Manager, Quality Systems

Role: Manager, Quality Systems within QA, overseeing Veeva electronic Document and Quality Management systems (QDocs, Training, eQMS, RIM). Objectives include system administration, configuration, access management, compliance assurance, and support for continuous improvement of quality workflows. Responsibilities encompass managing user roles, configuring Vault modules, supporting system updates and user testing, maintaining document workflows, supporting electronic signatures, and assisting in audits and regulatory inspections. Requirements: Bachelor's degree, 8+ years in biotech/pharma with at least 4 years in QMS functions, extensive Veeva Vault administration experience, preferably certified (e.g., Veeva Vault Admin). Strong knowledge of GxP, document control, and quality processes. Preferred: experience with system migrations, Vault implementations, EDMS platforms like PromoMats, and document archiving. High-value specifics: focus on GxP compliance, cGMP, Veeva Vault platform, and audit support; travel up to 10%. No sponsorship; salary range $100K–$145K.