Principal AI Quality Engineer

Danaher Corporation; Vista (CA); On-site; USD 160,000 - 180,000; Full time

Benefits offered by this job

Benefits package

Job summary

Leica Biosystems, a Danaher operating company, is seeking an AI Quality Engineer to lead QA efforts for AI/ML medical device software, ensuring safety, regulatory alignment and product quality. This on-site role reports to the Director of QA and Regulatory Compliance in Vista, CA.

You will partner with R&D, regulatory, and clinical teams, mentor junior engineers, and drive risk management and V&V activities across the AI/ML lifecycle to uphold rigorous standards and continuous improvement.

Qualifications

• Experience with AI/ML algorithms, model validation and regulated software/dev.
• Proven ability to lead AI-focused risk management and quality processes.
• Strong leadership, project management and communication skills across AI/ML, Digital Health, Cybersecurity.

Responsibilities

• Represent the Quality Engineering function on cross-functional teams, contributing to design controls and DHF development.
• Lead AI/ML quality assurance strategies aligned with FDA, MDR, IVDR and ISO standards.
• Partner with data scientists, software engineers and clinical experts to meet regulatory and performance expectations.
• Support regulatory submissions such as FDA pre-sub, 510(k) and IVDR CE while driving AI/ML risk management.
• Lead lifecycle quality activities including V&V, CAPA, audits, and mentoring junior engineers.

Skills

AI/ML expertise

Regulatory knowledge

Leadership

Cross-functional collaboration

Education

Bachelor’s or Master’s in CS/DS/AI

Job description

Bring more to life.

Are you ready to accelerate your potential and make a real difference within life sciences, diagnostics and biotechnology?

At Leica Biosystems, one of Danaher’s 15+ operating companies, our work saves lives—and we’re all united by a shared commitment to innovate for tangible impact.

You’ll thrive in a culture of belonging where you and your unique viewpoint matter. And by harnessing Danaher’s system of continuous improvement, you help turn ideas into impact – innovating at the speed of life.

At Leica Biosystems, we’re not just shaping the future of cancer diagnostics — we’re transforming lives. Our mission of “Advancing Cancer Diagnostics, Improving Lives” is the driving force behind everything we do. As a global leader with the most comprehensive portfolio spanning from biopsy to diagnosis, we empower clinicians with innovative, reliable solutions so they can give patients timely, accurate answers when they need them most. When you join Leica Biosystems, you’re not just taking a job; you’re becoming part of a passionate team that knows every moment matters when it comes to cancer. You’ll help develop diagnostic solutions that turn anxiety into answers, and aid the acceleration of next‑generation, life‑changing therapies. Surrounded by a diverse and collaborative global community, you’ll be inspired each day to stretch, grow, and make an impact.

Learn about the Danaher Business System which makes everything possible.

The AI Quality Engineer leads quality assurance efforts for AI ‑ driven medical device software, overseeing end ‑ to ‑ end lifecycle development and compliance activities for Artificial intelligence (AI)/machine learning (ML) models to ensure safety, effectiveness, and regulatory alignment. This role partners closely with R&D, clinical, regulatory, and product teams to guide AI/ML solutions through rigorous quality and compliance processes. The engineer also mentors junior team members, strengthens cross ‑ functional collaboration, and upholds the highest standards of product quality throughout the organization.

This position reports to the Director, Quality Assurance and Regulatory Compliance and is part of the Quality team located in Vista, CA and will be an on‑site role.

In this role, you will have the opportunity to:

• Represent the Quality Engineering function on cross ‑ functional teams, contributing to design controls, process controls, verification/validation activities, and Design History File development.
• Lead the development and execution of AI/ML quality assurance strategies aligned with global regulations and standards, including FDA, MDR, IVDR, IEC 5338, IEC 23053, EC 8183, IEEE 2801, ISO 13485, and IEC 62304.
• Partner with data scientists, software engineers, and clinical experts to ensure AI/ML solutions meet clinical, regulatory, and performance expectations.
• Support global regulatory submissions, such as FDA pre ‑ subs, 510(k), and IVDR CE, while driving AI/ML risk management, including hazard analysis, mitigation planning, and evaluation of model robustness, bias, and fairness.
• Lead AI/ML lifecycle quality activities, including V&V best practices, CAPA and root ‑ cause investigations, audit/inspection readiness, and mentoring of junior engineers while staying current on evolving regulatory and industry trends.

The essential requirements of the job include:

• Bachelor’s or master’s degree in computer science, Data Science, Artificial Intelligence or a related technical field; advanced degree preferred, with 5+ years of quality experience in medical devices, IVD, or similarly regulated industries.
• Deep expertise in AI/ML algorithms, model validation, evaluation techniques, and regulated software or embedded software development.
• Strong knowledge of regulatory standards for AI/ML and SaMD, including FDA 21 CFR Part 820, IEC 5338, ISO 13485, IEC 62304, and FDA AI/ML guidance.
• Proven ability to lead AI ‑ focused risk management processes, supported by strong analytical skills and a commitment to patient safety and product quality.
• Demonstrated leadership, project management, and communication skills, with experience across AI/ML, Digital Health, Cybersecurity, and Interoperability.

It would be a plus if you also possess previous experience in:

• Familiarity with Good Machine Learning Practices (GMLP) and FDA’s AI/ML regulatory framework.
• Experience with post-market surveillance and monitoring of AI/ML models.
• Knowledge of digital health, cybersecurity, interoperability, and cloud‑based SaMD deployment considerations.
• Effective presentation and communication skills, with ability to engage both technical and non‑technical stakeholders.
• Strong organizational and project management skills to meet regulatory and product development timelines
• Possible international

Leica Biosystems, a Danaher operating company, offers a broad array of comprehensive, competitive benefit programs that add value to our lives. Whether it’s a health care program or paid time off, our programs contribute to life beyond the job. Check out our benefits at Danaher Benefits Info.

The annual salary range for this role is $160,000 - $180,000. This is the range that we in good faith believe is the range of possible compensation for this role at the time of this posting. This range may be modified in the future.

This job is also eligible for bonus/incentive pay.

We offer comprehensive package of benefits including paid time off, medical/dental/vision insurance and 401(k) to eligible employees.

Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company’s sole discretion unless and until paid and may be modified at the Company’s sole discretion, consistent with the law.

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For more information, visit www.danaher.com.

Danaher Corporation and all Danaher Companies are committed to equal opportunity regardless of race, color, national origin, religion, sex, age, marital status, disability, veteran status, sexual orientation, gender identity, or other characteristics protected by law.

The U.S. EEO posters are available here.

We comply with federal and state disability laws and make reasonable accommodations for applicants and employees with disabilities. If reasonable accommodation is needed to participate in the job application or interview process, to perform essential job functions, and/or to receive other benefits and privileges of employment, please contact:1-202-419-7762 or [e-mail].