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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.

18
Jobs found

Senior Regulatory Affairs Specialist – Biocides & Expansion Markets

Life Sciences
Regulatory Affairs
Bachelor, Master
Advanced (5+)

Our client is a specialized knowledge partner based in the province of Limburg, guiding international suppliers through the registration of biocidal products on the EU market. You'll be joining a small, ambitious team where in-house regulatory expertise is the core of what they do and where there's real room to take ownership as the organization grows into adjacent regulatory frameworks and international markets.

Limburg
Permanent
Fulltime, On-site
Apply now

Computer System Validation (CSV) Engineer

Life Sciences
Validation and Qualification

Our client, a leading organization in the life sciences sector, is seeking a professional to support computer system validation activities. The role focuses on ensuring that computerized and automated systems in GxP-regulated environments are fit for purpose and comply with both regulatory requirements and internal standards.

Antwerp, Antwerp
Consultancy
Fulltime
Apply now

Quality Specialist Operations

Life Sciences
QA
Master
Medior (3+)

Our client, a prominent pharmaceutical organization, is seeking a Quality Specialist Operations to focus on quality oversight and project support. The role involves managing operational quality tasks and ensuring compliance within a strictly regulated production environment.

Puurs-Sint-Amands, Antwerp
Consultancy
Fulltime, On-site
Apply now

QA Coordinator

Life Sciences
QA
Bachelor, Master
Medior (3+)

Our client, a leading pharmaceutical organization, is seeking a MBR Coordinator to support the startup of a new production facility. The project focuses on ensuring quality readiness, operational excellence, and regulatory compliance during the commissioning phase. This role is essential for managing the transition to operational status through meticulous batch record oversight and GMP adherence.

Geel, Antwerp
Consultancy
Fulltime, Hybrid
Apply now

Graduate role: MBR Qualification Engineer

Life Sciences
Validation and Qualification
Master
Junior (0+)

Our client, a prominent life sciences organization, is seeking an professional to manage the qualification and testing of Master Batch Records. The role focuses on the development, writing, and execution of test protocols within a manufacturing execution system to ensure compliance with industry standards.

Ghent, East Flanders
Consultancy
Fulltime, On-site
Apply now

Process Engineer

Life Sciences
Process and Manufacturing

Our client, a leading pharmaceutical organization, is seeking a professional to focus on the development and optimization of production processes for biologic products. This role supports high-quality manufacturing operations across formulation, upstream, and downstream environments.

Antwerp, Antwerp
Consultancy
Fulltime
Apply now

QA Officer – Quality Systems & Operations

Life Sciences
QA

Our client, a leading pharmaceutical organization, is seeking a QA Officer to provide quality documentation support and operational quality assurance. This role focuses on maintaining high standards through risk assessments and documentation review while staying connected to the shop floor.

Geel, Antwerp
Consultancy
Fulltime
Apply now

Quality Project Associate

Life Sciences
QA

Onze klant, een toonaangevend farmaceutisch bedrijf, is op zoek naar een Quality Project Associate. In deze rol is men verantwoordelijk voor de kwaliteits- en productregistratieactiviteiten om de introductie van nieuwe producten te ondersteunen.

Puurs-Sint-Amands, Antwerp
Consultancy
Fulltime
Apply now

Microbiology Expert – Small Molecule

Life Sciences
QA
Master
Junior (0+)
Beerse, Antwerp
Consultancy
Fulltime, Hybrid
Apply now

Master Data Specialist

Life Sciences
QA
Bachelor
Medior (3+)

Our client, a leading organization in a regulated industry, is looking for a Data Operations & Orchestration Specialist to manage critical master data elements. This role ensures that data integrity within the project enables optimal material planning, production, and financial processes through efficient coordination and system maintenance.

Geel, Antwerp
Consultancy
Fulltime, Hybrid
Apply now

Supplier Quality Specialist

Life Sciences
QA

Onze klant, een toonaangevende organisatie in de farmaceutische sector, is op zoek naar een Supplier Quality Specialist om de kwaliteit van aangekochte materialen te waarborgen. De focus ligt op het uitvoeren van onderzoeken en het bewaken van de naleving van kwaliteits- en regulatoire standaarden binnen een gereguleerde productieomgeving.

Puurs-Sint-Amands, Antwerp
Consultancy
Fulltime, On-site
Apply now

Junior Validation Engineer

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

Our client is seeking a professional to support commissioning and qualification activities within a highly regulated environment. The role focuses on ensuring project compliance and managing periodic activities autonomously to meet technical standards.

Ghent, East Flanders
Consultancy
Fulltime, On-site
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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