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Jobs in Regulatory Affairs

Find your next Regulatory Affairs role in Life Sciences and help ensure compliant market access and regulatory excellence across Belgium’s leading companies.

7
Jobs found

Expert Solid State & Non-Chromatographic Analytical Technologies

Life Sciences
QA
Bachelor, Master
Advanced (5+)

Our client, a leading pharmaceutical organization, is seeking an expert to provide comprehensive oversight of non-chromatographic quality control laboratories. This role involves driving analytical excellence, ensuring regulatory compliance for small molecule APIs, and leading strategic improvement initiatives within a global manufacturing environment.

Geel, Antwerp
Consultancy
Fulltime, Hybrid
Apply now

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, Antwerp
Consultancy
Fulltime, On-site
Apply now

QA Specialist (Primary Packaging)

Life Sciences
QA
Bachelor, Master
Medior (3+)

Our client, a leading pharmaceutical company, is seeking a Lifecycle Management Specialist to support their drug product packaging operations. This role focuses on managing change controls for primary packaging materials while ensuring high quality and compliance standards through technical investigations.

Beerse, Antwerp
Consultancy
Fulltime, Hybrid
Apply now

Technical Services Manager

Life Sciences
Mechanical and Utilities
Master
Expert (10+)

Onze klant is een Belgisch bedrijf binnen de farmaceutische sector en kent een indrukwekkend groeiverhaal. Vanuit hun expertise ondersteunen zij andere farmaceutische bedrijven bij de ontwikkeling en productie van geneesmiddelen. Dankzij hun hoogstaande kwaliteit, gespecialiseerde knowhow en klantgerichte aanpak hebben zij een uitstekende reputatie opgebouwd. Vandaag zijn zij uitgegroeid tot een internationaal actieve partner voor tal van toonaangevende spelers binnen de farmaceutische industrie

Onze klant wil in het kader van een naderende pensionering een Technical Services Manager aanwerven.

We zijn op zoek naar een Technical Services Manager die eindverantwoordelijk is voor alle interne technische opvolgingen en daarbij drie teams zal aansturen binnen de domeinen Maintenance, Engineering en Cleaning. Gezien het een farmaceutische omgeving betreft, is ervaring binnen een gereguleerde omgeving een must, bij voorkeur zelfs volgens GMP-standaarden.

In deze functie neem je een belangrijke leiderschapsrol op en stuur je een team van ongeveer 25 à 30 medewerkers aan, waaronder supervisors, techniekers, onderhoudsmedewerkers en engineers.

De locatie van tewerkstelling is in de buurt van Willebroek en Mechelen.  Deze functie rapporteert aan de COO.

Antwerp
Permanent
Fulltime, Hybrid
Apply now

Utilities Project Engineer - HVAC

Life Sciences
Mechanical and Utilities
Master
Advanced (5+)

Our client, a leading pharmaceutical organization, is seeking a Utilities Project Engineer with expertise in HVAC to support infrastructure and utilities projects within existing facilities. This role focuses on managing and executing technical utilities projects while ensuring reliability and compliance in a regulated environment.

Beerse, Antwerp
Consultancy
Fulltime, Hybrid
Apply now

Expert Lab Systems Support Engineer – Digital Infrastructure & GxP Compliance

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

Our client, a leading organization in the pharmaceutical sector, is looking for an Expert Lab Systems Support Engineer to manage the operational stability and lifecycle of laboratory IT infrastructure. The role involves overseeing computerized systems within regulated environments to ensure performance, security, and full compliance with industry standards.

Geel, Antwerp
Consultancy
Fulltime, Hybrid
Apply now

Lab Operations Project Engineer

Life Sciences
Lab

Our client, a leading life sciences organization, is seeking a Lab Operations Project Engineer to bridge laboratory science and process improvement. The role focuses on supporting Quality Control environments by implementing new analytical methods and ensuring compliance within regulated settings. One contributes to the smooth introduction of testing approaches while resolving technical challenges in complex laboratory environments.

Antwerp, Antwerp
Consultancy
Fulltime, Hybrid
Apply now

Expertises in Regulatory Affairs

Whether you're passionate about regulatory strategy, compliance, or labeling, we offer opportunities across multiple specializations:

Regulatory Strategist – Define and drive regulatory strategy throughout the drug development lifecycle.

Regulatory Affairs Expert – Provide end-to-end regulatory support for development, submission, and post-approval activities.

Regulatory Affairs Specialist – Ensure compliance with EU and global regulations for pharmaceutical products.

Artwork & Labeling Consultant – Manage labeling processes and artwork reviews in line with regulatory guidelines.

Labeling Specialist – Oversee product information and ensure accurate, compliant labeling across markets.

CMC Regulatory Affairs Consultant – Support regulatory submissions related to Chemistry, Manufacturing & Controls (CMC).

Regulatory Project Coordinator – Coordinate timelines, submissions, and stakeholder communication in regulatory projects.

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