What you will do as a Software Quality Assurance Engineer:
- Embed with engineering teams to understand existing documentation practices and automation tools for software design, V&V activities, and change control, then produce standardized templates, work instructions, and SOPs that can be applied consistently across teams with similar cloud-native product lines.
- Serve as the primary author and owner of software lifecycle documentation artifacts including Software Development Plans (SDPs), Software Requirements Specifications (SRS), Software Design Documents (SDD), Verification & Validation Plans and Reports, and Software Risk Management Files
- Drive document change control processes from initiation through approval, coordinating review cycles to keep releases on schedule.
- Establish and maintain traceability matrices linking software requirements, design elements, risk controls, test cases, and defects, ensuring end-to-end objective evidence is audit-ready at any point in the release cycle.
- Own the documentation project plan for each software release, tracking open documentation tasks, review cycles, and approval gates as a parallel workstream to the engineering release schedule.
- Facilitate documentation readiness reviews prior to design freeze, test execution, and regulatory submission milestones. Communicate readiness status to engineering leads; escalate blockers early and drive resolution.
- Bachelor's degree in Computer Science, Software Engineering, or a closely related technical discipline required.
- Advanced degree or professional certifications (ASQ CSQE, ISTQB, RAC) a plus but not required in lieu of demonstrated experience).
- 5–8 years of combined experience in software quality engineering, software development, or a closely adjacent technical role, with at least 2 years in an FDA-regulated environment (medical devices, digital health, or pharmaceutical software).
- Hands-on software development background — you must be able to read and reason about Go, Java or Python code, Infrastructure-as-Code (Terraform, Ansible), and automated test code (Playwright, pytest) without requiring a developer to walk you through it.
- Demonstrated experience producing IEC 62304-compliant documentation for Class B or Class C software
- Practical knowledge of ISO 14971 risk management methodology as applied to medical device software; experience authoring or materially contributing to FMEAs and software hazard analyses.
- Working knowledge of FDA cybersecurity expectations for medical devices, including familiarity with NIST frameworks and the ability to assess cloud-hosted systems against those standards.
- Familiarity with cloud-native architectures (microservice and event-driven architectures at scale, networking, IAM) sufficient to understand system design documents and workflows.
- Direct experience writing automated tests in Python or Go, or using Playwright for UI/E2E test automation
- You default to automation and repeatability over manual processes, and you can articulate why that matters for regulatory defensibility, not just engineering velocity.
- You are a skilled communicator who can translate between regulatory language and engineering language — equally comfortable in a design review with a Go developer and a regulatory affairs meeting.
- You take documentation quality as seriously as software quality: clarity, precision, version control, and traceability are not overhead to you, they are the work.
- You are comfortable working independently across multiple teams, managing your own priorities, and driving cross-functional coordination without formal authority.
About DEKA:
One hour from the beach, Boston, and the mountains, the historic Amoskeag Millyard once housed the largest textile mills in the world. It is now home to DEKA Research & Development, where we are taking the same innovation and cutting-edge technology into the modern age.
Behind DEKA’s brick walls sits a team of professionals who strive to make a difference every day through thoughtful engineering, design, and manufacturing. Here at DEKA, some of the most innovative and life-changing products of our time are created, and new ideas are always welcome and explored.
Skills Required
- Bachelor's degree in Computer Science, Software Engineering, or closely related technical discipline
- Advanced degree or professional certifications (ASQ CSQE, ISTQB, RAC)
- 5-8 years combined experience in software quality engineering, software development, or closely adjacent technical role
- At least 2 years experience in an FDA-regulated environment (medical devices, digital health, or pharmaceutical software)
- Ability to read and reason about Go, Java, or Python code and automated test code (Playwright, pytest)
- Familiarity with Infrastructure-as-Code (Terraform, Ansible)
- Demonstrated experience producing IEC 62304-compliant documentation for Class B or Class C software
- Practical knowledge of ISO 14971 risk management methodology and experience contributing to FMEAs and software hazard analyses
- Working knowledge of FDA cybersecurity expectations for medical devices, including familiarity with NIST frameworks
- Familiarity with cloud-native architectures (microservices, event-driven architectures, networking, IAM)
- Direct experience writing automated tests in Python or Go or using Playwright for UI/E2E automation
- Automation-first mindset and strong communication to translate between regulatory and engineering stakeholders
What We Do
DEKA is one of the leading research and development companies in the country and is the birthplace of some of the most innovative and life-changing products of our time. For over thirty years, DEKA Research & Development Corp. has made Manchester, New Hampshire home. Located about an hour from Boston, the beach, and the mountains, we are situated in the beautiful and historic Amoskeag Millyard buildings located in downtown Manchester. DEKA continues to be a place where no idea seems too big and where creativity and crazy cool gizmos reign supreme. The engineers, technicians, machinists, designers and all of the other folks who make up DEKA are some of the most creative and innovative professionals you could ever hope to meet. It's a place where one crazy idea can end up being the next greatest invention. At DEKA we embrace the spirit of innovation and constantly aim to turn the impossible into a reality. DEKA is filled with people who are driven to be among the best and brightest in their field of work. It’s a concentrated bunch of really smart thinkers, doers and problems solvers, who are driven to using innovative design solutions and state-of-the-art technology to improve lives. We all see endless possibilities in the power of technology to do good. Employees have the opportunity to work on diverse projects that have a positive, enduring impact on millions of people worldwide. We are growing! We're always seeking passionate individuals to join our growing team of evolved thinkers.








