Senior Software V&V Engineer

Natera; United States; Hybrid; USD 140,000 - 190,000; Full time

Job summary

Natera, a leader in cfDNA testing, invites a Senior Software V&V Engineer to own verification and validation across regulated medical device software and NGS pipelines. You’ll work with bioinformaticians, software engineers, and clinical labs to ensure compliant, audit-ready documentation and traceability.

This role requires deep regulatory fluency (IEC 62304, ISO 13485), strong testing design skills, and collaboration across functions. Travel to Boulder, CO is expected.

Qualifications

• 4+ years conducting and overseeing software verification and validation for regulated medical device software (510(k) and/or PMA).
• 3+ years designing and executing verification tests for NGS bioinformatics pipelines and algorithms.
• 2+ years testing experience in cloud environments (AWS or GCP).
• Direct working knowledge of ISO 13485 and IEC 62304 design controls—applied experience.
• Cross-functional collaboration with bioinformaticians, software engineers, and clinical laboratories.

Responsibilities

• Own verification and validation activities across regulated software portfolios with QA, bioinformatics, and clinical teams.
• Align testing processes with IEC 62304 and ISO 13485 design controls and ensure audit-ready documentation.
• Design and execute verification tests for NGS bioinformatics pipelines and algorithms.
• Develop and maintain IEC 62304-aligned test templates, protocols, and test cases.
• Review executed test cases, assess variances, and document findings with QA.
• Establish and maintain V&V traceability across device software, lab tools, and instruments.
• Manage cadence, prioritization, and execution of V&V activities across programs.
• Travel to the Boulder, CO lab regularly to support testing activities.

Skills

V&V engineering

Regulatory testing

NGS bioinformatics

Cloud testing

Cross-functional collaboration

Regulatory documentation

Communication skills

Job description

When a clinician receives an MRD result from our platform, every line of software that touches that result needs to have been verified and validated to the highest standard. At Foresight Diagnostics — now part of Natera — that responsibility belongs to our V&V team. We're looking for a Senior Software V&V Engineer who understands bioinformatics pipelines deeply enough to test them rigorously, and who brings the regulatory fluency to ensure every test case, protocol, and traceability matrix holds up under scrutiny.

ABOUT FORESIGHT DIAGNOSTICS

Foresight Diagnostics is a molecular diagnostics company pioneering non-invasive cancer detection through highly sensitive, cell-free DNA-based liquid biopsy technologies. Our proprietary methods - originally developed at Stanford University - are designed to detect smaller tumors earlier and enable more personalized treatment strategies for patients with cancer.

We sit at the intersection of molecular biology, bioinformatics, and next-generation sequencing (NGS), and we translate rigorous science into clinically meaningful solutions. Following our acquisition by Natera, we now combine the agility of a mission-driven startup with the scale and resources of a global leader in cell-free DNA testing. It’s an exciting moment to join us.

Headquartered in Boulder, Colorado, our team operates in a high accountability, collaborative environment where quality and continuous improvement aren’t just values - they’re how we work every day.

WHY THIS ROLE EXISTS

Our software portfolio spans bioinformatics pipelines, reagent QC systems, liquid handling automation, LIMS/LIS integrations, and NGS analysis tools. Each component carries regulatory obligations under IEC 62304 and ISO 13485, and each needs to be verified and validated with the rigor that clinical diagnostics demands.

WHAT YOU’LL DO

You'll own verification and validation activities across Foresight's software portfolio — working closely with bioinformaticians, software engineers, and clinical laboratory teams to ensure every system is tested thoroughly and documented completely.

