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Tier-1 employer and metro location increase competition, but seniority and regulated-medical specialization reduce applicant density.
High—regulated medical device V&V expertise strongly biases against transferable backgrounds.
Strict: 10+ years, automation skills, regulated V&V and specific tech stack required.
Responsible for planning, designing, and executing both manual and automated tests for desktop software applications, ensuring their quality and reliability across multiple platforms including iOS and Android.
Develop and implement automated test scripts using tools and frameworks, with strong programming skills in Python and C#.
Collaborate with internal and external partners to analyze requirements, participate in Agile activities, and conduct software verification and validation compliant with regulatory and quality standards.
10+ years experience in desktop application testing with a focus on test automation.
Bachelor’s degree in Engineering or Technology in Computer Sciences, Biotechnology, Bio-Medical, Electronics, or Electrical Engineering.
Proficiency in programming languages including Python and C# and experience with automation frameworks.
Experience working with test management tools (e.g., JIRA), continuous integration tools (e.g., Gitlab), and knowledge of software verification & validation processes in regulated environments.
Experienced in regulated environments, preferably medical device software or similarly compliant industries.
Comfortable working collaboratively across global sites and teams including Engineering Managers, Test Leads, and V&V engineers.
Skilled in test automation design and execution within Agile/Scrum development processes, with ability to create clear documentation and translate complex requirements into test cases.