Senior Clinical Engineer RO & GIP

Senior Clinical Engineer RO & GIP

Help advance more precise, personalized care This role sits within GE HealthCare's MIM Software business, where we build vendor-neutral imaging software designed to simplify complex clinical workflows and support better decision-making in patient care. Leading healthcare organizations around the world use MIM to help deliver more precise, personalized care to patients. If you're excited about combining clinical insight, technology, and cross-functional collaboration to improve healthcare outcomes, this could be a meaningful next step in your career.

About the role

As a Senior Clinical Engineer RO & GIP, you will help guide the clinical development of imaging products, diagnostics, and Software as a Medical Device (SaMD). You'll play an important role in evaluating safety, effectiveness, and clinical value, while helping translate clinical and customer needs into product direction and innovation. This role aligns with our Radiation Oncology and Guided Intervention Platform product lines.

This position has a strong execution focus and offers the opportunity to contribute meaningfully within established practices and procedures, while also applying sound judgment, analytical thinking, and collaboration to solve problems and move work forward. You'll work closely with multidisciplinary partners across engineering, regulatory, quality, marketing, and clinical settings, with opportunities to deepen your expertise and grow your impact over time.

Important work authorization note: Legal authorization to work in the U.S. is required. We are unable to sponsor employment visas now or in the future for this position.

What you'll do

Support the clinical development of imaging products, diagnostics, and Software as a Medical Device by helping determine safety, effectiveness, and clinical value.

Translate clinical and customer needs into functional requirements that inform product development.

Contribute to software prototyping, support verification and validation (V&V) testing, and help drive iterative improvements following product launch.

Lead and contribute to cross-functional initiatives that support product success, including work related to:

• Product roadmap execution and product lifecycle planning
• Software as a Medical Device regulatory submissions (such as 510(k))
• Sponsored research agreements

Build and maintain technical and clinical expertise within your area through activities such as:

• Reviewing scientific literature
• Conducting customer interviews
• Attending conferences
• Visiting clinical sites

Apply an understanding of business priorities to help execute strategy and deliver results that support broader organizational goals.

Use judgment, prior experience, analytical thinking, and guidance from others to recommend practical solutions, including those that may extend beyond standard approaches.

Collaborate closely with internal partners across engineering, regulatory, quality, and marketing, as well as with external clinical professionals.

Contribute as a strong individual team member and, where applicable, provide informal mentorship, guidance, and knowledge-sharing to more junior colleagues.

Required qualifications

• Bachelor's degree from an accredited college or university in a relevant field such as:
• Biomedical Engineering
• Radiologic Technology or Radiologic Sciences
• Computer Science
• Medical Physics
• Or a related discipline
• 3 + years of molecular imaging Software as a Medical Device experience OR 5 + years of closely related adjacent experience
• Strong problem-solving and analytical skills
• Ability to communicate and collaborate effectively with:
• Clinical professionals
• Engineering, regulatory, quality, and other cross-functional internal teams
• Demonstrated ability and aptitude to build clinical, anatomical, and technical domain knowledge
• Willingness to travel periodically for medical conferences, customer meetings, and site visits
• Legal authorization to work in the U.S. without current or future visa sponsorship

Preferred qualifications

• Master's degree or PhD in a relevant field
• Prior experience in the software or medical device industry; strong familiarity with design controls and regulatory submissions
• Direct experience with imaging software
• Strong technical writing skills
• Strong communication skills, including the ability to:
• Tailor messages for both technical and non-technical audiences
• Explain complex concepts clearly and concisely
• Communicate progress and risks effectively to non-technical stakeholders
• Experience working successfully in team-based environments
• Project management skills, including planning, documentation, and execution
• Experience mentoring junior engineers, delegating appropriately, and supporting team growth
• Recognized depth of expertise in advanced molecular imaging software

What will help you succeed in this role

• A proactive, growth-oriented mindset
• Curiosity and a thoughtful approach to investigating complex problems
• The ability to analyze challenges and develop effective solutions
• Strong written, verbal, and technical communication skills
• A collaborative working style and commitment to shared outcomes
• Interest in continuous learning and deepening your clinical and technical expertise

Why this role matters

This is an opportunity to help shape products that support clinicians and improve the patient experience. Your work will contribute to technologies used in complex clinical scenarios, and your voice will help influence how products evolve over time. You'll join a collaborative environment where clinical insight, technical innovation, and cross-functional partnership all play an important role in delivering meaningful healthcare impact.