About the position
RIVANNA is seeking a Product Development Engineer to join our dynamic engineering team. You will work with a talented team of professionals as we strive to achieve our mission to develop and commercialize world-first imaging-based medical technologies that elevate global standards of care. As a Product Development Engineer, you will contribute to activities across the product lifecycle, from prototype development to clinical support. This hands-on multidisciplinary role involves close collaboration with the mechanical, manufacturing, and electrical engineering team on a wide range of product development tasks and projects. This job will be on-site in Charlottesville, VA; applicants must be local or willing to relocate to Charlottesville for this position.
Responsibilities
- Support the development and improvement of medical devices and manufacturing processes
- Design and execute test methods to verify subsystem and system performance, analyze data, and document results in test reports
- Operate and maintain 3D printers and machine shop equipment (e.g., mill, lathe, drill press) to support prototype and fixture fabrication
- Assist with the assembly of electromechanical systems for engineering builds, internal testing, and clinical evaluation
- Create and update design control and design transfer documentation including work instructions, BOMs, test plans, and test reports
- Provide technical support for systems in the field, including remote troubleshooting and occasional travel to clinical sites
- Work closely with engineering, production, and clinical teams to support product development and sustaining efforts
Requirements
- Bachelor’s degree in Biomedical Engineering, Mechanical Engineering, or a related engineering discipline
- 1-3 years of relevant industry experience in product development or R&D (medical device experience preferred)
- Hands-on experience with hand tools, power tools, 3D printing, soldering, and test equipment
- Experience with SolidWorks or similar CAD software preferred
- Exposure to medical device regulations and quality systems including ISO 13485, FDA design controls (21 CFR), and risk management processes (ISO 14971)
- Strong organizational, communication, and technical writing skills
- Ability to work independently and on cross-functional teams in a fast-paced environment
- Willingness to travel occasionally (=10%) for field service support
- Applicants must be authorized to work in the United States without the need for current or future sponsorship
Benefits
- Health insurance
- Vision and dental coverage
- Group life insurance
- Long-term disability insurance
- Paid time off
- 401(k) plan with company match
