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Key skills for this role
Bachelor’s or master’s degree in computer science,
Software Engineering, Electronics Engineering, Instrumentation Engineering, Biomedical Engineering, or a related discipline.
5–12 years of experience in software development, validation, automation, or manufacturing engineering within a regulated industry.
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Familiarity with regulated product development processes and quality management systems.
Knowledge of scripting languages (Python) for automation and test utilities.
Experience with Qt-based GUI applications and Windows desktop application development and testing.
Knowledge of data acquisition systems (DAQ), hardware interfaces, and system integration.
Experience in medical device software validation, verification activities, and documentation within a regulated environment. Good to Have
Experience with test fixtures, custom hardware setups, and automated test benches.
Experience supporting manufacturing test systems and production automation.
Familiarity with medical device standards such as IEC 62304 and related verification practices.
Experience with defect tracking, requirements management, and traceability tools.
Experience with CI/CD and automated software validation pipelines.
Understanding Computer Vision , object tracking concepts, coordinate conversion, and mathematical algorithms.
Global leader in medical technology and healthcare solutions.
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Senior · 5+ years experience
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