DEKA Research and Development Corporation

Software Quality Assurance Engineer

Pharmaceuticals & Biotech
5 - 7 years of experience
Job Overview by Ladders

Qualifications

  • Bachelor's degree in Computer Science or related field, advanced degree or certifications a plus.
  • 5-8 years of experience in software quality engineering or development, with 2 years in FDA-regulated sectors.
  • Hands-on programming experience with Go, Java, or Python, and Infrastructure-as-Code tools.
  • Proven ability in creating IEC 62304-compliant documentation for medical software.
  • Practical knowledge of ISO 14971 risk management principles for medical devices.
  • Familiarity with FDA cybersecurity requirements for medical devices, including NIST frameworks.
  • Experience in automated testing using Python, Go, or tools like Playwright.

Responsibilities

  • Embed with engineering teams to standardize documentation practices and automation tools.
  • Author and manage critical software lifecycle documentation artifacts such as SDPs and SRS.
  • Drive change control processes for documentation, coordinating review cycles effectively.
  • Establish and maintain traceability matrices for requirements, designs, and test cases.
  • Manage the documentation project plan in tandem with the engineering release schedule.
  • Facilitate readiness reviews before key engineering milestones and communicate status to teams.

Benefits

  • Opportunity to shape documentation practices within cloud-native engineering teams.
  • Work in a pivotal role without direct management responsibilities.
  • Collaborative environment with access to cutting-edge technologies and frameworks.
Full Job Description
DEKA Research & Development is looking for a technically deep, process-driven Software Quality Assurance Engineer to join our cloud engineering team. This is an individual contributor role with outsized organizational impact: you will work alongside cloud-native engineering teams to learn how they work, codify documentation best practices, and scale those practices across teams building similar products. Additionally, you will champion automation-first, DevSecOps-oriented quality practices to build the documentation and process infrastructure that allows developers to focus on writing great product code - not wrestling with regulatory paperwork. This role does not manage people, it leads through technical credibility, persuasion, and partnership.

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.
To succeed as a Software Quality Assurance Engineer, you will need the following experience and skills:
  • 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
The ideal candidate:
  • 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 Research and Development Corporation

DEKA Research and Development Corporation is a research and development company based in Manchester, New Hampshire. The company was founded in 1982 by Dean Kamen, an inventor and entrepreneur who has over 440 patents to his name. DEKA is known for developing innovative technologies in a variety of fields, including medical devices, robotics, and transportation. Some of the company's most notable inventions include the Segway personal transporter, the iBOT mobility system, and the DEKA Arm prosthetic limb. DEKA has received numerous awards and accolades for its work, including the National Medal of Technology and Innovation in 2000.
Learn more about DEKA Research and Development Corporation
Size
1,000 employees
Industry
Founded
1982

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