Posted Aug 29, 2026

Veeva QualityDocs & ComplianceWire Administrator (Consultant)

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Title: Veeva QualityDocs & ComplianceWire Administrator (Consultant) Location: Remote Duration: Consultant / Contract We are seeking an experienced Veeva Administrator Consultant to support and manage our Veeva QualityDocs (QDocs) and ComplianceWire LMS platforms. This consultant will act as a subject matter expert, owning day-to-day administration, user support, document lifecycle management, and training compliance activities. The ideal candidate has deep, hands-on experience in GxP-regulated environments and is comfortable working independently while partnering closely with Quality, Regulatory, and Clinical Operations teams in a fast-moving clinical-stage biotech setting. • *Must have extensive experience with both Veeva QualityDocs (QDocs) and ComplianceWire LMS. Key Responsibilities: Veeva QualityDocs (QDocs) Administration • Serve as SME and primary administrator for Veeva QualityDocs. • Configure and manage document lifecycles, workflows, templates, and metadata. • Support document authoring, review, approval, issuance, periodic review, and archival. • Manage user roles, permissions, and access controls. • Perform system configuration, troubleshooting, and issue resolution. • Support audits and inspections by ensuring system compliance and documentation readiness. • Develop SOPs, work instructions, and best practices related to document management. ComplianceWire LMS Administration • Administer ComplianceWire LMS including course assignments, curricula, and training matrices. • Manage user accounts, roles, and organizational structures. • Track and report training compliance and completion metrics. • Support onboarding and role-based training programs. • Configure and maintain learning paths and certification requirements. Required Qualifications • SME-level experience administering Veeva QualityDocs (QDocs). • Strong hands-on experience with ComplianceWire LMS administration. • Experience supporting GxP-regulated environments (biotech, pharma, medical device). • Knowledge of quality systems, document control, and training compliance processes. • Experience with system configuration, workflows, and access controls. • Strong troubleshooting and problem-solving skills. • Ability to work independently in a remote, fast-paced startup environment. • Excellent communication and stakeholder management skills.