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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.

6
beschikbare vacatures

Sterility Assurance Manager

Life Sciences
Validation and Qualification
Senior (7+)

Our client, a leading pharmaceutical organization, is seeking a Sterility Assurance Manager. This role focuses on developing and overseeing the sterility assurance program to maintain safety and regulatory compliance in vaccine production. The position serves as a technical expert in microbiology and aseptic processes to drive continuous improvement across manufacturing units.

Waver, Waals-Brabant
Consultancy
Fulltime, Hybrid
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Cleaning Validation Engineer

Life Sciences
Validation and Qualification
Master
Medior (3+)

Our client, a leading pharmaceutical company, is seeking a Cleaning Validation Engineer to specialize in the development and optimization of cleaning processes for production equipment. The role combines technical expertise with operational support to ensure compliance and business continuity within a regulated manufacturing environment.

Heist-op-den-Berg, Antwerpen
Consultancy
Fulltime, Hybrid
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Commissioning Lead

Life Sciences
Validation and Qualification
Bachelor, Master
Expert (10+)

Our client, a leading pharmaceutical company, is looking for a Commissioning Lead to drive the execution of an ambitious project. This role involves overseeing the entire commissioning lifecycle, bridging the gap between engineering, contractors, and quality departments to ensure successful delivery of critical installations.

Geel, Antwerpen
Consultancy
Fulltime, Hybrid
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CSV Validation Engineer

Life Sciences
Validation and Qualification
Master
Medior (3+)

Our client, a leading pharmaceutical company, is seeking a CSV Validation Engineer to join their team. This role focuses on the validation of software packages and computerized systems to ensure compliance with global regulatory standards.

Geel, Antwerpen
Consultancy
Fulltime, On-site
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Computer System Validation Engineer

Life Sciences
Validation and Qualification
Master
Medior (3+)

Onze klant, een vooraanstaande organisatie in de life sciences, zoekt een professional ter ondersteuning van Computer System Validation (CSV) activiteiten. De rol richt zich op het waarborgen dat geautomatiseerde systemen en interfaces binnen GxP-gereguleerde omgevingen voldoen aan alle regelgevende vereisten en kwaliteitsnormen.

Geel, Antwerpen
Consultancy
Fulltime, On-site
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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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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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