Document Control Assoc Specialist
Zimmer Biomet · Warsaw, IN
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Role summary
Document Control Associate Specialist role at Zimmer Biomet focused on executing document control and records management processes in a medical device quality environment. Responsible for processing and maintaining records, training peers, developing procedures, and managing change control to ensure regulatory compliance.
What they're looking for
- Bachelor's degree in engineering, business, life sciences, or similar discipline
- 1-3 years quality control, quality assurance, or compliance experience
- Knowledge of 21 CFR Parts 11 and 820, including ISO 13485 QMS
- Proficiency in Microsoft Office and SharePoint
- Strong writing, editing, and attention to detail skills
- Electronic Document Management (eDM) systems experience preferred
- Compliance audit or inspection participation experience preferred
What you'll be doing
- Execute document control and records management processes with appropriate retention and updates
- Train team members on various processes and procedures
- Author and develop new documents and operational processes
- Manage change control processes and meetings to ensure timely request processing
- Identify and drive departmental process improvement projects
Compensation$51,000-$63,000 USD
Privacy & handoff
This role links to Zimmer Biomet's own application system. RoleLantern records your interest and checks the link, but the application happens on the employer's site and status updates may not come back to us. Clicking apply does not mark you as applied automatically.