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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.

32
Jobs found

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

QC Analyst (Analytical & Microbiology)

Life Sciences
Lab

Our client, a leading organization in the life sciences sector, is seeking a dedicated professional to join their laboratory team. The role involves performing and evaluating complex analytical and microbiological tests within a strictly regulated quality control environment.

Antwerp, Antwerp
Consultancy
Fulltime
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

Project Manager Engineering & Automation

Life Sciences
Electromechanical
Bachelor, Master
Expert (10+)

Our client, a leader in the life sciences industry, is seeking a Project Manager to support their engineering and automation department. This role focuses on overseeing process equipment projects and ensuring the successful delivery of complex technical solutions within a regulated manufacturing environment.

Ghent, East Flanders
Consultancy
Fulltime, Hybrid
Apply now

HSE Prevention Advisor & Safety Coordinator (GMP)

Life Sciences
QHSE

Our client, a leading organization in the pharmaceutical sector, is seeking a professional to support engineering and construction projects at a GMP-regulated site. This role involves taking ownership of safety aspects during the design and realization phases, ensuring both process and construction safety for diverse project scopes.

Antwerp, Antwerp
Consultancy
Fulltime
Apply now

Senior Administrative Officer

Life Sciences
Sales and Customer Service
Bachelor
Expert (10+)

Our client is seeking a professional to join their sales support team in a dynamic and customer-focused environment. This role involves combining administrative expertise with service excellence to contribute to the growth and efficiency of the project. The successful candidate will provide essential support to customers while collaborating closely with internal teams.

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

Scientist MRI

Life Sciences
Lab
Master, PhD
Medior (3+)

Our client, a leading pharmaceutical company, is seeking a motivated professional to join their advanced analytical characterization team. This laboratory-based role involves developing innovative imaging solutions for active pharmaceutical ingredients and complex drug delivery systems.

Beerse, Antwerp
Consultancy
Fulltime, On-site
Apply now

Equipment Validation Engineer

Life Sciences
Validation and Qualification

Our client, a leading pharmaceutical organization, is seeking an Equipment Validation Engineer to ensure the reliable and compliant operation of production systems. The role focuses on managing validation documentation and testing for mechanical equipment within multidisciplinary engineering and production projects.

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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