At Clario, part of Thermo Fisher Scientific, we develop regulated technology that helps unlock better evidence and improve patient outcomes worldwide. Our software platforms support clinical trials, diagnostics, and medical decision-making in highly controlled regulatory environments.
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.
Competitive compensation
Health, dental, and vision coverage
401(k) retirement plan with company match
Paid time off and company holidays
Flexible/remote work options
Review software specifications and validation documentation to ensure clarity, completeness, and testability.
Manage the full End-to-End (E2E) test cycle process , from initial test design through to final execution and evidence capture.
Design and develop comprehensive test cases , including functional, integration, and performance scenarios.
Execute manual test cases and manage accurate test data for validation activities within regulated environments.
Manage the defect lifecycle utilizing Jira or similar ALM tools, ensuring clear root cause insights and prioritization.
Collaborate with global project teams , specifically coordinating with team members in India; this requires comfort working across international time zones (CST to EST preferred).
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 and risks , providing clear status updates and escalations as needed.
Identify opportunities to improve testing processes, tools, and overall quality practices.
Bachelor’s degree in Information Technology or a related field, or equivalent practical experience.
3+ years in software testing or quality assurance, with a proven track record in End-to-End (E2E) testing
Proficiency with Jira or similar bug-tracking and test management software.
High comfort level collaborating with offshore/global teams (specifically India) and managing the associated communication and scheduling needs.
Proven understanding of the software development lifecycle (SDLC) and validation processes.
Familiarity with documentation systems and a high attention to detail required for regulated environments.
Based in or able to work remotely within the United States (CST or EST time zones preferred).
At Clario, our purpose is to transform lives by unlocking better evidence. It’s a cause that unites and inspires us. It’s why we come to work—and how we empower our people to make a positive impact every day. Whether you're advancing clinical science, building innovative technology, or supporting our global teams, your work helps bring life-changing therapies to patients faster.
Clario is a leading healthcare research and technology company that generates high quality clinical evidence for our pharmaceutical, biotech, and medical device partners. We offer comprehensive evidence generation solutions that combine eCOA, cardiac safety, medical imaging, precision motion, and respiratory endpoints.
Since our founding more than 50 years ago, Clario has delivered deep scientific expertise and broad endpoint technologies to help transform lives around the world. Our endpoint data solutions have supported clinical trials over 26,000 times in more than 100 countries. Our global team of science, technology, and operational experts have supported over 60% of all FDA drug approvals since 2019.
For more information, visit Clario.com
