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Jobs in Qualification & Validation

Find your next Qualification & Validation role in Life Sciences and help ensure compliant, reliable, and high-quality processes across Belgium’s leading companies.

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Validation Engineer

Validation and Qualification

Validation Engineer

Description

The Validation Engineer is responsible for the development, implementation and execution of validation activities for cGMP-critical process systems, ensuring compliance with regulatory, user and internal requirements.

This role involves hands-on validation work and the preparation and execution of validation documentation within a regulated pharmaceutical environment.

Fulltime, Hybrid

Data Integrity Specialist QA-CSV

Validation and Qualification

Our client, a leading pharmaceutical organization, is looking for a Data Integrity Specialist QA-CSV to support their supply chain systems. This role involves managing quality and compliance for diverse systems within a regulated environment, ensuring data integrity across various operational activities.

Beerse, Antwerp

Fulltime, Hybrid

CAR-T QA C&Q Engineer

Validation and Qualification

Our client, a leader in innovative pharmaceutical solutions, is seeking a CAR-T QA C&Q Engineer to join their specialized quality team. This role focuses on the review and approval of qualification activities for facilities, utilities, and process equipment within a cutting-edge manufacturing environment.

Ghent, East Flanders

Fulltime, Hybrid

Utilities Project Engineer

Validation and Qualification

Bachelor, Master

Our client is looking for a Utilities Project Engineer to support the utilities and process technology teams. This role involves managing technical projects and equipment improvements from design to handover within a complex industrial environment.

Bornem, Antwerp

Fulltime, On-site

Analist Digitalisatie Validation

Validation and Qualification

Bachelor, Master

Puurs-Sint-Amands, Antwerp

Launch Excellence Project Engineer

Validation and Qualification

Puurs-Sint-Amands, Antwerp

Fulltime, On-site

Launch Excellence Project Engineer

Validation and Qualification

Puurs-Sint-Amands, Antwerp

Fulltime, On-site

Project Engineer Site Technical Services (MDCP)

Validation and Qualification

Our client, a leading pharmaceutical organization, is seeking a technical expert to provide project-driven support for robust manufacturing operations. This role focuses on sustaining on-market medical devices and combination products through technical improvements, process changes, and risk management activities. The position acts as a bridge between production and R&D to facilitate product launches and ensure continuous improvement.

Puurs-Sint-Amands, Antwerp

Fulltime, On-site

Project Engineer I - Filling & Aseptic Processing

Validation and Qualification

Puurs-Sint-Amands, Antwerp

Fulltime, On-site

Junior CSV Engineer

Validation and Qualification

Bachelor, Master

Fulltime, On-site

Project Engineer Site Tech Services

Validation and Qualification

Puurs-Sint-Amands, Antwerp

Fulltime, On-site

(Junior) Equipment System Validation Engineer

Validation and Qualification

Bachelor, Master

Onze klant, een vooraanstaande organisatie binnen de life sciences, is op zoek naar een gedreven professional voor de documentatie en validatie van mechanische systemen en apparatuur. De focus ligt initieel op het uitvoeren van design qualifications en breidt later uit naar het uitvoeren van validatietesten zoals IOQ.

Fulltime, Hybrid

Expertises in Qualification & Validation

Whether you're passionate about process validation, computer system validation, or equipment qualification, we have opportunities across multiple specializations:

Process Validation Specialist – Validate manufacturing processes and ensure consistent product quality.

Cleaning Validation Engineer – Develop and execute cleaning validation protocols and studies.

Commissioning Manager – Lead commissioning activities for pharmaceutical facilities and equipment.

CQV Manager – Manage commissioning, qualification, and validation projects end-to-end.

CSV Consultant – Validate computer systems and ensure data integrity compliance.

Risk Assessment Specialist – Conduct risk assessments for validation and qualification activities.

Compliance Engineer – Ensure validation activities meet GMP and regulatory requirements.

Equipment Validation Specialist – Perform IQ, OQ, and PQ for manufacturing equipment.

Cleanroom Validation Specialist – Qualify and validate cleanroom environments and HVAC systems.

Computer Validation Consultant – Validate computerized systems and software applications.

Validation Coordinator – Coordinate validation projects, documentation, and timelines.

MBR Editor – Create and edit Master Batch Records for manufacturing processes.

MBR Designer – Design comprehensive Master Batch Records and production documentation.

MBR Reviewer – Review and approve Master Batch Records for accuracy and compliance.

Master Batch Specialist – Develop master batch documentation and recipes.

Validation Project Manager – Lead validation projects from planning through execution and closure.

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