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QA Documentation Specialist

Fusion Life Sciences
Clinton, PA Full Time
POSTED ON 11/20/2025
AVAILABLE BEFORE 12/15/2025

Overview

We are seeking an experienced QA Documentation Specialist to join our Quality Systems team. The ideal candidate will focus on reviewing, redlining, and maintaining quality documentation to ensure compliance with regulatory standards. This role involves working closely with cross-functional teams to manage SOPs, change controls, CAPA documentation, and other quality records.

Key Responsibilities:

  • Review and redline quality documentation and SOPs
  • Maintain and manage quality records in compliance with QMS
  • Support change control and CAPA processes
  • Collaborate with teams to ensure accurate and compliant documentation

Required Skills:

  • QA documentation or quality systems experience
  • Experience with document review and redlining
  • Knowledge of regulatory standards (ISO 13485, FDA 21 CFR, GxP)
  • Strong attention to detail and organizational skills

Job Type: Contract

Pay: $ $25.00 per hour

Work Location: In person

Salary : $52,000

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