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Mechanical Engineer

Job in Atlanta, Fulton County, Georgia, 30319, USA
Listing for: Kelly
Full Time position
Listed on 2026-09-05
Job specializations:
  • Engineering
    Mechanical Engineer
Job Description & How to Apply Below

Mechanical Engineer

Mechanical Engineer - Medical Devices, Direct Hire. (Duluth, GA)

We are seeking a highly experienced Mechanical Engineer to provide hands-on design and development of next-generation battery-powered orthopedic surgical power tools.

Position Summary:

As a core member of our Engineering group, you will take ownership of designing, prototyping, and testing novel medical devices and fixtures. This is a highly hands-on role where you will bridge the gap between mechanical design, electrical prototyping, and rigorous regulatory compliance. You will work closely with electrical engineers, quality assurance, and clinical specialists to ensure our products exceed the highest standards of safety, quality, and efficacy.

New role created due to growth.

Key Responsibilities:

Mechanical Design & CAD:
Create detailed 3D models, complex assemblies, and production-ready drawings using Solid Works. Utilize the principles of Design for Manufacturing (DFM) and Design for Assembly (DFA) concerning CNC machining, injection molding, and material biocompatibility. Tolerance Analysis:
Perform rigorous tolerance stack-up analyses incorporating GD&T (Geometric Dimensioning and Tolerancing) principles to ensure optimal fit, form, and function. Prototyping:
Rapidly iterate designs utilizing internal 3D printing technologies and traditional workshop tools. Fixture Design & Build:
Design and build custom hands-on test fixtures to support verification and validation testing. Incorporate basic electrical circuit design, including working with microcontroller (i.e. Arduino) circuits for electromechanical operation. Testing & Documentation:
Author comprehensive test protocols and reports to support design verification and engineering studies. Regulatory Compliance:
Ensure all design and documentation practices strictly align with 21 CFR Part 820 (Quality System Regulation), ISO 13485, and ISO 14971 standards.

Required

Qualifications & Skills:

Education:

Bachelor's degree in Mechanical Engineering, Biomedical Engineering, or a related technical discipline.

Experience:

3+ years of professional engineering experience within the medical device field.

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