Demo

Product Development Engineer II

Zimmer Biomet
Englewood, CO Full Time
POSTED ON 5/9/2026
AVAILABLE BEFORE 6/7/2026
At Zimmer Biomet, we believe in pushing the boundaries of innovation and driving our mission forward. As a global medical technology leader for nearly 100 years, a patient’s mobility is enhanced by a Zimmer Biomet product or technology every 8 seconds.

As a Zimmer Biomet team member, you will share in our commitment to providing mobility and renewed life to people around the world. To support our talented team, we focus on development opportunities, robust employee resource groups (ERGs), a flexible working environment, location specific competitive total rewards, wellness incentives and a culture of recognition and performance awards. We are committed to creating an environment where every team member feels inspired, invested, cared for, valued, and have a strong sense of belonging.

What You Can Expect

Ready to lead the next breakthrough in foot and ankle innovation? Paragon 28, a Zimmer Biomet company, is looking for a Product Development Engineer II to join our elite R&D team in Englewood, Colorado!

This isn't just a design job—it’s your chance to take ownership of meaningful projects that restore mobility and change lives. In this role, you’ll lead key aspects of the design life cycle, collaborating with a world-class project team to turn complex orthopedic challenges into cutting-edge medical solutions. As you prove your expertise, you’ll earn increasing autonomy to drive innovation and shape the future of our product portfolio.

Why Paragon 28?

  • Purpose-Driven Work: Every device you develop helps a patient get back on their feet.Professional Growth:
  • Gain hands-on leadership experience with a clear path to independent project ownership.
  • Collaborative Culture: Work alongside the best in the industry in a fast-paced, high-impact R&D environment.

If you’re a problem-solver ready to elevate your engineering career and leave a lasting mark on the medtech world, we’re ready for you. Apply today!

How You'll Create Impact

  • Produce deliverables in a product development leading role from ideation to commercialization through entire product life cycle and on a given timeline, as directed by senior engineering staff, including:
    • Research and evaluate competitive product for performance characteristics
    • Conceptualization of new design ideas with some understanding of the inadequacy of existing designs
    • Parametric modeling and detail design of P28 implant and instrument development
    • Work within the P28 product development procedure to create design control documentation for P28 design history files.
    • Participate in development of testing protocols and assist in the testing process for new and existing products
    • Compile and comprehend test results and implement/recommend appropriate design changes
    • Lead activities related to project phase gate design reviews
    • Interface with 3rd party suppliers, contractors, testing houses, etc.
  • Assist the P28 Quality and Supply Chain departments to evaluate new suppliers for inclusion in the P28 approved supplier list
  • Assist P28 Quality team in developing inspection plans
  • Aide in publication efforts with Clinical Affairs team
  • Observe surgery (live, cadaver, or video) on lower extremity pathology and formulate physician comments/ideas into meaningful design solutions. Document all notes.
  • Serve as technical expert resource within specific product categories for Sales Support and other departments via phone and live product training.
  • Assist on patent application preparation
  • Assist with other development projects as additional resource when needed, while balancing own workload
  • Other duties as directed by manager
Your Background

  • Requires a bachelor’s degree in Mechanical Engineering, Biomedical Engineering or related engineering discipline with 3-7 years of development experience in medical device.
  • Prior experience in taking medical device from ideation to commercialization required.
  • Understanding of medical device industry regulatory requirements preferred.
  • Experience with CAD. SolidWorks preferred.
  • High proficiency in MS Office
  • Effective communication and presentation skills with ability to convey information and respond to questions from groups of peers
  • Ability to work in a team environment

Travel Expectations

Up to 10% of overnight travel.

Compensation Data

Salary Range: $80,000 - $100,000 depending on skills and experience

EOE

Salary : $80,000 - $100,000

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