Posted:
June 03, 2026
Location:
Belgium, Belgium, Belgium

Job Description

Job description



Mission
Join our client’s Site Validation team to keep biological drug-substance operations compliant while an internal role is back-filled. After September, continued involvement is likely given the strong project pipeline.



Key Responsibilities



  • Execute routine qualification & validation protocols for small-scale equipment

  • Adapt process parameters and recipes under GMP

  • Perform non-CSV validations: building, drug-substance production equipment, periodic reviews

  • Contribute to ad-hoc project work as integration and skills allow



Must-Have


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Job Overview

Job Type: Full-time
Location: Belgium, Belgium
Posted: June 03, 2026
Deadline: July 13, 2026