Interface Engineer

Interface Engineer

Responsibilities:

• Participate actively as part of the dynamic software development team.
• Develop and manage communication interfaces for medical devices using serial protocols (RS-232, RS-485, etc.) to ensure reliable data transmission between devices and healthcare systems.
• Identify, diagnose, and resolve problems in serial communication between medical devices and software systems, ensuring minimal downtime and data integrity.
• Conduct thorough testing of serial interfaces to ensure accuracy, reliability, and compliance with medical device standards and regulations.
• Create detailed technical documentation, including interface specifications, workflows, troubleshooting guides, and user manuals.
• Innovate with ideas for improving the solution.

Requirements:

• Possess a recognized Degree in Computer Science/Information Technology or equivalent.
• 3+ years of experience in developing and integrating medical device interfaces, healthcare IT, or medical software development.
• Programming experience in Visual Basic, VB.Net, ASP.Net, or C#.Net.
• Database handling experience in Oracle.
• Experience in Serial Communication Protocols:
• RS-232, RS-422, RS-485: Proficiency with serial communication standards used in medical devices.
• Modbus, UART, I2C, SPI: Familiarity with these serial communication protocols for data transfer between devices and systems.
• Skills in debugging issues in the hardware-software interface, particularly when dealing with serial communication problems (e.g., signal integrity, noise issues, timing problems).
• Experience with the integration and testing of serial communication between medical devices and other systems, ensuring data integrity and reliability.
• Experience with integrating medical devices that rely on serial interfaces into healthcare systems.
• Knowledge of data parsing and handling to ensure seamless communication between devices.
• Experience with communication protocols (e.g., HL7, DICOM, FHIR) used in healthcare systems.
• Familiarity with medical device standards, regulations, and certifications (e.g., FDA, CE Mark, ISO 13485, IEC 62304).
• Very strong verbal and written communication skills.
• Ability to work under pressure.