Systems Sr Engineer
Zimmer Biomet
Senior Systems 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
We are looking for a Senior Systems Engineer. 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
- 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
- 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 priorities
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 requirements generation and trace matrices
- 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
Required:
- Bachelor's Degree and 4 years of relevant experience or equivalent experience required.
- Past experience working in the Medical Device Industry
Preferred:
- BS degree in Engineering (Biomedical, Electrical, or Computer Science)
- Work experience in a medical robotics
- Ability to create 3D models and 3D animations
Physical Requirements
Travel Expectations
Up to 20% both locally and internationally
EOE/M/F/Vet/Disability
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