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Vacatures in Qualification & Validation

Vind je volgende functie in Qualification & Validation binnen Life Sciences en help conforme, betrouwbare en kwalitatieve processen te garanderen bij de toonaangevende bedrijven in België.

14
beschikbare vacatures

Validation Engineer

Life Sciences
Validation and Qualification
Medior (3+)

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.

Geel, Antwerpen
Consultancy
Fulltime, Hybrid
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Data Integrity Specialist QA-CSV

Life Sciences
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, Antwerpen
Consultancy
Fulltime, Hybrid
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CAR-T QA C&Q Engineer

Life Sciences
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.

Gent, Oost-Vlaanderen
Consultancy
Fulltime, Hybrid
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Utilities Project Engineer

Life Sciences
Validation and Qualification
Bachelor, Master
Junior (0+)

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, Antwerpen
Consultancy
Fulltime, On-site
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Analist Digitalisatie Validation

Life Sciences
Validation and Qualification
Bachelor, Master
Junior (0+)
Puurs-Sint-Amands, Antwerpen
Consultancy
Fulltime
Solliciteer nu

Launch Excellence Project Engineer

Life Sciences
Validation and Qualification
Master
Medior (3+)
Puurs-Sint-Amands, Antwerpen
Consultancy
Fulltime, On-site
Solliciteer nu

Launch Excellence Project Engineer

Life Sciences
Validation and Qualification
Master
Medior (3+)
Puurs-Sint-Amands, Antwerpen
Consultancy
Fulltime, On-site
Solliciteer nu

Project Engineer Site Technical Services (MDCP)

Life Sciences
Validation and Qualification
Master
Advanced (5+)

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, Antwerpen
Consultancy
Fulltime, On-site
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Project Engineer I - Filling & Aseptic Processing

Life Sciences
Validation and Qualification
Master
Junior (0+)
Puurs-Sint-Amands, Antwerpen
Consultancy
Fulltime, On-site
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Junior CSV Engineer

Life Sciences
Validation and Qualification
Bachelor, Master
Junior (0+)
Geel, Antwerpen
Consultancy
Fulltime, On-site
Solliciteer nu

Project Engineer Site Tech Services

Life Sciences
Validation and Qualification
Master, NA
Junior (0+)
Puurs-Sint-Amands, Antwerpen
Consultancy
Fulltime, On-site
Solliciteer nu

(Junior) Equipment System Validation Engineer

Life Sciences
Validation and Qualification
Bachelor, Master
Junior (0+)

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.

Geel, Antwerpen
Consultancy
Fulltime, Hybrid
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Expertises in Qualification & Validation

Of je nu gepassioneerd bent door procesvalidatie, computer system validation of apparatuurkwalificatie, wij bieden mogelijkheden in diverse specialisaties:

Process Validation Specialist – Valideer productieprocessen en zorg voor consistente productkwaliteit.

Cleaning Validation Engineer – Ontwikkel en voer reinigingsvalidatieprotocollen en -studies uit.

Commissioning Manager – Leid commissioning-activiteiten voor farmaceutische faciliteiten en apparatuur.

CQV Manager – Beheer commissioning, qualification en validation projecten van A tot Z.

CSV Consultant – Valideer computersystemen en zorg voor data-integriteitscompliance.

Risk Assessment Specialist – Voer risicobeoordelingen uit voor validatie- en kwalificatieactiviteiten.

Compliance Engineer – Zorg dat validatieactiviteiten aan GMP en regelgevende vereisten voldoen.

Equipment Validation Specialist – Voer IQ, OQ en PQ uit voor productieapparatuur.

Cleanroom Validation Specialist – Kwalificeer en valideer cleanroom-omgevingen en HVAC-systemen.

Computer Validation Consultant – Valideer geautomatiseerde systemen en softwaretoepassingen.

Validation Coordinator – Coördineer validatieprojecten, documentatie en tijdlijnen.

MBR Editor – Creëer en bewerk Master Batch Records voor productieprocessen.

MBR Designer – Ontwerp uitgebreide Master Batch Records en productiedocumentatie.

MBR Reviewer – Beoordeel en keur Master Batch Records goed op nauwkeurigheid en compliance.

Master Batch Specialist – Ontwikkel master batch-documentatie en recepturen.

Validation Project Manager – Leid validatieprojecten van planning tot uitvoering en afsluiting.

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