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Über
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.
Explore what's next with us
at novabiomedical.com or aicompanies.com
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 What we are looking for in you
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 software engineering experience Commercial experience testing and shipping medical devices under ISO 13485 Familiarity with current FDA requirements and guidance for cybersecurity Familiarity with feature, regression, and integration testing Experience utilizing Azure DevOps or similar systems for backlog, sprint boards, and test case management Understanding and practice of working in, and testing solutions for, regulatory compliant environments Skills in Setup and configuration of PC, server, cloud hosted, and hardware test environments Understanding and experience with both business-oriented Agile and waterfall software development lifecycles Knowledge with 21 CFR Part 11 requirements Experience testing devices to published 3rd party communication protocols and APIs Physical Requirements for this role include:
The full list of physical requirements for this role is available upon request. Standard office environment Why work for Nova Biomedical
Flexible Medical, Dental, & Vision Coverage Competitive 401k company match Bonus Program, Generous PTO and paid holidays Generous Tuition reimbursement Hybrid and flexible work arrangements Professional development, engagement and events Company marketplace for lunch and snacks in our Norwood, MA, Billerica, MA and Westbrook, ME offices Company subsidized cafeteria in our Waltham, MA office
Work Location:
Hybrid work schedule on-site in
Norwood , 4 days/week on-site
Targeted Salary Range: $130,000- $170,000/year
Nova Biomedical believes in transparency and integrity throughout all we do, including compensation. The provided salary range for this role represents the expected base salary or hourly rate for this opening. Actual compensation will be commensurate with the candidate's experience and may vary based on individual factors such as location, skills, and education.
EEO Statement:
Nova Biomedical takes pride in being an equal opportunity employer committed to hiring a diverse and inclusive workforce. As a part of our commitment to a diverse and inclusive workforce, Nova Biomedical will continue to take steps to assure that recruitment, hiring, assignment, promotion, compensation, and all other personnel decisions are made and administered without regard to race, religion, color, national origin, citizenship, sex, sexual orientation, gender identity, gender expression, veteran status, age, mental or physical disability, genetic information or any other protected class.
Privacy policy
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Sprachkenntnisse
- English
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