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Staff Software Test Engineer

Staff Software Test Engineer

CompanyInsulet Corporation
LocationActon, MA, USA
Salary$118500 – $177750
TypeFull-Time
DegreesBachelor’s
Experience LevelExpert or higher

Requirements

  • Proficiency in Python scripting with strong debugging capabilities
  • Prior experience in a software testing or software quality assurance team
  • Bachelor’s degree in software engineering, Computer Science, or related field
  • 10+ years of hands-on experience in software quality assurance, preferably in real-time systems within regulated industries; or an equivalent combination of education and experience
  • At least 2 years of experience in a lead or senior QA role
  • Deep understanding of QA principles, software testing best practices, and quality metrics
  • Practical experience with modern development and QA tools (e.g., version control, CI/CD, test management)
  • Proven track record in developing and executing comprehensive software test protocols for complex systems

Responsibilities

  • Work closely with the software development team to identify improvements
  • Influence the requirements definition and software design to maximize testability
  • Oversee and influence development of test objects to meet needs of protocol
  • Develop and extend protocols and plans as device features evolve
  • Participate in product design reviews
  • Represent SQA in the core team meetings
  • Creating and executing test plans, test designs and test cases and generating test reports for them
  • Creating and updating Trace matrices between requirements and Tests
  • Provide direction/guidance to the QA team
  • Remove blockers for the SQA team
  • Design the path forward for the team
  • Work with the scrum Master to identify way on how deprioritize ‘Nice to have feature’ to pull in timelines, if needed
  • Keep track of the Testing board and tools inventory for the team
  • Performs other duties as required

Preferred Qualifications

  • Experience supporting products from prototype through FDA 510(k)/ISO submission and commercialization is preferred
  • Familiarity with relevant standards and regulations (e.g., IEC 62304, ISO 14971, FDA regulations) is a strong plus