Senior Medical Device R&D Engineer

Terumo Neuro; Aliso Viejo (CA); On-site; USD 140,000 - 190,000; Full time

Job summary

Terumo Neuro is seeking a senior engineer to lead development of medical device products, writing and verifying specifications, designing fixtures, and testing processes and materials to ensure prototypes meet requirements.

The role requires a Mechanical/Industrial/Materials Science background with 10+ years in medical devices, strong communication, and ability to lead cross-functional teams through regulatory submissions.

Qualifications

• Bachelor’s degree in mechanical engineering, industrial engineering, or materials science engineering.
• Minimum of ten years of relevant work experience in medical device industry.
• Strong written and verbal communication skills.
• Ability to design and develop medical devices.
• Ability to read and prepare technical documentation.
• Working knowledge of medical device manufacturing equipment/processes.
• Knowledge of medical and technical development.

Responsibilities

• Develop new product concepts across engineering disciplines and provide design and process development.
• Develop products, test methods, data engineering, and analytical capabilities.
• Specify and test new materials and designs.
• Coordinate with departments and outside services to modify designs.
• Support regulatory submissions and approvals.
• Lead projects and mentor Assemblers, Technicians, and others as needed.
• Lead test method development, data analysis, root cause investigations, and test reports.

Skills

Communication

Leadership

Education

Bachelor's degree in Mechanical Engineering/Industrial Engineering/Materials Science Engineering

Tools

MS Word

Excel

PowerPoint

Minitab

SolidWorks

CAD

Job description

Terumo Neuro is seeking a senior engineer to lead development of medical device products, writing and verifying specifications, designing fixtures, and testing processes and materials to ensure prototypes meet requirements.

The role requires a Mechanical/Industrial/Materials Science background with 10+ years in medical devices, strong communication, and ability to lead cross-functional teams through regulatory submissions.