Base Career helps you apply smarter for this job.
Key skills for this role
Bachelor’s degree in computer science software engineering or equivalent with 12 to 16 years of relevant experience. Bio-Medical expertise will be preferred.
Strong programming experience in languages such as Python, C# or C++.
Experience testing on Web / Desktop Applications.
Experience with UI automation tools such as Ranorex, Appium, Katalon, or Squish.
Experience designing and implementing test automation frameworks.
Skip the repetitive application forms
Install the Base Career Chrome Extension and autofill job applications across major job boards with your profile.
Trusted by over 500,000 job seekers on Base Career
More from this employer
Canberra, AUS
Brampton, CAN
Medtronic is seeking a Regulatory Affairs Specialist for an 18-month contract to manage medical device regulatory submissions, product maintenance, compliance activities, and Health Canada interactions. Candidates need a
Brampton, CAN
Medtronic is seeking an Associate Regulatory Affairs Specialist for an 18-month contract to support medical device submissions, product changes, regulatory compliance, and agency communications. A baccalaureate degree is
Canberra, AUS
Perth, AUS
London, GBR
London, GBR
London, GBR
London, GBR
Brampton, CAN
Brampton, CAN
Experience with software verification and validation processes.
Familiarity with software development lifecycle methodologies.
Experience collaborating with cross functional engineering teams.
Experience working in Agile or Scrum development environments.
Experience with hardware debugging tools such as oscilloscopes or function generators.
Ability to manage, track and upgrade multiple hardware and software configurations.
Experience using version control systems such as Git.
Familiarity with test management tools such as Polarion, TestRail, JAMA, or TFS.
Strong analytical, debugging, and problem-solving skills.
Excellent documentation and communication skills.
Quality Management System – Test Planning, Strategy.
Ability to work with QA to ensure testing meets Quality and Regulatory needs. Nice to have:
Experience with QT/QML.
Experience working with Linux environments is preferred.
Experience in medical device software development or regulated environments.
Knowledge of medical device standards such as IEC 62304 and FDA software guidance.
Knowledge on CI-CD Workflow. Docker.
Knowledge of AI tool usage. Like Co-Pilot, Cursor.
Experience with system‑level testing of integrated hardware and software platforms.
Global leader in medical technology and healthcare solutions.
Visit company websiteJobs and hiring trendsFull-time
Senior · 12+ years experience
Hybrid
Apply faster on company sites with our extension.