Medical Device R&D Engineer II: Design & Prototyping

Aptyx; Charlotte (NC); On-site; USD 80,000 - 95,000; Full time

Job summary

A medical device company in Charlotte is seeking an R&D Engineer II to contribute to medical device product development. This role includes designing devices, performing hands-on assembly, supporting manufacturing readiness, and collaborating with cross-functional teams. The ideal candidate has a relevant degree, over 3 years of engineering experience in medical devices, and proficiency in SolidWorks. This opportunity involves working in a regulated environment and contributing to continuous improvement initiatives.

Qualifications

• 3+ years of engineering experience in medical device development or regulated manufacturing environment.
• Experience with catheter-based or complex medical device development strongly preferred.

Responsibilities

• Develop and engineer medical devices from concept through production with little supervision.
• Perform hands‑on product assembly and process development for catheters and other medical devices.
• Design and develop pilot and production tooling, fixtures, equipment.

Skills

Proficiency in SolidWorks or equivalent CAD software

Strong experience in hands‑on prototyping and mechanical assembly

Knowledge of medical device materials and manufacturing processes

Strong analytical and problem‑solving skills

Excellent verbal and written communication skills

Education

Bachelor's or Master's degree in Biomedical Engineering, Mechanical Engineering, or related discipline

Tools

Microsoft Office Suite

Job description

A medical device company in Charlotte is seeking an R&D Engineer II to contribute to medical device product development. This role includes designing devices, performing hands-on assembly, supporting manufacturing readiness, and collaborating with cross-functional teams. The ideal candidate has a relevant degree, over 3 years of engineering experience in medical devices, and proficiency in SolidWorks. This opportunity involves working in a regulated environment and contributing to continuous improvement initiatives.