Engineering Manager, Knee NPD & MedTech Innovation

Enovis Corporation; Austin (TX); Hybrid; USD 140,000 - 190,000; Full time

Benefits offered by this job

Medical Insurance

Dental Insurance

Vision Insurance

401(k) Plan

Vacation, Sick Leave, and Holidays

Job summary

Enovis Corporation in Austin, Texas, seeks an Engineering Manager for Knees to guide biomedical and mechanical engineers in the full development cycle of knee implants—from concept to commercialization. This role leads design, validation, documentation, and risk assessment while coordinating with surgeons, manufacturing, and suppliers.

You will mentor teams, drive project schedules and budgets, and ensure Regulatory and Quality requirements are met in a fast-paced medical device environment,

Qualifications

• 10+ years of design/development experience in medical devices or orthopedics is required.
• Strong leadership and mentoring skills with a track record of delivering complex programs.
• Experience applying FDA and ISO regulations and internal procedures to product development.
• Ability to communicate effectively with cross-functional teams and leadership.

Responsibilities

• Lead biomedical/mechanical engineers and technicians in bringing new knee products to market.
• Oversee concept through commercialization, including risk assessments and design history files.
• Collaborate with Manufacturing, Regulatory, Purchasing, and Quality to ensure schedules and budgets are met.
• Model-based design work (3D CAD) and documentation for device development.
• Manage internal and external design, development, testing, and manufacturing suppliers.

Skills

Leadership

Cross-functional collaboration

Regulatory knowledge

Presentation skills

Education

BS in Mechanical Engineering

Tools

SolidWorks

NX

Pro/Engineer (ProE)

Job description

Enovis Corporation in Austin, Texas, seeks an Engineering Manager for Knees to guide biomedical and mechanical engineers in the full development cycle of knee implants—from concept to commercialization. This role leads design, validation, documentation, and risk assessment while coordinating with surgeons, manufacturing, and suppliers.

You will mentor teams, drive project schedules and budgets, and ensure Regulatory and Quality requirements are met in a fast-paced medical device environment,