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Quality Document Specialist

Job in Bernards Township, Somerset County, New Jersey, USA
Listing for: DBV Technologies
Full Time position
Listed on 2026-07-31
Job specializations:
  • Quality Assurance - QA/QC
    QA Specialist - Analyst/Manager
Salary/Wage Range or Industry Benchmark: 114000 - 145000 USD Yearly USD 114000.00 145000.00 YEAR
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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