MedTech Design Engineer — Product Development (0–5 yrs)

Enexor BioEnergy, LLC; Franklin (VA); On-site; USD 70,000 - 100,000; Full time

Benefits offered by this job

Competitive salary

Equity

Health insurance stipend (QSEHRA)

401(k)

Paid vacation and holidays

Front row seat in a fast-growing med/‑

Job summary

Enexor BioEnergy, LLC is seeking Mechanical or Biomedical Engineers to design and develop a new Class II medical device from concept through FDA submission. You will work hands-on from CAD to verification and validation, collaborating across disciplines in a fast-paced startup.

The role emphasizes prototyping, testing, and documentation under FDA design control, with opportunities to influence risk analysis, labeling, and regulatory paperwork while enjoying equity potential and a collaborative

Qualifications

• B.S./M.S. in Mechanical or Biomedical Engineering.
• Strong fundamentals in fluid dynamics and pressure systems.
• Hands-on prototyping or lab testing experience.
• Curious, adaptable, and fast learner in a collaborative team.

Responsibilities

• Design and model mechanical subsystems and assemblies using Autodesk Inventor.
• Build and test prototypes for airflow, pressure, vibration, and structural performance.
• Support DFM, BOM creation, and documentation under FDA design control.
• Participate in bench and environmental testing for verification and validation.
• Collaborate with electrical, firmware, and manufacturing teams to integrate systems.
• Contribute to risk analysis, labeling, and regulatory documentation.

Skills

Fluid dynamics

Pressure systems

Mechanical design

Prototyping

Education

B.S./M.S. in Mechanical or Biomedical Engineering

Tools

Autodesk Inventor

Job description

Enexor BioEnergy, LLC is seeking Mechanical or Biomedical Engineers to design and develop a new Class II medical device from concept through FDA submission. You will work hands-on from CAD to verification and validation, collaborating across disciplines in a fast-paced startup.

The role emphasizes prototyping, testing, and documentation under FDA design control, with opportunities to influence risk analysis, labeling, and regulatory paperwork while enjoying equity potential and a collaborative