More jobs:
Quality Document Specialist
Job in
Bernards Township, Somerset County, New Jersey, 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
Overview
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
Training Management (Compliance Wire)
- 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
Audit & Inspection Readiness
- 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
Operational Support
- 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 exploring and ask questions to improve processes - Courage:
Take smart risks, mentor others, and be accountable for actions - Collaboration:
Teamwork and commitment to shared goals - Credibility:
Be transparent and build trust through follow-through
To View & Apply for jobs on this site that accept applications from your location or country, tap the button below to make a Search.
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).
Search for further Jobs Here:
×