Software Quality Engineer

GeneDx; United States; On-site; USD 111,000 - 123,000; Full time

Job summary

GeneDx is seeking a Software Quality Engineer, IVD Quality to support software-specific QMS processes, including SDLC, software risk management, and cybersecurity for IVD and digital products. The role reports to the Director, IVD Regulatory and Quality, collaborating with senior IVD Quality team members.

You will act as the Quality representative on software development and bioinformatics teams, guiding and reviewing to ensure documentation and engineering activities meet QMS, regulatory, and

Qualifications

• Bachelor’s or advanced degree in a relevant scientific or technical field (e.g., Computer Science, Engineering, Bioinformatics).
• 6+ years of software QA experience, with 4+ years in medical device or FDA-regulated software development.
• Experience with design controls and regulations: ISO 13485, ISO 14971, IEC 62304.
• Experience with software as a Medical Device and regulatory submissions/audits.
• Ability to manage multiple projects in a fast-paced environment.

Responsibilities

• Execute assigned software-development Quality activities and support the build-out of SDLC QMS processes.
• Provide Quality reviews and process oversight for software design-control activities (requirements, architecture, code-review, V&V) for compliance and audit readiness.
• Develop and review Design and Development File documentation across the product lifecycle.
• Serve as Quality representative for software risk-management throughout the lifecycle.
• Provide Quality support for validation of non-product software tools used in operations, product testing, and the quality system.
• Support investigations and resolutions of software-related nonconformances, deviations, and CAPAs.
• Provide Quality input on cybersecurity design-control, risk-management, vulnerability-management, and post-market activities per FDA guidance.

Skills

Software QA experience

Regulatory knowledge

Multitask management

Remote work discipline

Education

Bachelor's or higher in CS/Engineering/Bioinformatics

CSQE certification preferred

Job description

• The Software Quality Engineer, IVD Quality supports the development, implementation, and maintenance of software-specific QMS processes, including Software Development Life Cycle (SDLC), Software Risk Management, and Cybersecurity, for GeneDx’s IVD and digital products. The role reports to the Director, IVD Regulatory and Quality and works in close partnership with senior members of the IVD Quality team.
• Serving as the Quality representative on software development and bioinformatics teams, the Software Quality Engineer provides Quality review, guidance, and process support to ensure that software engineering activities and supporting technical documentation meet established QMS, regulatory, and standards requirements (e.g., IEC 62304 and ISO 62366).

Summary

• The Software Quality Engineer, IVD Quality supports the development, implementation, and maintenance of software-specific QMS processes, including Software Development Life Cycle (SDLC), Software Risk Management, and Cybersecurity, for GeneDx’s IVD and digital products. The role reports to the Director, IVD Regulatory and Quality and works in close partnership with senior members of the IVD Quality team.
• Serving as the Quality representative on software development and bioinformatics teams, the Software Quality Engineer provides Quality review, guidance, and process support to ensure that software engineering activities and supporting technical documentation meet established QMS, regulatory, and standards requirements (e.g., IEC 62304 and ISO 62366).

Job Responsibilities

• Execute assigned software-development Quality activities and support the build-out of associated SDLC QMS processes.
• Provide Quality review and process oversight for software design-control activities, including software requirements, architecture documentation, code-review records, and verification and validation documentation, to support compliance and audit readiness.
• Participate in the development and review of Design and Development File documentation throughout the product lifecycle.
• Serve as the Quality representative for software risk-management activities, providing guidance and review throughout the software lifecycle.
• Provide Quality support for validation of non-product software tools used in operations, product testing, and the quality system.
• Support the investigation and resolution of software-related nonconformances, deviations, and CAPAs.
• Provide Quality input on cybersecurity-related design-control, risk-management, vulnerability-management, and post-market activities to support alignment with applicable FDA cybersecurity guidance and established QMS requirements.
• Support internal and external audits by preparing software-related objective evidence and assisting with responses to findings.
• Monitor evolving regulatory expectations, standards, and best practices for software in IVDs, including FDA and international guidance; recommend updates to applicable processes and documentation.
• Contribute to continuous improvement initiatives related to software development and quality processes.

Education, Experience, And Skills

• A bachelor’s or advanced degree in a relevant scientific or technical field (e.g., Computer Science, Engineering, Bioinformatics).
• 6+ years of software QA experience, with 4+ years in medical device or FDA-regulated software development.
• Practical experience with design controls, ISO 13485, ISO 14971, IEC 62304 regulations.
• Experience with Software as a Medical Device or medical devices containing software. Strong understanding of design control procedures and the software development lifecycle in regulated environments.
• Experience supporting regulatory submissions and audits.
• Ability to manage multiple projects and priorities in a fast-paced environment.

Certificates, Licenses, Registrations

• Certified Software Quality Engineer (CSQE) preferred.

Work Environment

• This is a fully remote position. The employee will work from a home office or other suitable remote location with reliable high-speed internet access. Work is performed in a climate-controlled environment using standard office equipment including computer, phone, and video conferencing tools. Your standard work schedule and hours will be established in collaboration with your leader and may be adjusted to align with evolving business needs.
• Standard work hours are Monday through Friday, 9 AM to 5 PM EST.

Pay Transparency, Budgeted Range

$111,249—$122,620 USD

A culture that plays to win, because patients are counting on us. At GeneDx, we’re driven by urgency and purpose: helping patients get diagnosed earlier. Our mission, to empower everyone to live their healthiest life through genomics, drives our team to make a tangible impact each day – and shapes our culture where high standards, strong teamwork, and meaningful ownership are the norm. We act with intention, support one another, and deliver work we’re proud to put our names on.

Here’s what you can expect day to day:

• Play like a champion (step up, redefine what’s possible, own it)

We bring energy, focus, and a bias for action. We step up, take initiative, and deliver on our commitments – with quality, speed, and care.

• Think bigger (stretch beyond, courage not consensus)

We push past the obvious. We challenge assumptions, raise the bar, and make thoughtful, decisive calls — choosing progress over perfection.

• Grow fast (be curious, speak up, be agile)

We stay curious, ask questions, and share direct feedback with respect. We adapt quickly and keep learning through collaboration and continuous improvement.

If you’re motivated by meaningful work, a fast-moving environment, and teammates who care deeply about outcomes, you’ll thrive at GeneDx.

At GeneDx, we believe in taking care of our people. We provide competitive compensation and benefits that reflect local market practices and legal requirements in each country where we operate, helping employees thrive both professionally and personally.

We welcome everyone regardless of their background. All qualified applicants will receive consideration for employment without regard to race, color, religion, national origin, sex, gender, gender identity, sexual orientation, protected veteran status, disability, age, and other characteristics protected by law.

GeneDx is a place where people from all backgrounds can make an impact.

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