About The Position

At Clario, we transform lives by unlocking better evidence. As a Software Quality Engineer (V&V), you will play a key role in validating clinical study software to ensure quality, compliance, and reliability. You will collaborate with cross-functional teams to deliver high-quality solutions that support clinical trials and ultimately improve patient outcomes.

Requirements

  • Bachelor’s degree in Information Technology or a related field, or equivalent practical experience
  • 1–3 years of experience in software testing or quality assurance
  • Proven understanding of the software development lifecycle and validation processes
  • Experience designing and executing manual test cases and documenting results
  • Familiarity with defect tracking systems, test management tools, and documentation systems
  • Basic knowledge of test automation and Agile methodologies
  • Strong analytical and problem-solving skills with high attention to detail
  • Effective communication skills in English, both written and verbal
  • Ability to manage multiple priorities, meet deadlines, and work independently or collaboratively
  • Based in or able to work remotely within the United States

Responsibilities

  • Review software specifications and validation documentation to ensure clarity, completeness, and testability
  • Design and develop comprehensive test cases, including functional, integration, and performance scenarios
  • Execute manual test cases, capture test evidence, and manage accurate test data for validation activities
  • Analyze test results, identify defects, and document reproducible issues with clear root cause insights
  • Collaborate with developers and project teams to validate new features and ensure regression coverage
  • Manage the defect lifecycle, including prioritization, retesting, and tracking within bug management systems
  • Maintain and configure test environments, including backend systems and supporting tools
  • Create and maintain validation documentation aligned with SOPs, regulatory standards, and Good Clinical Practices (GCP)
  • Support internal and external audits by preparing and providing required validation documentation
  • Monitor project timelines, risks, and testing progress, providing clear status updates and escalations as needed
  • Contribute to test planning, effort estimation, and coordination across multiple projects
  • Identify opportunities to improve testing processes, tools, and overall quality practices
  • Collaborate across teams, share knowledge, and support onboarding and mentoring of new team members

Benefits

  • Competitive compensation
  • Health, dental, and vision coverage
  • 401(k) retirement plan with company match
  • Paid time off and company holidays
  • Flexible/remote work options
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