, OQ and PQ.-Perform mechanical design and documented components and sub-assemblies with accordance to company standards.-Interface with other engineering groups and suppliers to develop solutions and resolve technical challenges.

Mechanical Engineering Intern

• May 2017 - Aug 2017

• Conducted tolerance loop analysis on already created CAD assemblies verifying and modifying fit suitability of parts• Created Engineering Drawings based on company standard and appropriately documented the changes in company’s database• Conducted DVT (design valuation testing), including drop test, water permeation testing and Radiation Survey, and aptly described the test results in well written reports. • Conducted tolerance loop analysis on already created CAD assemblies verifying and modifying fit suitability of parts• Created Engineering Drawings based on company standard and appropriately documented the changes in company’s database• Conducted DVT (design valuation testing), including drop test, water permeation testing and Radiation Survey, and aptly described the test results in well written reports.

R&D Endovascular Systems Co-op

• Jun 2015 - Jan 2016

• Conducted Performance Qualification (PQ) of Procedures, Operational Qualification (OQ) of Manufacturing Equipment, and Test Method Validations (TMV) and Rationales• Gained Good Documentation Practices and document handling when executing Protocols and Reports for PQ, OQ and TMVs• Conducted Statistical Analysis of Test Data, using Minitab and Distribution Analyzer, needed for the Design Validation of grafts and Original Equipment Manufacturer (OEM) products• Rewrote Manufacturing Procedures and created Training Curriculums to ensure appropriate procedure execution• Worked on Design Master Record and DFMECA (Design Failure Mode Effects and Criticality Analysis)• Reported several Engineering and Labnotebook Studies to support testing procedures when conducting PQs and TMVs• Provided excellent organizational skills and attention to detail when training Manufacturing Personnel to Quality Procedures• Gained testing skills while using Instron Machine and created Instron Programs using Bluehill3 Software• Worked with external companies, such as MicroVision Labs and Medical Device Testing Services, to provide test data support for Design Validation of grafts• Demonstrated good time management when working on multiple projects for two different product lines• Internally Certified by VP of Regulatory for Basic Medical Device Regulations – The FDA Regulations, The European Union & ISO 13485

Sales Associate

• Oct 2012 - Sep 2013

• Demonstrated friendly customer service and patience when resolving all issues in areas including adult and children’s party, item location and item returns• Worked as a team to complete responsibilities, such as opening and closing, merchandise distribution and cleaning of the workplace• Possessed effective ability to learn quickly and competed tasks without needing maager’s direction • Efficiently processed cash, credit card and check transactions while working in stressful situations