Support GxP document control and learning systems at Fusion Pharmaceuticals in Hamilton, Ontario, working onsite five days each week.

This entry-level Quality position supports controlled documents and training administration for radio conjugate pharmaceutical quality systems. You will manage document workflows, learning assignments, and training records. The work applies GDP, ALCOA+ data integrity, and relevant GxP regulations.

Key Responsibilities:

- Process document revisions, reviews, releases, and retirements in eDMS
- Check formatting, references, hyperlinks, metadata, and document versioning
- Link documentation changes with change controls, deviations, and CAPAs
- Maintain compliant archives and complete scanning and filing activities
- Retrieve records for audits,



inspections, and management reporting

Requirements:

- Bachelor’s degree in a relevant scientific, technical, or business field
- Two to five years of relevant experience, including regulated projects
- Exposure to GMP, GCP, GLP, or GVP environments
- Familiarity with eDMS, LMS, QMS, or validated systems
- Ability to manage requests, deadlines, records, standing, and lifting

Bring meticulous document control, data integrity, and GxP administration skills to Fusion Pharmaceuticals’ Hamilton Quality organization.

📌 GxP Document Control Specialist Hamilton (Canada)
🏢 AstraZeneca
📍 Canada