Job Information
Zimmer Biomet Quality Engineer II in Claymont, Delaware
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
Responsible for Document Control, Learning Management System and Equipment Control. Support Audit activities and incoming inspection. Interacts with many different functional departments, suppliers, and experts outside Zimmer Biomet to implement Zimmer Biomet Quality goals.
How You'll Create Impact
• Manage the approval process and release of documents within the Quality Management System
• Ensure all documents comply with internal quality standards and regulatory requirements.
• Coordinate document change requests (DCRs), Change request CRs, track progress, and communicate status updates to stakeholders.
• Support both internal and external audits from document control aspect
• Manage training assignments, curricula updates, and user access within the LMS.
• Ensure training records are complete, accurate, and audit‑ready.
• Monitor training compliance metrics and follow up with employees and supervisors as needed.
• Assist in developing and maintaining training materials and documentation.
• Maintain equipment inventory, calibration schedules, and maintenance records.
• Coordinate calibration, preventive maintenance, and equipment qualification activities with internal teams and external vendors.
• Ensure equipment status is accurately reflected in tracking systems and that all required documentation is complete.
This is not an exhaustive list of duties or functions and might not necessarily comprise all of the essential functions for purposes of the Americans with Disabilities Act.
What Makes You Stand Out
Ability to work within a team environment and build relationships outside of the department as well as outside the company (suppliers, regulatory agencies, etc.).
Good attention to detail
Ability to deliver, meet deadlines and have results orientation.
Able to communicate both orally and in written form to multiple levels of the company.
Demonstrates characteristics of high potential for future development opportunities.
Microsoft Office Suite.
Thorough understanding of QSR/ISO regulations.
Your Background
B.S. in engineering or an alternative Bachelor’s degree program with certification as a quality engineer (e.g. CQE).
Minimum 1 year of relevant work experience.
Certified Quality Engineer (CQE) and Medical device, particularly Orthopedic industry, experience preferred
Travel Expectations
Up to 20%
EOE/M/F/Vet/Disability