Document Control Assoc Specialist

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.

Responsibilities

• 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

Requirements

• 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

Compensation: $51,000-$63,000 USD