Controlled Documents Specialist

To ensure compliance and efficient management of document lifecycles, the full-time Controlled Documents Specialist will oversee controlled documents within the Veeva Quality platform, supporting stakeholders and maintaining regulatory standards in a remote capacity. Key responsibilities Manage the lifecycle of controlled documents in Veeva, including creation, review, approval, and archival Ensure compliance of controlled documents with regulatory requirements and internal standards Support inspection readiness by maintaining organized and accessible controlled documents Required qualifications Bachelor's degree in Life Sciences or a related scientific field with 1-3 years of experience in a regulated environment Experience using electronic document management systems, preferably Veeva Experience supporting audits and inspections Understanding of controlled documents and quality management systems Proficiency in Microsoft Office