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Quality Document Specialist

Job in Newark, Essex County, New Jersey, 07175, USA
Listing for: DBV Technologies
Contract position
Listed on 2026-06-03
Job specializations:
  • Quality Assurance - QA/QC
    Data Analyst
Salary/Wage Range or Industry Benchmark: 55 - 70 USD Hourly USD 55.00 70.00 HOUR
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

Key Responsibilities:

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
Qualifications:
  • 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
Behavioral 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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