Software Quality Engineer (V&V)

Reposted 8 Days Ago
Hiring Remotely in United States
Remote
Junior
Healthtech • Software
The Role
Validate clinical study software to ensure quality and compliance by designing test cases, executing tests, analyzing results, and collaborating with teams to improve software reliability.
Summary Generated by Built In

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.

What We Offer
  • Competitive compensation

  • Health, dental, and vision coverage

  • 401(k) retirement plan with company match

  • Paid time off and company holidays

  • Flexible/remote work options

What You’ll Be Doing
  • 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.

What We Look For
  • 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.

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The Company
HQ: Philadelphia, PA
6,733 Employees
Year Founded: 1972

What We Do

-- Clario has been named a Top Workplace by Energage for the 2022 Top Workplaces USA national awards. -- Clario generates the richest clinical evidence by fusing our deep scientific expertise and global scale into the broadest endpoint technology platform. By doing this, we empower our partners to transform lives. With almost 50 years of experience, 19,000 clinical trials, and 870 regulatory approvals, Clario has mastered the ability to generate rich evidence across a Trial Anywhere™ portfolio: decentralized (DCT), hybrid and site-based clinical trials. With 30 facilities in nine countries across North America, Europe, and Asia Pacific, Clario delivers the power of certainty. Partners ————— Clario brings the best of ERT and Bioclinica together to work alongside our partners to solve some of their biggest questions on topics such as: - eCOA vs. paper - Decentralized Clinical Trial (DCT) - Rescue a clinical trial - Broad endpoint technology: cardiac safety, imaging, respiratory And many more. People ———— We are so honoured to be named a 2022 Top Workplace by Energage. One of our leading values at Clario is People First Always. We help individuals build meaningful careers at Clario as they serve to help transform patients lives. Join us on this journey and check out our careers page: https://clario.com/careers/

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