​Are you a seasoned CSV professional with PCS 7 expertise? Do you thrive in dynamic pharmaceutical environments and want to be part of a major biological bulk production project? Join us to support the BOC building expansion, a key initiative in advancing cutting-edge biomanufacturing.

Your Role

As a CSV Expert, you’ll play a critical role in:

• Leading qualification and validation activities for computerized systems in the BOC building.

• Supporting remediation work on initial installations 

• Shaping validation strategies in collaboration with project and technical teams. 

• Ensuring systems are compliant, reliable, and optimized for project success.

What We’re Looking For

• 8+ years of CSV experience in pharma or biotech.

• In-depth expertise in PCS 7 (essential).

• Solid knowledge of GMP regulations and industry best practices.

• Ability to work independently while coordinating with cross-functional teams 

• Strong communication skills in English.

Location & Conditions

Primarily on-site, with up to 60% remote flexibility based on project needs.

Position based in Belgium, ideal for candidates seeking impactful, high-visibility work in a global life sciences environment.

Why Join Us?

• Be at the forefront of innovation in biologics manufacturing.

• Work in a collaborative and expert-led environment.

• Contribute directly to a mission-critical project with long-term impact.

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 Apply now and make your expertise count where it matters most!