LabVIEW Engineer — Medical Device Test Equipment

Innovative Health LLC; Scottsdale (AZ); On-site; USD 80,000 - 120,000; Full time

Job summary

Innovative Health LLC in Scottsdale is seeking an Electrical Engineer to develop, test, and maintain specialized equipment for medical devices. You will design LabVIEW-based test systems, analyze data, and ensure compliance with quality and regulatory standards.

The role requires 3–5 years of electrical engineering experience focusing on test equipment, strong LabVIEW skills, and familiarity with FDA/ISO 13485 guidelines. Collaboration with QA and regulatory teams is essential.

Qualifications

• Bachelor's or master's degree in Electrical Engineering.
• 3–5 years experience focusing on test equipment for medical devices.
• Proficiency in LabVIEW and NI hardware.
• Strong understanding of electrical circuits and signal processing.
• Familiarity with FDA and ISO 13485 regulatory requirements.
• Excellent problem-solving and communication skills.
• Experience with Python or C/C++ is a plus.

Responsibilities

• Design and develop test equipment for medical device verification.
• Develop, debug, and maintain LabVIEW applications for automated testing.
• Perform electrical and functional testing and analyze results.
• Calibrate and maintain test equipment; keep calibration records.
• Collaborate with QA and regulatory teams on test plans and documentation.

Skills

LabVIEW programming

NI hardware

Python

C/C++

Signal processing

Electrical circuits

Regulatory knowledge

Team collaboration

Education

Bachelor's or master's degree in Electrical Engineering

Tools

LabVIEW

Job description

Innovative Health LLC in Scottsdale is seeking an Electrical Engineer to develop, test, and maintain specialized equipment for medical devices. You will design LabVIEW-based test systems, analyze data, and ensure compliance with quality and regulatory standards.

The role requires 3–5 years of electrical engineering experience focusing on test equipment, strong LabVIEW skills, and familiarity with FDA/ISO 13485 guidelines. Collaboration with QA and regulatory teams is essential.