● 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) regulations.● 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.

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.

• 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.

• 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. • Conducted project review meetings within the team, with management and with the manufacturer of the VIMs.• Performed training for QA staff and production employees on the 3 VIMs.