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RCI-ABBV-33128 QA Documentation Specialist (EDMS/Veeva/TrackWise/Change Control) (Pharma/Medical Device)

Rangam
Branchburg, NJ Contractor
POSTED ON 5/8/2026
AVAILABLE BEFORE 6/7/2026

6-month contract

  • Process, edit, verify and route controlled documents within the electronic document management system.
  • Documents include procedures, forms, specifications, test methods and other quality system documents.
  • This role works across multiple functions to ensure the appropriate level of document review and approval to build and maintain robust documentation.
  • Reviews and evaluates low impact changes as Change Manager in the electronic Change Management System (OneTrack).

Education and Experience

  • Bachelor’s degree and 3 years professional experience in Documentation/ Change Control or Associate’s Degree and 5 years of experience in Documentation/Change Control required.
  • 5 years of experience in pharmaceutical/Medical Device industry preferred.
  • Knowledge of computerized systems for document management, preferably Veeva. Knowledge of Good Manufacturing Practices.
  • Computer system knowledge of MS Office and TrackWise.
  • Excellent verbal and written communication skills. Ability to work with multiple priorities with minimal supervision.

Salary : $44 - $46

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