GE HealthCare
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 aSenior Clinical Engineer – RO & GIP, you will help guide the clinical development of imaging products, diagnostics, andSoftware as a Medical Device (SaMD).You’llplayan important rolein 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 GuidedIntervention 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’llwork closely with multidisciplinary partners across engineering, regulatory, quality, marketing, and clinical settings, with opportunities to deepen yourexpertiseand grow your impact over time.
Important work authorization note:
Legal authorization to work in the U.S. isrequired.We are unable to sponsor employment visas now or in the future for this position.
Whatyou’lldo
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Support the clinical development of imaging products,diagnostics, and Software as a Medical Device by helpingdeterminesafety, effectiveness, and clinical value.
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Translate clinical and customer needs into functional requirements that inform product development.
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Contribute tosoftware prototyping, supportverificationand validation (V&V) testing, and help drive iterative improvements following product launch.
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Lead and contribute to cross-functional initiatives that support product success, including work related to:
- Product roadmapexecutionandproductlifecycle planning
- Software as a Medical Device regulatory submissions (such as 510(k))
- Sponsored research agreements
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Build andmaintaintechnical and clinicalexpertisewithin your area through activities such as:
- Reviewing scientific literature
- Conducting customer interviews
- Attending conferences
- Visiting clinical sites
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Apply an understanding of business priorities to help execute strategy and deliver results that support broader organizational goals.
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Use judgment, prior experience, analytical thinking, and guidance from others to recommend practical solutions, including those that may extend beyond standard approaches.
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Collaborate closely with internal partners across engineering, regulatory, quality, and marketing, as well as with external clinical professionals.
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Contribute as a strong individual team member and, where applicable, provide informal mentorship, guidance, andknowledge-sharingto more junior colleagues.
Required qualifications
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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
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3+ years of molecular imaging Software as a Medical Device experienceOR 5+ years of closely related adjacent experience
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Strong problem-solving and analytical skills
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Ability to communicate and collaborate effectively with:
- Clinical professionals
- Engineering, regulatory, quality, and other cross-functional internal teams
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Demonstrated ability and aptitude to build clinical, anatomical, and technical domain knowledge
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Willingness to travel periodically for medical conferences, customer meetings, and site visits
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Legal authorization to work in the U.S. without current or future visa sponsorship
Preferred qualifications
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Master’s degree or PhD in a relevant field
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Prior experience in the software or medical device industry; strong familiarity with design controlsand regulatory submissions
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Direct experience withimaging software
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Strong technical writing skills
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Strong communicationskills, 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
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Experience working successfully in team-based environments
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Project management skills, including planning, documentation, and execution
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Experience mentoring junior engineers, delegating appropriately, and supporting team growth
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Recognized depth ofexpertisein advanced molecular imaging software
What will help you succeed in this role
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A proactive, growth-oriented mindset
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Curiosity and a thoughtful approach to investigating complex problems
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The ability to analyze challenges and develop effective solutions
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Strong written, verbal, and technical communication skills
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A collaborative working style and commitment to shared outcomes
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Interest in continuous learning and deepening your clinical and technicalexpertise
Why this role matters
This is an opportunity to help shape products that support clinicians and improvethe patientexperience. Your work will contribute to technologies used in complex clinical scenarios, and your voice will help influence how products evolve over time.You’lljoin a collaborative environment where clinical insight, technical innovation, and cross-functional partnership all playan important rolein delivering meaningful healthcare impact.
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 25, 2026
Originally posted on Himalayas
To apply for this job please visit himalayas.app.
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