Senior Software QA Engineer

Nova Biomedical:
One Global Brand. One Vision. Together under one name.

Advanced Instruments and Nova Biomedical are now united under one brand, Nova Biomedical, marking a major milestone in our journey to deliver greater value to our customers. By combining our strengths, we're accelerating innovation, supporting critical workflows, and delivering world-class service across the biopharmaceutical and clinical markets.

About The Company

At Nova Biomedical, we’re not just building instruments, we’re powering breakthroughs that improve lives. Our smart, science-driven solutions are trusted in over 100 countries to speed drug development and enhance patient care.

Our integration brings together more than 70 years of scientific excellence with Nova’s cutting-edge innovation, forming a powerhouse of precision, purpose, and possibility. With FDA-registered, ISO-certified manufacturing, more than 125 FDA approvals, and industry-trusted diagnostics, we’re setting new standards in quality and reliability. Nova Biomedical is proud to be a global leader in osmolality testing and biotechnology and in vitro diagnostic (IVD) instrumentation, dedicated to advancing patient care and scientific discovery with a legacy that continues to shape the future of life sciences.

With headquarters in Norwood and Waltham, Massachusetts, and a global team of nearly 2,000 employees, we’re building a collaborative, empowered culture grounded in shared values: Customer Centricity, Ingenuity, Ownership & Accountability, Collaboration, and Integrity.

Working at Nova Biomedical means joining a mission-driven organization where your contributions matter. Whether you're in engineering, science, manufacturing, or support, you’ll be part of a team that values innovation, invests in your growth, and is committed to making a real-world impact on global health.

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About

The Role

The Senior Software QA Engineer will be at the forefront of designing product quality into our next-generation clinical and biopharma Osmometer instruments from the start. Utilizing their experience in modern medical device development, this individual will work closely with our Regulatory Affairs / Quality Assurance and Engineering teams to develop overall test strategy for new products under development. This individual will actively propose and lead process improvements to reduce product development timelines while ensuring the quality and security of our solutions are market leading.

You will be accountable for ensuring proper test case coverage, execution, review, and traceability documentation for assigned projects.

What You’ll Do

• Lead the development, review, and execution of software quality assurance processes and procedures for assigned projects
• Collaborate with cross-functional teams to ensure software development and validation activities meet quality and compliance requirements
• Perform risk assessments and develop mitigation strategies for software-related issues
• Conduct software validation activities in accordance with regulatory standards (FDA, ISO 13485)
• Review and approve software documentation, including validation plans, protocols, and reports
• Participate in internal and external quality audits
• Monitor and analyze software quality metrics to identify trends and areas for improvement
• Provide training and support to team members on software quality and validation processes
• Implement process and tool improvements to bring verification test case writing and approval concurrent with development for iterative development cycles
• Actively participate as a member the development team, including reviewing work item acceptance criteria, providing inputs into work item estimation, and reporting of test status
• Execute manual and automated test cases for verification of requirements and work items within a development iteration

• Proven track record of commercial software test engineering in a medical device, scientific instrument, or similar environment controlling hardware as part of an overall system
• Bachelor's degree or higher in a relevant computer science, engineering subject, or equivalent commercial…