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Tier-1 brand and metro location increase applicant density, but specialized regulated test-automation narrows the pool.
Strong regulated medical-device and hardware-integration requirements limit cross-industry transferability.
Explicit 5–12 years, regulated-medical validation, and specific Qt/DAQ/test automation skills required.
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Develop and maintain automated manufacturing test software solutions including Qt-based GUI applications and test automation frameworks.
Collaborate with cross-functional teams to integrate software with hardware systems such as data acquisition, sensors, and manufacturing equipment, ensuring quality and regulatory compliance.
Drive software validation, verification, and documentation activities within a regulated medical device manufacturing environment to improve test coverage and manufacturing throughput.
Bachelor’s or master’s degree in Computer Science, Software Engineering, Electronics Engineering, Instrumentation Engineering, Biomedical Engineering, or related discipline.
5–12 years of experience in software development, validation, automation, or manufacturing engineering within a regulated industry.
Experience with Qt-based GUI application development, Python scripting for automation, and Windows desktop application testing.
Familiarity with regulated product development processes, medical device software validation, and quality management systems.
Experienced in regulated medical device manufacturing environments with strong knowledge of software validation and quality compliance.
Technical expertise spanning software development, hardware-software integration, and manufacturing test automation, including data acquisition systems and sensor integration.
Capable of leading continuous improvement initiatives in manufacturing test efficiency and defect resolution with a detail-oriented, process-driven approach.