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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.

22
Jobs found

Regulatory Affairs Specialist – Biocides & Expansion Markets

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

Onze klant is een gespecialiseerde kennispartner die fungeert als de toegangspoort tot Europa voor internationale producenten van biociden en gewasbeschermingsmiddelen. In deze groeiende organisatie met een vlakke structuur krijg je de kans om een cruciale rol te spelen in de registratiestrategie en de uitbreiding naar nieuwe markten zoals veterinaire toepassingen. Je komt terecht in een team van experts waar inhoudelijke diepgang en een ondernemende aanpak de standaard zijn.

Limburg
Permanent
Fulltime, On-site
Apply now

Senior RWE Strategy Lead - Dermatology

Life Sciences
Regulatory Affairs
Master
Senior (7+)

Our client, a leading global biopharmaceutical company, is seeking a strategic leader to drive evidence generation strategies. This role focuses on designing and implementing real-world evidence and outcomes research to support product value and regulatory submissions within a specific disease area.

Braine-l'Alleud, Walloon Brabant
Consultancy
Fulltime, Hybrid
Apply now

Quality Coordinator

Life Sciences
QA
Bachelor, Master
Medior (3+)

Our client, a global pharmaceutical organization, is seeking a professional to oversee the quality management of third-party computerized systems providers. The role ensures that all external partners meet rigorous regulatory standards and internal compliance requirements through assessments and continuous performance monitoring.

Geel, Antwerp
Consultancy
Fulltime, Hybrid
Apply now

Launch Excellence Project Engineer - Validation

Life Sciences
Validation and Qualification
Master
Medior (3+)

Our client, a leading pharmaceutical company, is seeking a Project Engineer to manage validation aspects for new product introductions. The role involves ensuring regulatory compliance and successful implementation across the product lifecycle, with a specific focus on assembly and packaging processes.

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

Validation Engineer

Life Sciences
Validation and Qualification

Our client, a leading organization in the pharmaceutical and biotechnology sector, is seeking a Validation Engineer to support the validation of equipment, systems, and processes. This role ensures that facilities, utilities, and computerized systems remain compliant with regulatory and quality requirements throughout their entire lifecycle.

Antwerp, Antwerp
Consultancy
Fulltime, Hybrid
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

QA Engineer

Life Sciences
QA

QA Engineer

Pauwels Consulting — Life Sciences & Pharma, België

Over de functie

Voor een groeiende farmaceutische/biotech-organisatie in België zijn we op zoek naar een QA Engineer. Je speelt een sleutelrol in het bewaken van productkwaliteit en regelgeving binnen productie- en labprocessen, in nauwe samenwerking met Productie, QC en Regulatory Affairs.

Antwerp, Antwerp
Consultancy
Fulltime
Apply now

QA / Qualification & Validation Specialist

Life Sciences
QA
Bachelor, Master
Medior (3+)

Our client, a prominent player in the healthcare industry, is seeking a professional to join their quality team. The role focuses on overseeing compliance throughout the system lifecycle and managing qualification activities within a regulated environment.

Beerse, Antwerp
Consultancy
Fulltime, Hybrid
Apply now

QA Qualification Engineer

Life Sciences
QA
Bachelor, Master
Medior (3+)

Our client, a leading pharmaceutical organization, is seeking a QA Qualification Engineer to provide quality oversight for process and laboratory equipment. This role focuses on managing qualification activities throughout the system lifecycle to ensure strict compliance with international regulations and quality standards.

Beerse, Antwerp
Consultancy
Fulltime, Hybrid
Apply now

Launch Excellence Technician I

Life Sciences
Validation and Qualification
Bachelor
Junior (0+)

Our client, a leading pharmaceutical organization, is seeking a professional to ensure the end-to-end validation of new products across formulation, filling, and packaging. This role focuses on supporting product launches through rigorous documentation, production follow-up, and quality investigations within a dynamic project environment.

Puurs-Sint-Amands, Antwerp
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

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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