1. MOAZ HEWEDY
Address: 3 Peace St. Edison, NJ, 08820 Mobile: +1(848) 260.9207 E-mail: m.hewedy10@gmail.com
OBJECTIVE
To contribute my skills in simulation, electronics and programing skills to interesting projects, challenging problems, and creative solutions in the field of
Biomedical, Biomechanical and Bioinstrumentation Engineering.
EDUCATION
New Jersey Institute of Technology, Newark, NJ
Newark College of Engineering, Bachelor of Science in Biomedical Engineering
Graduation Date: May 2015, GPA: 3.2
WORK EXPERIENCE
Abbott Point of Care (Princeton, NJ)
Engineer (Instrument Operation) September 2015 – Present
❖ Modified Procedures to ensure that the quality of the final product is up to standard with GMP regulations.
❖ Working to procure equipment for 4 different repair centers that Abbott is trying to start up across Europe and Asia.
❖ Working with outside vendors to procure the equipment and have it assembled, calibrated, RoHS compliant and meet all requirements to have the
repair centers ready to go.
❖ Have procured almost 70% of all the equipment Abbott is currently using to run their production line.
❖ Working with various vendors to procure the equipment and bring it in house, validate the equipment, assemble the equipment, and calibrate it.
❖ Constantly working to procure more equipment as needed to prevent any hindrances on production.
❖ Worked with vendors to meet equipment needs for production
❖ Worked with Engineers on various equipment
❖ Maintain an active spreadsheet of equipment in house and affirming that it is up to date to maintain the flow of production, and prevent any
hindrances due to calibration or engineer needs for equipment
❖ Responsible for preparing four repair sites in four different countries by building, assembling, and supplying equipment in preparation for
production in Europe, and Asia.
❖ Responsible for getting the Darwin 500 production line running by assembling and preparing all the equipment required for production of the new
product, through means of assembling them in house or out sourcing them to vendors and managing vendors to meet deadline and the required
quality of work.
❖ Build various equipment such as Laser Gauge Fixture from the mechanical and electrical aspect
❖ Managing an excel sheet of all equipment required to for the start of the production line and working towards attaining all the components required
to assemble all equipment, calibrate them, and have them setup on the production floor before launch date
❖ Responsible for assembling equipment for the Dragonfly project for testing at Singapore; through building equipment and outsourcing them.
❖ Run Gauge R&R tests on equipment and supervised operators as they conducted the test and affirming they conduct the test properly.
❖ Conducted verification of processes and procedure and wrote verification reports that consisted of assessment reports, facility, utility, equipment
reports.
❖ Determine the material specifications for replacement product for obsolete equipment to continue production without any hindrance or obstruction
of production
❖ Determine the drawing associated with equipment that needs to be outsourced or made for the Dragonfly project.
❖ Updating Procedures to meet FDA standards and to ensure that all standards in the process are met with clarity.
❖ Run Experimental Validation and Verification Design tests to determine if equipment being used meets the intended use of production
Stryker (Mahwah, NJ)
Biomedical Engineering (Advanced Operations) Co-op January 2015 – May 2015
❖ Responsible for leading and maintaining communications between Stryker and Global Vision to determine the requirements that the engineering
team needs from the new system to be implemented, that’s besides participating in the validation process to assure the acceptability of the system in
Stryker’s policies and regulations.
❖ Developed 10s of designs concepts for better development of packages to preserve the products during shipping without any damage while
conserving sterility, affirming that the design is universal for all different sizes of Femoral Heads & Sleeves and Global Cup produced by Stryker, as
well as customer friendly.
❖ Plan a high level structured schedule for the processes encompassing every step from concept to launch, in addition to managing various vendors
that perfects the design to reduce company production and manufacturing expenses.
❖ Established a training binder and a master validation list to enhance the engineering team’s performance during FDA inspection processes by at least
50 percent. The “Q12” enhances the performance of various teams in Styker under cases of FDA inspections in the nation, in Ireland, and France as
well.
❖ Assist the team, from a marketing perspective, by creating a periodical event that will bring nurses and surgeons into the plant and provide them
with a demonstration of the entire process of how the implants are made, how it’s validated, and how it’s packaged and shipped, to obtain feedbacks
that would enhance the company’s sales and becoming more costumer friendly by combining our goals with our customers.
❖ Designed and maintain multiple 3D models, detailed drawings, and assembly drawings of the implants and the packaging using Creo
❖ Conduct laboratory tests and calibrations to determine product’s sterility, such tests include tensile, bubble, and dye testing.
New Jersey Institute of Technology (Newark, NJ)
Capstone Graduation Project January 2014 – January 2015
❖ Start with basic requirements or concept, assist with development of a complete mechanical and electrical design packages, including modeling,
analysis, building, and testing as required to build a knee rehabilitation device (Optiswing).
❖ Collect, interpret, and use publications, documents, and designs prepared by other disciplines, experts, vendors, or outside sources and incorporate
them into the design of the product.
❖ Prepare and present reports of conducted market research of competitors and producers of the product, and generate customer needs of the device, to
generate design drawings and related documentation.
2. MOAZ HEWEDY
Address: 3 Peace St. Edison, NJ, 08820 Mobile: +1(848) 260.9207 E-mail: m.hewedy10@gmail.com
❖ Work with team and faculty members to generate innovative designs with manufacturability in mind, and this includes assistance with physical
assembly or construction of some components and/or systems and/or test set-ups.
❖ Produce detailed solid models of components and/or systems that can be used for parametric analysis, as well as for built-to-print engineering
drawings.
❖ Write requirement papers, test plans and protocols such as Gauge R&R, verification, user guide manuals for ways to troubleshoot and develop the
product, develop a test plan to test the system and product to confirm ease and accuracy of its operations.
LEADERSHIP EXPERIENCE
NJIT Muslim Student Association (MSA)
President January 2014 – January 2015
❖ Planned the association’s strategies to outreach, connecting, and communicating with students and organizations.
❖ Managed the relationships and coordination between Eboard members of the organization.
❖ Engaged students in activities and events to get them connected to the campus community.
❖ Established and maintained relationships with various organizations on and off campus.
❖ Inspired various organizations to support our humanitarian and diverse causes on and off campus.
❖ Coordinated efforts with the treasurer to develop plans for costs of the events held by the association as well as fundraise 10,000 dollars and
maintain them for budget.