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
Job Summary
As the Senior Systems Engineer, you will work with Project Management, Regulatory, Quality, Electrical, Mechanical, and Soware teams to create requirements from User Needs, perform Systems and Risk Analysis, and create V&V Plans, Protocols, and Reports. You will then perform summave and formave evaluaons and design verificaon tests.
How You'll Create Impact
Essenal Dues & Responsibilies
- Independently design complex systems, including system architectural design, relevant design documentaon, test planning, and execuon
- Translate customer and system requirements into subsystem and component-level requirements
- 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 verificaon 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.
- Idenfy and support the creaon of procedures, policies, processes, systems, and technology
- Work cooperavely with Project Management, Quality, Manufacturing, Regulatory, Mechanical, Electrical, Soware, Clinical, and Markeng to ensure project success as a leader on the team
- Learn procedures, policies, processes, systems, and technology required
- Demonstrate ownership and integrity of work.
- Deliver high-quality results with passion, energy, and drive to meet business priories
What Makes You Stand Out
Strong writing skills for protocols and reportingPast Development exposure, with basic level knowledge of how to read codeSolidWorks experienceWork with Medical Device RoboticsWork within a Cadaver Lab strongly preferredHigher education Degree (Master's or PhD)Your Background
Qualificaons and Work Experience Required
BS degree in Engineering (Biomedical, Electrical, or Computer Science preferred)3+ years of work experience in a medical device company; robotics is preferredMust have exposure to Cadaver labs and gathering design feedback from a SurgeonExperience in systems analysis using MBSE sowareExperience in requirements generaon and trace matricesExperience in Hazards Analysis and FMEA generaonExperience using Applicaon Lifecycle Management / Traceability toolsExperience with regulatory and compliance standardsFamiliarity with a variety of sensor, actuator, motor, and controller technologiesPhysical Requirements
Travel Expectations
Up to 20% both local and international
EOE / M / F / Vet / Disability