Senior Clinical Engineer – RO & GIP

Job Description Summary 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.

Learn more about MIM Software here: https://www.mimsoftware.com/

Job Description 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.

Tr anslate 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 5+ years of molecular imaging Software as a Medical Device experience   OR 7 + 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.

#LI-LRG1 #LI-Onsite #LI-Hybrid #LI-Remote

We will not sponsor individuals for employment visas, now or in the future, for this job opening.

For U.S. based positions only, the pay range for this position is $100,000.00-$150,000.00 Annual. It is not typical for an individual to be hired at or near the top of the pay range and compensation decisions are dependent on the facts and circumstances of each case. The specific compensation offered to a candidate may be influenced by a variety of factors including skills, qualifications, experience and location. In addition, this position may also be eligible to earn performance based incentive compensation, which may include cash bonus(es) and/or long term incentives (LTI). GE HealthCare offers a competitive benefits package, including not but limited to medical, dental, vision, paid time off, a 401(k) plan with employee and company contribution opportunities, life, disability, and accident insurance, and tuition reimbursement.

GE HealthCare offers a great work environment, professional development, challenging careers, and competitive compensation. GE HealthCare is an  Equal Opportunity Employer . 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.

GE HealthCare will only employ those who are legally authorized to work in the United States for this opening. Any offer of employment is conditioned upon the successful completion of a drug screen (as applicable).

While GE HealthCare does not currently require U.S. employees to be vaccinated against COVID-19, some GE HealthCare customers have vaccination mandates that may apply to certain GE HealthCare employees.

Relocation Assistance Provided: Yes

Application Deadline: September 28, 2026