Quality Systems Specialist

To support a company in the life sciences industry, the remote Quality Systems Specialist will manage document control processes, coordinate change control activities, and maintain compliance with quality system requirements on a 6-month contract basis. Key responsibilities Manage the routing and approval of controlled documents, ensuring compliance and timely completion Coordinate administrative activities related to change control within an electronic Quality Management System (eQMS) Maintain organized and audit-ready quality documentation while supporting compliance with regulatory requirements Required qualifications Associate degree required; Bachelor's degree preferred in Quality, Life Sciences, Business Administration, or a related field 5+ years of experience in document control, quality systems, and change control within a regulated environment Hands-on experience with Veeva Vault QualityDocs or similar electronic document management systems Extensive experience coordinating change controls and document review workflows Strong understanding of Good Documentation Practices (GDP) and quality system requirements