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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.

9
Jobs found

Regulatory Affairs Specialist – Biocides & Expansion Markets

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

Onze klant is een gespecialiseerde kennispartner in de provincie Limburg die internationale leveranciers begeleidt bij de registratie van biociden op de EU-markt. Je komt terecht in een klein, groeiend team waar in-house regelgevende expertise de kern vormt van de dienstverlening. Deze rol biedt de kans om volledig eigenaarschap te nemen binnen een organisatie die volop uitbreidt naar aangrenzende regelgevingskaders en internationale markten.

Limburg
Permanent
Fulltime, On-site
Apply now

Program Manager

Life Sciences
QA
Wavre, Walloon Brabant
Consultancy
Fulltime, Hybrid
Apply now

Business analyst (SAP)

Life Sciences
(Project) Management
Bachelor, Master
Advanced (5+)

Our client, a leading international organization, is seeking a candidate to support the management of its global production applications. The role involves providing business support and ensuring compliance during the transition to new technology platforms across numerous global locations.

Wavre, Walloon Brabant
Consultancy
Fulltime, Hybrid
Apply now

Microbiology Expert – Small Molecules

Life Sciences
Lab
Master, PhD
Beerse, Antwerp
Consultancy
Fulltime, Hybrid
Apply now

Automation Project Engineer - Siemens

Life Sciences
Process and Manufacturing
Medior (3+)

Our client, a leading pharmaceutical company, is seeking an Automation Project Engineer to lead specialized system upgrades. The project focuses on modernizing shopfloor systems and ensuring compliance with stringent industry regulations.

Heist-op-den-Berg, Antwerp
Consultancy
Fulltime, On-site
Apply now

Reference Standard Owner

Life Sciences
QA
Master
Junior (0+)

Our client, a leading pharmaceutical organization, is seeking a Reference Standard Owner to support a highly regulated production environment. This role involves managing the full lifecycle of assigned reference standards, ensuring all qualification and requalification activities meet stringent quality standards and project timelines.

Beerse, Antwerp
Consultancy
Fulltime, Hybrid
Apply now

Project and Validation Engineer

Life Sciences
Validation and Qualification
Bachelor
Medior (3+)

Our client, a leading pharmaceutical organization, is seeking a professional to manage small-scale engineering projects focused on filling and packaging equipment. This role involves overseeing the entire technical lifecycle of machinery, from initial commissioning through to final qualification.

Heist-op-den-Berg, Antwerp
Consultancy
Fulltime, On-site
Apply now

HSE Coordinator

Life Sciences
Civil and Construction

Our client, a prominent player in the pharmaceutical industry, is seeking a professional to manage the daily organization and monitoring of site activities. This role focuses on hands-on field supervision of contractors and ensuring the seamless integration of safety and planning within a complex project environment.

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

Global HVAC & Black Utilities Expert

Life Sciences
Mechanical and Utilities
Master
Senior (7+)

Our client, a leading global biopharmaceutical organization, is seeking a Global HVAC & Black Utilities Expert to spearhead technical strategy and standards across international manufacturing sites. The role focuses on developing engineering guidelines, leading feasibility studies for major CAPEX projects, and driving innovation within utility systems.

Braine-l'Alleud, Walloon Brabant
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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