Medical Device Design Engineer - Concept to FDA Submission

LaunchTN; Franklin (TN); On-site; USD 60,000 - 90,000; Full time

Benefits offered by this job

Salary + equity

Health stipend (QSEHRA)

401(k)

Paid vacation

Job summary

LaunchTN seeks Mechanical or Biomedical Engineers, recent graduates or with up to five years of experience, to design and develop a new Class II medical device from concept through FDA submission. You will be involved in CAD modeling, prototyping, system integration and V&V.

Responsibilities include using Autodesk Inventor to model subsystems, building prototypes, supporting DFM and BOM, and contributing to regulatory documentation in a fast-paced, collaborative setting.

Qualifications

• B.S. or M.S. in Mechanical or Biomedical Engineering.
• Strong fundamentals in fluid dynamics, pressure systems, and mechanical design.
• Hands-on experience with prototyping or lab testing.
• Curious, adaptable, and motivated to learn in a fast-paced, collaborative environment.

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

Prototyping

Lab testing

Mechanical design

Team collaboration

Education

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

Tools

Autodesk Inventor

Job description

LaunchTN seeks Mechanical or Biomedical Engineers, recent graduates or with up to five years of experience, to design and develop a new Class II medical device from concept through FDA submission. You will be involved in CAD modeling, prototyping, system integration and V&V.

Responsibilities include using Autodesk Inventor to model subsystems, building prototypes, supporting DFM and BOM, and contributing to regulatory documentation in a fast-paced, collaborative setting.