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Tier-1 employer and metro location increase competition, but senior regulated testing narrows applicant pool.
Heavy regulatory, HIL, and hardware testing requirements limit cross-industry transferability.
Explicit 12–16 years and required regulated automation, HIL, and hardware debugging increase filtering strictness.
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Develop, maintain, and execute scalable automated testing frameworks and test suites for advanced software systems in medical devices.
Collaborate with software, systems, hardware, and quality engineering teams to ensure compliance with product and regulatory requirements.
Analyze workflows for quality risks and lead continuous improvement initiatives in software verification and validation processes.
Bachelor’s degree in Computer Science, Software Engineering, or equivalent.
12 to 16 years of relevant experience in software test automation and system-level testing.
Strong programming skills in Python, C#, or C++ and experience with automation frameworks and tools.
Experience with medical device software testing, hardware debugging tools, software verification/validation, and regulatory compliance requirements.
Experienced in designing and executing complex automated test strategies for regulated medical device software and hardware integration.
Comfortable working cross-functionally in Agile/Scrum teams involving software, hardware, and quality assurance domains.
Skilled in managing multiple hardware/software test configurations and maintaining quality management system test documentation and processes.