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Find your next Regulatory Affairs role in Life Sciences and help ensure compliant market access and regulatory excellence across Belgium’s leading companies.
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.
Our client, a global pharmaceutical leader, is seeking a Microbiology Expert – Small Molecules to support clinical and lifecycle management programs. This role involves coordinating global microbiology activities and providing scientific expertise in method qualification and validation within an R&D environment.
Our client, a leading global pharmaceutical organization, is seeking an experienced QA Specialist to serve as a global Quality Representative. The role focuses on consolidating international serialization systems and defining quality requirements for a new automation integration layer across various manufacturing sites.
Our client, a leading biotechnology organization, is seeking a professional to support the start-up of a new production facility. The project focuses on technical transfers, sterilization validation, and equipment introduction to expand therapeutic manufacturing capacity. This role ensures that all manufacturing processes are developed and validated according to the highest industry standards.
Onze klant, een internationale speler in de farmaceutische sector, is op zoek naar een gedreven CSV Engineer om hun kwaliteit en- validatie team te versterken. Je komt terecht in een dynamische werkomgeving waar je de volledige verantwoordelijkheid draagt voor de validatiestatus van IT-systemen binnen een gereguleerde productieomgeving.
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.
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.
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.
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.
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.
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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