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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.

13
Jobs found

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

QA Specialist

Life Sciences
QA
Master
Medior (3+)

Our client, a fast-growing MedTech start-up specializing in surgical software, is seeking a professional to lead their quality initiatives. This role focuses on building a robust quality management system from the ground up and preparing for upcoming regulatory submissions.

Antwerp, Antwerp
Consultancy
Fulltime, Hybrid
Apply now

QA Operational Readiness Officer

Life Sciences
QA
Bachelor, Master
Medior (3+)

Our client, a leading pharmaceutical organization, is seeking a QA Operational Readiness Officer 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

Project Engineer Validation (Data integrity)

Life Sciences
Validation and Qualification
Master
Medior (3+)

Our client, a leading pharmaceutical organization, is seeking a Data Integrity Project Engineer to support specialized compliance projects. This role focuses on upgrading production equipment to meet GMP standards and conducting Alcoa Assessments on various systems. The position requires a hands-on approach to validation and cross-departmental coordination within a production environment.

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

QA Operational Readiness Officer

Life Sciences
QA
Bachelor, Master
Junior (0+)

Our client, a leading life sciences organization, is seeking a QA Operational Readiness Officer to support the start-up of a new production facility. The role focuses on providing comprehensive quality documentation review and hands-on operational support during the facility qualification and start-up phase.

Geel, Antwerp
Consultancy
Fulltime, Hybrid
Apply now

Cleanroom Construction Specialist

Life Sciences
Civil and Construction
Master
Senior (7+)

Our client, a leading pharmaceutical company, is seeking an expert to support the construction and revamping of classified manufacturing environments. The role focuses on overseeing the technical fit-out and internal finishes of facility upgrades to ensure operational excellence.

Geel, Antwerp
Consultancy
Fulltime, Hybrid
Apply now

Internal Operations Quality Partner

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

Microbiology Expert – Small Molecule

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

Senior Expert – GMP Certification & Pilot Plant Qualification

Life Sciences
QA
Braine-l'Alleud, Walloon Brabant
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

Production Engineer

Life Sciences
Validation and Qualification

Our client, a prominent pharmaceutical organization, is looking for a hands-on Production Engineer to provide first-line technical support. This role ensures the continuity of the production line by troubleshooting process issues and coordinating team activities within a regulated environment.

Puurs-Sint-Amands, 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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