AdeptSource · 1 day ago
Veeva QualityDocs & ComplianceWire Administrator (Consultant)
AdeptSource is seeking an experienced Veeva Administrator Consultant to support and manage their Veeva QualityDocs and ComplianceWire LMS platforms. The consultant will act as a subject matter expert, overseeing administration, user support, document lifecycle management, and training compliance activities in a clinical-stage biotech setting.
BiotechnologyConsultingLife ScienceProfessional ServicesStaffing Agency
Responsibilities
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
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
Qualification
Required
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