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Strong employer brand and metro location, but niche medical device testing reduces general applicant density.
Requires regulated medical device testing, hardware and IEC 62304 knowledge, limiting cross-industry transferability.
Explicit 12–16 years and mandatory regulated medical device testing skills increase filtering rigidity.
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Design, develop, and maintain automated testing frameworks for complex medical device software systems in the Affera Mapping and Ablation System team.
Collaborate with software, systems, hardware, and quality engineering teams to ensure software meets product and regulatory requirements including medical device standards.
Analyze workflows and software to identify quality risks, develop automated test strategies, and support software verification, validation, and continuous improvement processes.
Bachelor’s degree in computer science, software engineering, or equivalent.
12 to 16 years of relevant experience in software test engineering, preferably in biomedical or medical device domain.
Programming experience in Python, C#, or C++. Experience with UI automation tools such as Ranorex, Appium, Katalon, or Squish is mandatory.
Experience with software verification and validation processes, Agile/Scrum methodology, and hardware debugging tools.
Experienced in developing and managing scalable automated test frameworks for regulated medical device software.
Comfortable working cross-functionally with software, hardware, systems, and quality engineering teams in Agile environments.
Demonstrated ability to ensure compliance with quality management systems and regulatory standards such as IEC 62304 and FDA software guidance (preferred but not mandatory).