Senior Mechanical Engineer – Intraoperative Neuromonitoring

NML Medical; Pennsylvania; On-site; USD 110,000 - 160,000; Full time

Job summary

Globus Medical is seeking a Sr. Mechanical Engineer to join our R&D team focused on intraoperative neuromonitoring systems for spinal and cranial surgeries.

You will lead mechanical design and development for both sustaining products and next-gen NPI projects, collaborating with Regulatory, Quality, Supply Chain, and Manufacturing to ensure safe, effective, and compliant clinical solutions. Responsibilities include managing feasibility studies, maintaining design history documents, and

Qualifications

• Minimum 5–7 years of related experience.
• Bachelor's or advanced degree in Mechanical or Biomedical Engineering.
• Proficiency with CAD and SolidWorks; familiarity with Pro/E or Creo.
• Strong ability to write technical reports and communications.
• Knowledge of manufacturing processes and design for manufacturing.
• Experience with FDA and ISO 13585 & IEC 60601 compliance.

Responsibilities

• Leads mechanical design & development for NPI and Sustaining projects.
• Creates advanced mechanical designs using CAD/SolidWorks and rapid prototyping.
• Coordinates with suppliers and supply chain to manage production and commercialization; drives cost optimization.
• Creates and maintains design history files and design controls documentation.
• Works with surgeons and OR staff to understand user needs.
• Participates in project planning, design reviews, and audits.

Skills

CAD

SolidWorks

Microsoft Office

Education

Bachelor's degree in Mechanical Engineering

Bachelor's degree in Biomedical Engineering

Tools

Pro/E

Creo

SolidWorks

Job description

Globus Medical is seeking a Sr. Mechanical Engineer to join our R&D team focused on intraoperative neuromonitoring systems for spinal and cranial surgeries.

You will lead mechanical design and development for both sustaining products and next-gen NPI projects, collaborating with Regulatory, Quality, Supply Chain, and Manufacturing to ensure safe, effective, and compliant clinical solutions. Responsibilities include managing feasibility studies, maintaining design history documents, and