Senior QA Document Specialist Job at GQR, Boston, MA

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  • GQR
  • Boston, MA

Job Description

A leading biotech company is seeking a contract professional to support document management and Veeva platform administration within a regulated environment.

Key Responsibilities:

  • Create, revise, and manage SOPs and other regulated documents.
  • Route documents for review/approval and ensure compliance with quality standards.
  • Guide teams on documentation best practices and data governance.
  • Maintain document metadata and lifecycle tracking in Veeva.
  • Support training, process improvements, and project timelines.
  • Configure and validate Veeva per business and regulatory needs.
  • Lead change management and coordinate with Veeva Managed Services.

Qualifications:

  • Bachelor’s in life sciences, computer science, or related field; advanced degree a plus.
  • 5+ years with Veeva QMS and system administration in GxP settings.
  • Strong knowledge of CSV, SLC, and GAMP.
  • Excellent communication and organizational skills.
  • Comfortable working cross-functionally in a fast-paced environment.

Job Tags

Contract work,

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