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On Site Manufacturing Jobs in Belgium

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Manager Program Management
Brussels$180,000 USD a year

Manager, Program ManagementLocation: Madison, WI Work Model: 100% Onsite Compensation: Competitive base salary + bonus potential + comprehensive benefitsAbout the OpportunityAn expanding biologics CDMO is seeking a Manager of Program Management to lead complex client programs across biologics development and manufacturing. This individual will over...

Asset CQV Engineer
GhentNegotiable

Asset Engineer (CQV) - Ghent, Belgium (Fully Onsite)OverviewWe are seeking an experienced Asset Engineer (Commissioning, Qualification & Validation) to join a leading pharmaceutical manufacturing facility in Ghent, Belgium. This position is responsible for ensuring manufacturing equipment, utilities, and systems remain qualified, compliant, and in ...

QA-CSV Specialist & Site Key User
BeerseNegotiable

QA-CSV Specialist & Checklyst Manager Site Key UserLocation: Belgium (On-Site) Contract End Date: 31 December 2026 / 2027 ( there is one role ending 2026 and one ending 2027) Function: Quality / Validation Industry: Pharmaceutical ManufacturingAbout the RoleWe are seeking a QA-CSV Specialist & Checklyst Manager Site Key User to support a leading p...

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Process Validation
BrusselsNegotiable

Process Validation Engineer - Cell Therapy / CAR-TLocation: Ghent, BelgiumContract: Until December 2027Working Pattern: Full-time, on-siteHours: 40 hours per weekRole OverviewWe are looking for experienced Process Validation Engineers to support the start-up and implementation of an advanced cell therapy / CAR-T manufacturing operation in Ghent.Wor...

Project Manager
GhentNegotiable

We are seeking an experienced Senior Project Manager to join a leading pharmaceutical manufacturing organisation operating within a cutting-edge CAR-T and cell therapy environment. This position sits within the Engineering & Automation function and offers the opportunity to lead high-impact projects supporting critical manufacturing assets and pro...

Process Engineer Visual Inspection
KasterleeNegotiable

We are seeking an experienced Process Engineer VI to support critical Visual Inspection (VI) and Container Closure Integrity Testing (CCIT) initiatives within a GMP-regulated pharmaceutical manufacturing environment. This position will play a key role in the implementation, qualification, optimization, and lifecycle management of advanced inspectio...