Manager, Quality Systems

Role: Manager of Quality Systems within the QA department, supporting Veeva electronic Document and Quality Management systems (QDocs, Training, eQMS, RIM). Responsibilities: system administration, user access management, configuration support, workflow and document lifecycle management, training support, document archiving, and continuous system improvement. Collaborate cross-functionally, participate in audits and regulatory inspections, ensure GxP and cGMP compliance. Requirements: Bachelor’s degree, 8+ years in biotech/pharma industry with at least 4 years in QMS functions, extensive Veeva Vault administration experience, Veeva Vault Certification preferred, strong understanding of GxP processes within Veeva modules, proficiency in MS Office. Preferred: experience in system migrations, document archiving, and EDMS systems like PromoMats. High-Value: focus on GxP compliance, cGMP in biotech/pharma, Veeva Vault administration, regulatory audits, and cross-functional collaboration. Work setup: not specified; travel up to 10%.