Manufacturing Engineer II: Medical Device Process Innovator

Zimmer Biomet; United States; On-site; USD 70,000 - 90,000; Full time

Job summary

Zimmer Biomet in the United States is seeking a Manufacturing Engineer II to support efficient manufacturing processes, including cell management, process development, and tooling design.

You will drive feasibility studies, optimize methods, and partner with cross-functional teams to deliver on project plans while mentoring entry-level engineers. This role emphasizes quality, safety, and compliance within a global medical technology company.

Qualifications

• B.S. in Engineering with a minimum of 1 year of engineering experience.
• Familiarity with geometric dimensioning and tolerancing (GD&T).

Responsibilities

• Maintain and improve controlled technical documents such as prints, procedures, bills of materials and routers.
• Support machining, finishing, forging, casting, cleaning, heat treating, bonding, molding, etc.
• Conduct feasibility studies to estimate product cost and analyze capital equipment, capacity, and capability requirements.
• Improve process methods to meet performance and quality requirements.
• Execute to project plans and schedules for work activities.
• Communicate with appropriate personnel from other departments.
• Partner with cross-functional departments to make process and procedure recommendations.
• Provide training and guidance to entry-level engineers.

Skills

GD&T

Quality tools

Cross-functional teamwork

Problem-solving

Written communication

Verbal communication

Initiative

Training & guidance

Education

B.S. in Engineering

Tools

MS Office Suite

Microsoft Project

Job description

Zimmer Biomet in the United States is seeking a Manufacturing Engineer II to support efficient manufacturing processes, including cell management, process development, and tooling design.

You will drive feasibility studies, optimize methods, and partner with cross-functional teams to deliver on project plans while mentoring entry-level engineers. This role emphasizes quality, safety, and compliance within a global medical technology company.