Quality Sr Engineer I - Robotics Manufacturing & System Integration

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

In this role, you will serve as a Senior Quality Engineer I supporting contract manufacturing operations for surgical robotic systems. You will ensure the successful installation, calibration, validation, and final quality control of SiMD robotic cart systems and tracker stands at a contract manufacturer site in Milwaukee, WI.

You will work hands-on with complex electromechanical and software-integrated medical devices, ensuring all systems meet Zimmer Biomet specifications, regulatory requirements, and release criteria.

This position is onsite, 5 days per week in Milwaukee, WI.

How You'll Create Impact

Lead onsite quality engineering activities for SiMD robotic cart and tracker stand systems at contract manufacturer facilities

Oversee and execute clinical software installation and configuration on robotic carts and display systems

Perform and/or validate robotic arm, camera (infrared tracker), and system-level calibrations

Ensure completion and compliance of system integration verification and validation activities

Execute and approve final QC testing, including:

Electrical safety and functional testing

Software/applicative system testing

Hardware/system integration verification

Collaborate with Manufacturing, R&D, Software, and Supplier Quality teams to resolve issues and drive product readiness

Author and maintain quality documentation, test procedures, calibration records, and device history records (DHRs)

Support nonconformance investigations, root cause analysis, and CAPA activities

Ensure contract manufacturer adherence to ZB quality requirements, QSR, and ISO 13485 standards

Provide technical guidance and training to manufacturing personnel

Participate in internal/external audits (FDA, notified bodies, suppliers)

What Makes You Stand Out

Strong hands-on experience with robotic systems, electromechanical assemblies, or imaging systems

Experience with system integration, calibration processes, and software-hardware interfaces

Ability to troubleshoot complex systems involving robotics, sensors, and software applications

Strong knowledge of medical device regulations (FDA QSR, ISO 13485)

Familiarity with electrical safety standards and system-level verification testing

Knowledge of validation (IQ/OQ/PQ), calibration methods, and quality tools (FMEA, CAPA, DMAIC)

Excellent problem-solving skills and ability to work independently in a manufacturing environment

Effective communication and cross-functional collaboration skills

Applicable Regulatory & Consensus Standards

Ensure compliance with FDA and EU MDR requirements by applying relevant recognized consensus standards for medical robotic systems and SiMD, including:

Quality & Risk Management

ISO 13485 – Medical Device Quality Management Systems

ISO 14971 – Application of Risk Management to Medical Devices

Software & SiMD

IEC 62304 – Medical Device Software Lifecycle Processes

FDA Guidance on Software as a Medical Device (SaMD) and cybersecurity

IEC 82304-1 – Health software product safety

Usability & Human Factors

IEC 62366-1 – Usability Engineering

Electrical & System Safety

IEC 60601-1 – General Requirements for Basic Safety and Essential Performance

IEC 60601-1-2 – Electromagnetic Compatibility

IEC 60601-1-6 – Usability (aligned to IEC 62366)

Robotics & Complex Electromechanical Systems

ISO 10218-1 / 10218-2 – Safety Requirements for Industrial Robots (as applicable to collaborative systems)

IEC 80601 (where applicable for medical electrical equipment systems)

EU MDR Compliance

Regulation (EU) 2017/745 (MDR) – General Safety and Performance Requirements (GSPR)

MEDDEV & MDCG guidance (clinical evaluation, software qualification, cybersecurity)

Your Background

Minimum Requirements: Bachelor's Degree in Engineering and 3 years of relevant experience

Bachelor’s degree in Mechanical, Electrical or Biomedical Engineering preferred

3+ years of experience in Quality Engineering or Manufacturing Engineering in medical devices or regulated industries preferred

Experience with robotic systems, software-controlled devices, or capital equipment preferred

Experience working with contract manufacturers and supplier environments preferred

Travel Expectations

Up to 25% travel (primarily between Zimmer Biomet sites and Milwaukee contract manufacturer)

EOE