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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.
Our client, a leading manufacturer of pharmaceutical production equipment, is seeking validation professionals to support their automated systems. The project focuses on testing complex machinery on both physical and simulated platforms within a strictly regulated environment.
Our client, a global biotechnology organization, is seeking a professional to support their digital technology compliance team with computer systems lifecycle management and IT quality processes. The role involves ensuring the integrity and compliance of computerized systems within a highly regulated environment.
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 biotechnology organization, is seeking an experienced professional to manage quality investigations and process improvements. This role is responsible for driving excellence in compliance and manufacturing within a highly regulated environment.
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 global healthcare organization, is seeking a specialist to manage logistics quality compliance and deviation management. The role focuses on driving the full lifecycle of non-conformances and root cause investigations to ensure operational excellence within a regulated supply chain 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 life sciences organization, is seeking a Validation Consultant to support their digital technology compliance team. The project focuses on managing the lifecycle of computer systems and supporting IT quality processes within research and development environments.
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.
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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