
Senior Clinical Engineer β RO, GIP
Posted 9 hours ago

Posted 9 hours ago
This is a fully remote position, open to applicants in Ohio.
β’ Assist in the clinical development of imaging products, diagnostics, and Software as a Medical Device by evaluating safety, effectiveness, and clinical value.
β’ Convert clinical and customer requirements into functional specifications that guide product development.
β’ Engage in software prototyping, support verification and validation (V&V) testing, and facilitate iterative enhancements post-product launch.
β’ Lead and participate in cross-functional projects that promote product success, including tasks related to: Product roadmap execution, product lifecycle planning, Software as a Medical Device regulatory submissions (such as 510(k)), and Sponsored research agreements.
β’ Develop and sustain technical and clinical expertise in your domain by performing activities like: Reviewing scientific literature, conducting customer interviews, attending conferences, and visiting clinical sites.
β’ Utilize an understanding of business priorities to assist in executing strategy and achieving results that align with broader organizational objectives.
β’ Exercise judgment, prior experience, analytical reasoning, and guidance from others to propose practical solutions, including those that may go beyond conventional methods.
β’ Collaborate effectively with internal partners across engineering, regulatory, quality, and marketing, as well as with external clinical professionals.
β’ Contribute as a valuable individual team member and, when appropriate, offer informal mentorship, guidance, and knowledge-sharing to less experienced colleagues.
β’ Bachelorβs degree from an accredited institution in a relevant field such as Biomedical Engineering, Radiologic Technology or Radiologic Sciences, Computer Science, Medical Physics, or a related discipline.
β’ 3+ years of experience in molecular imaging Software as a Medical Device OR 5+ years of closely related experience.
β’ Strong analytical and problem-solving abilities.
β’ Capacity to communicate and collaborate effectively with clinical professionals, engineering, regulatory, quality, and other cross-functional internal teams.
β’ Proven ability and aptitude to develop clinical, anatomical, and technical domain knowledge.
β’ Willingness to travel occasionally for medical conferences, customer meetings, and site visits.
β’ Legal authorization to work in the U.S. without current or future visa sponsorship.
β’ Health insurance.
β’ 401(k) plan with options for employee and company contributions.
β’ Paid time off.
β’ Tuition reimbursement.
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