QA Documentation Specialist I

SGS Consulting
California

Job Responsibilities:

  • Support the implementation, execution, and maintenance of the PQS integration and Quality Documents in Veeva at the Vacaville site.
  • Collaborate with the Quality Document control group to complete workflows, document gating, and coordinate elements of the document change process to ensure minimal disruption to site operations.
  • Initiate and manage documents in Veeva Quality Docs.
  • Format and edit control documents.
  • Track and log requests for source documents.
  • Ensure all activities are conducted in compliance with cGMP and global requirements.
  • Strive to maintain the highest level of inspection readiness at all times.

Skills:

  • 1-3 years of experience in Quality within the pharmaceutical or biopharmaceutical industry, preferably within a supplier quality function.
  • Ability to effectively collaborate within a diverse, cross-functional team.
  • Preferred experience with Veeva Quality Document Management System and Microsoft Teams.
  • Preferred technical writing experience.

Education/Experience:

  • On-site presence at the Vacaville location is required.
Posted 2025-11-14

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