Danial Al Hamoud Email & Phone Number

Saudi Arabia

Fort Mill, South Carolina, United States

• Perform repair, quality actions, preventative maintenance and troubleshooting activities on high-risk medical devices, which includes ventilators, pumps, and occluders.
• Comply with all Quality, ISO (International Organization for Standardization – Regulatory requirements for Medical Devices), and GMP (Good Manufacturing Practices – quality system for products regulated by FDA).
• Complete timely and accurate administrative duties such as documentation and expense reports through an Internal ticketing system.
• Ensure customer satisfaction through quality workmanship, documentation, and customer communication.
• Maintain inventory of service parts, test equipment, documentation, and tools.

Rock Hill, South Carolina, United States

• Perform the set-up, test, and troubleshooting of System components and assemblies of a variety of 3D printing machines
• Design 3D-printed fixtures to assist with installation of parts in addition to being used as a specialized test equipment.
• Follow established work procedures on routine work in order to ensure consistent quality.

Richmond, Virginia

• Documented all the beds and stretchers in the hospital into the system of the company to develop a new list with the exact amount that exist in the hospital.
• Performed preventative maintenance, and electrical safety tests to ensure the quality of equipments before approving of its Patient Ready status.
• Checked the functionality of equipments and Identified mechanical/electrical issues before repairing them.

Columbia, South Carolina Area

• Troubleshot mechanical and software errors to ensure that the VIM can run a full consistent cycle.
• Developed test methods for verifying the weighing station, and the camera system of the VIM machine.
• Developed requirements and specifications for weight, and twist-off torque values for the vials.
• Generated and executed commissioning and qualification protocols for VIMs (PDP, O&M Manual, SOP, IQ, OQ, PQ) before reviewing documents for cGMP compliance.
• Contributed to department efficiency initiatives by saving $432 per shift while keeping the same vial inspection output.
• Prepared a 24-page report on the validation summary that includes goals/objectives, methodology, results, and limitations.