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Supplier Quality Specialist
BrusselsNegotiable

Quality Systems & Supplier Quality Specialist (Compliance & Remediation) Location: Brussels, Belgium (3 days onsite / 2 days remote)Contract: 12 months Overview We are seeking a proactive and detail-oriented Quality Systems & Supplier Quality Specialist to support a key compliance and remediation programme within a global medical device organisatio...

ERP Program Manager
LiegeNegotiable

ERP Program Manager Location: Liège, Belgium (remote with monthly on-site)Start Date: ASAPContract Length: 12 months (freelance)About the OpportunityA leading organisation in a highly regulated environment is seeking an experienced Program Manager to support the implementation and optimisation of Microsoft Dynamics 365 (D365 Finance & Operations). ...

C&Q Engineer
GhentNegotiable

Location: Belgium (Ghent) Contract End Date: 31 December 2026IMPORTANT REQUIREMENTS - PLEASE READ FIRSTMust be able to work on site in BelgiumMust speak Dutch and English fluentlyMust hold an EU passport or have existing EU work authorizationNo visa sponsorship or relocation sponsorship availableJob OverviewAn innovative pharmaceutical manufacturi...

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Selby Jennings Start Your Career In Recruitment
Manufacturing Technician
GhentNegotiable

Manufacturing / Maintenance Technician 6‑Month Contract | Medical Devices | Cleanroom ManufacturingLocation: Ghent, Belgium A medical device company in Ghent is seeking an experienced Manufacturing Technician to support the assembly and upkeep of high‑precision sensor components. This is a 6‑month contract role within a cleanroom manufacturing envi...

QA
BrusselsNegotiable

The role supports quality oversight of external manufacturers (CMOs) producing clinical trial products, within a highly matrixed, global environment. The position is non‑signature and does not include decision‑making authority. Job Title: QA / Clinical Quality Support ContractorContract: 1.5 years | Full‑time (40 hours/week) | Immediate start Key R...

QA
BrusselsNegotiable

The role supports quality oversight of external manufacturers (CMOs) producing clinical trial products, within a highly matrixed, global environment. The position is non‑signature and does not include decision‑making authority. Job Title: QA / Clinical Quality Support ContractorContract: 1.5 years | Full‑time (40 hours/week) | Immediate start Key R...