Software Quality Engineer II (V&V)

Clario; Bengaluru; Hybrid; INR 800,000 - 1,200,000; Full time

Benefits offered by this job

Competitive pay and incentives

Provident fund and medical insurance

Engaging employee programs

Remote work flexibility

Job summary

Clario, a part of Thermo Fisher Scientific, is a global leader in endpoint technology solutions for clinical trials. We are hiring a Software Quality Engineer (V&V) to support verification and validation activities for enterprise-level clinical software products in a fast-paced Agile setting.

This hybrid role requires regular onsite collaboration with the Software Quality Engineering team in Bangalore. We offer competitive pay, provident fund, medical insurance, engaging employee programs,

Qualifications

• 3-5 years of experience in enterprise software testing or quality assurance.
• Strong understanding of the Software Testing Life Cycle (STLC).
• Experience with manual and automated testing tools.
• Basic ability to write SQL select queries.
• Familiarity with web-based applications and system workflows.

Responsibilities

• Participate in software testing activities including test review, test execution, and test witnessing within an Agile development lifecycle.
• Review PRDs, Engineering Functional Specifications, and test plans to support accurate test scoping and planning.
• Execute test cases, document results, and ensure timely reporting of defects and issues.
• Collaborate with software engineers to investigate, troubleshoot, and resolve defects identified during testing.
• Diagnose failures across environments with QA team members, developers, and DBAs.

Skills

STLC knowledge

Manual testing

Analytical skills

Communication

Problem solving

Education

B.E. in Biomedical Engineering / Electronics / Computer Science or related field

Tools

SQL

Manual & Automated testing tools

Job description

Clario, a part of Thermo Fisher Scientific, is a global leader in endpoint technology solutions for clinical trials. We are seeking a Software Quality Engineer (V&V) to support verification and validation activities for enterprise-level clinical software products. This role is ideal for professionals with prior experience in software testing who are looking to deepen their expertise in quality engineering, contribute to high-impact clinical systems, and operate within a fast-paced Agile environment. This is a hybrid role requiring regular onsite collaboration with the Software Quality Engineering team in Bangalore.

What We Offer

• Competitive pay and incentives
• Provident fund and medical insurance
• Engaging employee programs and local events
• Modern office spaces and remote work flexibility

What You’ll Be Doing

• Participate in software testing activities including test review, test execution, and test witnessing within an Agile development lifecycle
• Review Product Requirement Documents (PRDs), Engineering Functional Specifications, and test plans to support accurate test scoping and planning
• Execute test cases, document results, and ensure timely and accurate reporting of defects and issues
• Collaborate with software engineers to investigate, troubleshoot, and resolve defects identified during testing
• Work with QA team members, developers, and system/database administrators to diagnose failures across multiple environments
• Analyze requirements to identify gaps, edge cases, and risk areas, contributing to improved product quality
• Support test planning activities by identifying dependencies, risks, and required test coverage
• Follow established QA processes, standards, and regulatory requirements to ensure compliance and consistency
• Troubleshoot application issues and support root cause analysis efforts
• Contribute to documentation, quality records, and audit readiness activities
• Read, understand, and make small modifications to scripts (e.g., Python, JavaScript) to support testing activities
• Leverage basic scripting or automation techniques to improve efficiency in repetitive testing or validation tasks
• Manage competing priorities effectively in a dynamic project environment and elevate risks appropriately
• Mentoring New joiners

What We Look For

• Bachelor of Engineering in Biomedical Engineering, Electronics, Computer Science, or a related field
• 3 -5 years of experience in enterprise software testing or quality assurance
• Strong understanding of the Software Testing Life Cycle (STLC)
• Experience with manual testing concepts including test cases, scenarios, and defect life cycle
• Familiarity with manual and automated testing tools
• Basic understanding of databases with ability to write SQL select queries
• Familiarity with web-based applications and system workflows
• Strong analytical and problem-solving skills
• Ability to work independently and collaboratively in a team environment
• Strong communication and documentation skills
• Ability to adapt to changing priorities in a fast-paced environment
• Exposure to cloud technologies, DevOps practices, or Amazon Cloud automation is a plus

Location

Hybrid role – working from our Bangalore office 3–4 days per week

At Clario, part of Thermo Fisher Scientific, 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 Privacy Policy Clario is a leading provider of endpoint data solutions to the clinical trials industry, generating high-quality clinical evidence for life sciences companies. We offer comprehensive evidence generation solutions that combine medical imaging, eCOA, precision motion, cardiac solutions and respiratory endpoints. For more than 50 years, Clario has delivered deep scientific expertise and broad endpoint technologies to help transform lives around the world. Our endpoint data solutions have supported over 30,000 clinical trials in more than 100 countries. Our global team of science, technology, and operational experts have supported over 70% of all FDA drug approvals since 2015.