In practice, that means:

• Aligning all software testing processes with IEC 62304 and ISO 13485 design control requirements, and ensuring the team operates consistently within that framework.
• Overseeing V&V activities for pipeline software, lab automation methods, reagent QC software, LIMS/LIS tools, and select laboratory instruments.
• Designing and executing software verification tests for NGS bioinformatics pipelines — including tests for end-to-end analysis workflows and individual NGS algorithms.
• Developing and maintaining test templates, test protocols, and IEC 62304-aligned test cases that are clear, complete, and audit-ready.
• Reviewing executed test cases, assessing variances, and collaborating with the Quality Assurance team to resolve and document findings appropriately.
• Approving test reports and ensuring full documentation compliance under design controls.
• Establishing and maintaining V&V traceability across device software, lab automation tools, and lab instruments — including oversight of software traceability matrices across all device software components.
• Managing the cadence, prioritization, and execution of V&V activities across concurrent programs.
• Traveling to the Foresight lab in Boulder, CO on a regular basis to support testing activities, lab integration work, and cross-functional collaboration.

WHAT YOU’LL BRING

Required

• 4+ years conducting and overseeing software verification and validation activities for regulated medical device software (510(k) and/or PMA pathways).
• 3+ years designing and executing verification tests specifically for NGS bioinformatics pipelines — including NGS analysis workflows and individual algorithm testing.
• 2+ years of testing experience in cloud environments (AWS or GCP).
• Direct working knowledge of ISO 13485 and IEC 62304 design controls — applied experience, not just familiarity.
• Prior experience working cross-functionally with bioinformaticians, software engineers, and clinical laboratory teams.
• Prior work experience in bioinformatics, computational biology, or a biology-related field — this is a hard requirement for this role.
• Excellent written and verbal communication skills, with the ability to translate complex technical findings into clear, compliant documentation.

Preferred

• Testing experience with pipeline orchestration tools such as Nextflow.
• Hands-on exposure to clinical laboratory workflows — CAP/CLIA environment experience is a meaningful advantage.
• Familiarity with LIMS/LIS platforms in a regulated diagnostic context.
• Experience contributing to or preparing for FDA submissions (510(k) or PMA) from a V&V documentation standpoint.

WHY JOIN US

This is a technically sophisticated role at the intersection of bioinformatics and regulated software quality — a combination that's genuinely rare and increasingly in demand as molecular diagnostics scales. You'll work on software systems that directly enable MRD detection for cancer patients, alongside scientists and engineers who take both the science and the standards seriously.

With Natera's backing and Foresight's mission, you'll have the resources of an established organization and the ownership opportunities of a focused, growing team. We invest in our people and promote from within for those who deliver.

LOCATION & TRAVEL

This role offers location flexibility with regular required travel to our Boulder, Colorado laboratory. Travel frequency will be discussed during the interview process and will vary based on program needs, audit schedules, and lab integration milestones. Candidates should be comfortable with periodic in-person presence as a genuine part of the role.

OUR OPPORTUNITY

Natera™ is a global leader in cell-free DNA (cfDNA) testing, dedicated to oncology, women’s health, and organ health. Our aim is to make personalized genetic testing and diagnostics part of the standard of care to protect health and enable earlier and more targeted interventions that lead to longer, healthier lives.

The Natera team consists of highly dedicated statisticians, geneticists, doctors, laboratory scientists, business professionals, software engineers and many other professionals from world‑class institutions, who care deeply for our work and each other. When you join Natera, you’ll work hard and grow quickly. Working alongside the elite of the industry, you’ll be stretched and challenged, and take pride in being part of a company that is changing the landscape of genetic disease management.

WHAT WE OFFER

Competitive Benefits - Employee benefits include comprehensive medical, dental, vision, life and disability plans for eligible employees and their dependents. Additionally, Natera employees and their immediate families receive free testing in addition to fertility care benefits. Other benefits include pregnancy and baby bonding leave, 401k benefits, commuter benefits and much more. We also offer a generous employee referral program!

Natera is proud to be an Equal Opportunity Employer. We are committed to ensuring a diverse and inclusive workplace environment, and welcome people of different backgrounds, experiences, abilities and perspectives. Inclusive collaboration benefits our employees, our community and our patients, and is critical to our mission of changing the management of disease worldwide.

All qualified applicants are encouraged to apply, and will be considered without regard to race, color, religion, gender, gender identity or expression, sexual orientation, national origin, genetics, age, veteran status, disability or any other legally protected status. We also consider qualified applicants regardless of criminal histories, consistent with applicable laws.

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