[Remote] Senior Clinical Engineer – RO & GIP
Note: The job is a remote job and is open to candidates in USA. GE HealthCare’s MIM Software business is focused on developing vendor-neutral imaging software to enhance clinical workflows and patient care. The Senior Clinical Engineer will guide the clinical development of imaging products and Software as a Medical Device, ensuring safety and effectiveness while collaborating with multidisciplinary teams to drive product innovation.
Responsibilities
- 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
Skills
- 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
- 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
Benefits
- Performance based incentive compensation, which may include cash bonus(es) and/or long term incentives (LTI)
- Medical, dental, vision, paid time off, a 401(k) plan with employee and company contribution opportunities, life, disability, and accident insurance, and tuition reimbursement
- Relocation Assistance Provided
Company Overview