Systems Principal Engineer

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 talent 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 included, respected, empowered and recognised.

What You Can Expect

In this role you will work with Project Management, Regulatory, Quality, Electrical, Mechanical, and Software teams to create requirements from User Needs, perform Systems and Risk Analysis, and create V&V Plans, Protocols, and Reports. You will also perform summative and formative evaluation and design verification tests.

Monogram''s surgeon-guided semi- and fully autonomous robotic technologies are expected to add new and differentiated capabilities to Zimmer Biomet''s already broad suite of customer-centric technology solutions. By joining this team you will be taking part in cutting edge technology used to improve patient outcomes and relieve pain for patients across the globe. Excited to join us? Submit your application now.

How You'll Create Impact

• Independently design complex systems, including system architectural design, relevant design documentation, test planning, and execution
• Translate customer and system requirements into subsystem and component-level requirements
• Be able to speak directly with Surgeons and work within a cadaver lab environment
• Support and execute segments of complex product development to advance projects through the design /development/V&V/launch process
• Lead Hazards Analysis to create the project's FMEA
• Plan and execute verification protocols
• Generate and review necessary documents with project teams (requirements, design, architecture, bugs, tests)
• Demonstrate advanced understanding of customer needs and design inputs.•Demonstrate proficiency with the product's intended use and clinical procedures.
• Identify and support the creation of procedures, policies, processes, systems, and technology
• Work cooperatively with Project Management, Quality, Manufacturing, Regulatory, Mechanical, Electrical, Software, Clinical, and Marketing to ensure project success as a leader on the team
• Demonstrate ownership and integrity of work.

What Makes You Stand Out

• Strong writing skills for protocols and reporting
• Past Development exposure, with basic level knowledge of how to read code
• SolidWorks experience
• Work with Medical Device Robotics
• Exposure to Cadaver labs and gathering design feedback from a Surgeon
• Experience in systems analysis using MBSE software
• Experience in Hazards Analysis and FMEA generation
• Experience using Application Lifecycle Management /Traceability tools
• Experience with regulatory and compliance standards
• Familiarity with a variety of sensor, actuator, motor, and controller technologies

Your Background

• Preferred Qualification: Ability to create 3D models and 3D animations
• Preferred Qualification: Work experience in a medical device company with a focus on robotics
• Preferred Qualification: Masters or PhD degree in Engineering (Biomedical, Electrical, or Computer Science)
• Minimum Qualification: Bachelor''s Degree and 6 years of relevant experience, or Associate''s Degree and 8 years of relevant experience, or High School Diploma or Equivalent and 10 years of relevant experience

Physical Requirements

Travel Expectations

• Up to 20% both local and international

EOE/M/F/Vet/Disability