Principal AI Quality Engineer

Posted 19 Days Ago
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Vista, CA, USA
In-Office
160K-180K Annually
Senior level
Biotech
The Role
The Principal AI Quality Engineer oversees QA for AI-driven medical software, ensuring compliance and leading quality activities, mentoring junior staff, and collaborating across teams. The role requires expertise in AI/ML, regulatory standards, and project management.
Summary Generated by Built In

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 AIdriven medical device software, overseeing endtoend 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 crossfunctional 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 crossfunctional 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 presubs, 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 rootcause 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 AIfocused 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.

#LI-LCS

Join our winning team today. Together, we’ll accelerate the real-life impact of tomorrow’s science and technology. We partner with customers across the globe to help them solve their most complex challenges, architecting solutions that bring the power of science to life.

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 [email protected].

Skills Required

  • Bachelor's or master's degree in computer science, Data Science, Artificial Intelligence or a related technical field
  • 5+ years of quality experience in medical devices, IVD, or similarly regulated industries
  • Deep expertise in AI/ML algorithms, model validation, and regulated software development
  • Strong knowledge of regulatory standards for AI/ML and SaMD
  • Proven ability to lead AI-focused risk management processes
  • Demonstrated leadership, project management, and communication skills

Cepheid Compensation & Benefits Highlights

The following summarizes recurring compensation and benefits themes identified from responses generated by popular LLMs to common candidate questions about Cepheid and has not been reviewed or approved by Cepheid.

  • Leave & Time Off Breadth PTO and paid holidays are portrayed as robust, with formal programs and mentions of generous time off and rollover in some cases. This breadth supports a positive view of time-off availability.
  • Healthcare Strength Core medical, dental, and vision coverage is highlighted repeatedly and is viewed as comprehensive for regular full‑time employees. Descriptions such as “good” or “great” benefits reinforce the strength of the health coverage.
  • Retirement Support A 401(k) plan with company matching is consistently included as part of the package. The presence of matching contributions strengthens perceived retirement readiness.

Cepheid Insights

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The Company
HQ: Sunnyvale, CA
4,883 Employees
Year Founded: 1996

What We Do

Cepheid is dedicated to improving healthcare by pioneering molecular diagnostics that combine speed, accuracy, and flexibility. The company's GeneXpert® systems and Xpert® tests automate highly complex and time-consuming manual procedures, providing A Better Way for institutions of any size to perform world-class PCR testing. Cepheid’s broad test portfolio spans respiratory infections, blood virology, women’s and sexual health, TB and emerging infectious diseases, healthcare-associated infectious diseases, oncology and human genetics. The company’s solutions deliver actionable results where they are needed most – from central laboratories and hospitals to near-patient settings. For more information, visit http://www.cepheid.com.

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