Product Project Engineer

About Dilon Technologies

Dilon Technologies is an innovative medical device company headquartered in Newport News, Virginia, dedicated to advancing breast health and improving patient outcomes. Our portfolio of cutting-edge technologies, including Margin Probe®, Navigator®, and True View®, helps physicians make more informed decisions and deliver exceptional patient care.

At Dilon, we're passionate about making a difference. Our team thrives on innovation, collaboration, and a shared commitment to bringing meaningful medical technologies to market. We offer a dynamic, hands-on environment where employees can take ownership, contribute ideas, grow professionally, and see the direct impact of their work.

If you're motivated, enjoy a challenge, and want to be part of a team where your contributions truly matter, we'd love to hear from you!

Product / Project Engineer

Dilon Technologies | Engineering | Full-time | On-site

Dilon Technologies is looking for a Product / Project Engineer to help take our next-generation medical devices from concept through production. You’ll work directly with the VP of Engineering to turn product ideas into clear requirements, keep development projects on track, and write the design documentation and V&V protocols that get products through design controls.

This is a hands-on, cross-functional role on a small engineering team. You’ll work with hardware, software, mechanical/manufacturing, and test engineers every day, and you’ll get broad exposure to the whole product lifecycle. It’s a strong fit for an engineer who likes seeing how all the pieces fit together and wants to grow toward systems engineering or project leadership.

• Requirements: Work with the team to translate user needs and product goals into clear, testable product and subsystem requirements.

• Project coordination: Plan and track development projects: build schedules, track tasks and action items, flag risks early, and keep work moving across disciplines.

• V&V protocols: Write V&V plans and protocols with clear acceptance criteria and traceability to requirements and risk controls.

• Testing and reporting: Coordinate test execution with our test engineer/technician and external test labs; write test reports and document deviations.

• Traceability: Maintain requirements traceability from user needs through design inputs, outputs, risk controls, and verification evidence.

• Risk management: Create risk management files per ISO 14971, including hazard analyses and FMEAs.

• Design controls: Build and maintain DHF content, prepare design review packages, and help turn engineering work into clear, compliant documentation.

• Standards testing: Help plan and coordinate testing to standards such as IEC 60601-1 and IEC 60601-1-2, including scheduling and working with external test labs.

• Change and investigations: Support ECOs, anomaly investigations, and CAPAs, including impact assessments and documentation.

• Design transfer: Support design transfer with manufacturing engineering, including pilot builds and production readiness.

• Communication: Serve as a day-to-day point of contact for suppliers, contract partners, and internal teams on project status and technical questions.

• Bachelor’s degree in engineering (any discipline: Electrical, Mechanical, Biomedical, Systems, or related).

• [2–5] years of engineering experience, preferably in medical devices or another regulated industry.

• Exposure to design controls (21 CFR 820 / ISO 13485) and risk management (ISO 14971).

• Experience writing technical documents such as test protocols, test reports, or requirements.

• Strong technical writing. You can produce clear, organized documentation that others…