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Quality Document Specialist
Job in
Newark, Essex County, New Jersey, 07175, USA
Listed on 2026-06-03
Listing for:
DBV Technologies
Contract
position Listed on 2026-06-03
Job specializations:
-
Quality Assurance - QA/QC
Data Analyst
Job Description & How to Apply Below
Description:
We are seeking a Quality Document Specialist to support the Quality Systems team within a pharmaceutical/biotech environment for a 6-12 month contract. This consultant will play a key role in managing controlled documentation and training processes, ensuring compliance with GxP standards, and supporting audit readiness activities.
Location
:
Warren, New Jersey - 3 days on site & 2 days remote
Pay Rate
:$55-$70 /hr
Document Control & Veeva Vault Quality Docs
- Process controlled documents (SOPs, Work Instructions, forms) through the Veeva Vault Quality Docs workflow
- Manage document metadata and ensure accuracy and completeness
- Route documents for review and approval in accordance with established procedures
- Execute periodic document reviews under the guidance of senior QA staff
- Assign and track training within Compliance Wire
- Monitor training completion and follow up on overdue assignments
- Troubleshoot user/learner issues and provide system support
- Assist with maintaining curricula and course content
- Escalate system integration or configuration issues as needed
- Retrieve and compile document and training records for audits and inspections
- Maintain records in accordance with GxP retention requirements
- Support audit preparation and remediation activities
- Work through document and training backlogs to maintain workflow efficiency
- Support change control processes related to documentation updates
- Ensure document control queues are up-to-date and moving forward
- Associate’s or Bachelor’s degree in life sciences or a related field
- 2–4 years of experience in GxP Quality Assurance or document control within pharma/biotech
- Hands-on experience with Veeva Vault Quality Docs
- Experience with Compliance Wire or similar LMS platforms
- Familiarity with 21 CFR Parts 210, 211, and 11
- Understanding of Good Documentation Practices (GDP)
- Strong attention to detail and organizational skills
- Ability to manage multiple priorities in a fast-paced environment
- Strong communication and collaboration skills
- Curiosity:
Keep on exploring uncharted territories. Always ask “why?” and more importantly “why not?” - Courage:
Take smart risks, mentor each other to always do better & be accountable for our choices, our opinions, and our actions - Collaboration:
Teamwork and spirit. Support each other and be equally involved in the achievement of our common goals - Credibility:
Be transparent, follow through and build trust. Educate ourselves about our unique technology.
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