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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 pharmaceutical organization, is looking for a specialist to provide data stewardship and process ownership for its regulated content and regulatory information. This role focuses on supporting end-users and managing diverse product portfolios through effective database management and training.
Our client, a leading pharmaceutical manufacturing organization, is seeking a process owner for their site-wide quality systems. This role focuses on driving compliance and continuous improvement for validation processes while serving as a subject matter expert during regulatory inspections.
Our client, a leading pharmaceutical organization, is looking for a Quality SME to support a significant capacity expansion project at one of their sites. This role ensures that engineering processes and equipment systems comply with regulatory standards from the design phase through to operational release.
Our client, a leading organization in the pharmaceutical industry, is seeking a MES Quality Engineer to join their supply chain quality team. The role focuses on providing quality oversight and ensuring the compliant release of pharmaceutical products within a specialized production environment.
For the start-up of a new production facility we are looking for a Change control coordinator/Quality operational readiness officer. This critical role serves as the Change Control Coordinator while providing technical quality oversight for facility construction, modifications and utility upgrades. The position ensures seamless transition from construction phases to operational status while maintaining full GMP compliance throughout the transformation process.
We are looking for a Warehouse QA Officer who is a team player and customer oriented to join our Pharma & Injectable Quality department.
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.
Our client, a leading pharmaceutical company, is seeking a Cleaning Validation Engineer to specialize in the development and optimization of cleaning processes for production equipment. The role combines technical expertise with operational support to ensure compliance and business continuity within a regulated manufacturing environment.
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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