Oversee the development, support, and enhancement of product lines (e.g., SonoLyst), prototypes, and internal tools.
Provide technical leadership and design authority for the development, evaluation, and deployment of machine learning solutions for ultrasound imaging.
Mentor and support the professional growth of engineers and scientists within the team.
Work within GEHC’s global ISO13485 quality management system to develop medical devices for regulatory submission (e.g., to FDA, CE).
Collaborate with cross-functional teams (console engineering, clinical, regulatory).
Identify and protect intellectual property.
Engage with customers and external partners as needed, both pre- and post-sale.
Contribute to project documentation and process improvement initiatives.
PhD or equivalent experience in a technical discipline (e.g., Computer Science, Engineering, Mathematics).
Significant experience applying machine learning to complex problems in a commercial and ideally regulated setting.
Excellent interpersonal and presentation skills; able to communicate complex concepts to technical and non-technical audiences.
Demonstrated ability to mentor and develop others.
Collaborative, proactive, and able to work independently or as part of a team.
Essential Technical Skills
Strong proficiency in Python and PyTorch for machine learning.
Up-to-date knowledge of modern ML image models (e.g., vision transformers, ConvNeXt, diffusion models such as Stable Diffusion, and foundation models).
Solid understanding of image analysis techniques for noisy data.
Strong coding skills and experience with version control and bug tracking tools.
Experience working within quality management systems and regulated environments.
Experience with cloud-based ML infrastructure (e.g., AWS EKS, Rancher).
Familiarity with ML experiment tracking tools such as Weights & Biases.
Track record of innovation and IP generation.
Experience in agile development environments.
Ideally you will have worked within medical imaging in a regulated environment:
Experience with medical image analysis and DICOM.
Familiarity with regulatory standards (ISO13485, EU AI act).
Knowledge of regulatory pathways for medical devices (FDA, CE).
Experience collaborating with clinical teams.
We would prefer this to be a Cardiff office-based role, but will also consider hybrid working.
GE HealthCare is an Equal Opportunity Employer where inclusion matters. Employment decisions are made without regard to race, color, religion, national or ethnic origin, sex, sexual orientation, gender identity or expression, age, disability, protected veteran status or other characteristics protected by law.
We expect all employees to live and breathe our behaviors: to act with humility and build trust; lead with transparency; deliver with focus, and drive ownership – always with unyielding integrity.
Our total rewards are designed to unlock your ambition by giving you the boost and flexibility you need to turn your ideas into world-changing realities. Our salary and benefits are everything you’d expect from an organization with global strength and scale, and you’ll be surrounded by career opportunities in a culture that fosters care, collaboration, and support.
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Relocation Assistance Provided: No