As a global medtech company, LivaNova is driven by its Vision of changing the trajectory of lives for a new day and its Mission to create ingenious solutions that ignite patient turnarounds. The Document Control Specialist is responsible for processing controlled documentation and maintaining the controlled documentation system. This role ensures that new, revised, and obsolete documents are processed accurately and efficiently through the document change control process in accordance with company procedures, FDA Quality System Regulations, ISO standards, and other applicable regulatory requirements. Other responsibilities include configuration management, role management, document control, and/or enterprise system data entry. The Document Control Specialist role performs document reviews for completeness, coordinates approvals, manages document metadata, and ensures timely release and distribution of controlled records. This role partners with cross-functional stakeholders to ensure documentation remains current, compliant, and accessible. This role may also perform limited training duties as back-up to the Training Coordinator(s).
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Job Type
Full-time
Career Level
Mid Level
Education Level
High school or GED