Veeva QualityDocs & ComplianceWire Administrator; Consultant
Listed on 2026-01-24
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IT/Tech
IT Support, Cybersecurity, Data Analyst, Data Security
Location: New York
Veeva Quality Docs & Compliance Wire Administrator (Consultant)
Location:
Remote
Duration:
Consultant / Contract
We are seeking an experienced Veeva Administrator Consultant to support and manage our Veeva Quality Docs (QDocs) and Compliance Wire 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 Quality Docs (QDocs) and Compliance Wire LMS.
Key Responsibilities- Veeva Quality Docs (QDocs) Administration
- Serve as SME and primary administrator for Veeva Quality Docs.
- Configure and manage document life cycles, 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.
- Compliance Wire LMS Administration
- Administer Compliance Wire 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.
- SME-level experience administering Veeva Quality Docs (QDocs).
- Strong hands-on experience with Compliance Wire 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.
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