176 English-speaking jobs in Walloon Brabant

Manages the Deployable CIS (DCIS) infrastructure, ensuring system readiness and availability. Supports exercises, manages security accreditation renewals, and conducts risk assessments. Develops change management plans, manages budgets, and ensures system documentation is updated. Manages contractor support, provides input to SLA reports, and supports project managers. Requires a Bachelor's degree and 5 years' experience as a Service Delivery Manager or similar role, with in-depth knowledge of business application technologies and IT service management best practices. ITIL Intermediate or Expert /Managing Professional and PRINCE 2 Foundation level or PMI PMP certifications are required.

Manages the Deployable CIS (DCIS) infrastructure as a service, ensuring system readiness and availability. Oversees engineering support, manages security accreditation renewals, and conducts risk assessments. Develops change management plans, supports budget submissions, and ensures system documentation is updated. Manages spare parts, contractor support, and provides input for SLA reports.

Systems Engineer to design, deliver, and maintain critical communication solutions for homeland and defense customers. Responsibilities include understanding customer needs, defining solutions, writing technical specifications, and contributing to testing, configuration, and troubleshooting. Requires a Master's degree in Computer Science or Telecommunications with 3+ years of experience in systems integration and/or advanced technical support. Must have demonstrable skills in at least 4 of the following: datacenter virtualization, managed network equipment, scripting, Linux/Windows servers, IP networks, VoIP, SIP, Asterisk. Fluent in English, French or Dutch is an asset.

Cefic seeks a motivated graduate for a 3-month internship in its Petrochemicals Europe department (June-September 2026). The intern will analyze industry data, provide policy recommendations, and contribute to EU policy discussions.

The Non-Clinical DMPK Outsourcing Expert oversees outsourced in vivo DMPK studies, ensuring scientific rigor, operational efficiency, and regulatory compliance. The role involves planning, coordinating, and monitoring studies conducted at CROs, serving as the primary scientific and operational contact.

Leads the development and design validation of secondary and tertiary packaging solutions across UCB's portfolio, from clinical development through commercial lifecycle management. Drives the creation of visual identity, graphic charters, and artwork deliverables, ensuring compliance and quality. Provides technical expertise to packaging sites and partners, supporting troubleshooting, capacity optimization, and technology transfer. Collaborates in a global, cross-functional environment to ensure packaging solutions are robust, scalable, compliant, and sustainable.

Provides strategic planning, specialist advice, and stakeholder relationship management support. Leads and coordinates strategic initiatives, manages meetings, and handles confidential information. Requires a NATO SECRET security clearance and a Bachelor's degree or equivalent experience.

Designs, develops, and improves GxP learning solutions for colleagues. Translates Quality Management System processes and GxP topics into engaging, measurable learning experiences. Collaborates with stakeholders and SMEs to ensure solutions align with quality standards, SOPs, and regulatory expectations.

Designs and develops digital circuits for HF tactical products, including cryptography, radio, power control, and signal processing. Responsibilities include analysis of customer specifications, sub-system and detailed design, PCB schematics, prototype validation, and design integration. Collaborates with a multi-disciplinary team.

Ensures compliance with evolving laws and regulations for UCB compounds globally. Supports stakeholders in investigating significant events and promotes quality by design practices. Leads cross-functional quality improvement initiatives and collaborates with internal and external partners.

The R&D and PV Quality Project Lead will lead and support strategic initiatives and projects to achieve R&D and Pharmacovigilance Quality objectives. The role will translate strategy into actionable projects, manage project execution, and ensure alignment with quality and compliance standards. The Project Lead will collaborate with R&D and PV Quality teams, Regulatory Intelligence Network (RIN), and stakeholders to drive project success.

Provides operational and analytical support to Contract Manufacturing Organizations (CMOs) across the lifecycle of UCB products. Collaborates with internal and external teams to ensure compliance, efficiency, and quality in analytical processes.

The Oncology Pipeline MSL is a field-based role connecting GSK to the healthcare community. This non-promotional position focuses on advancing clinical practice to improve patient outcomes. The MSL engages with healthcare providers and account personnel to ensure understanding of GSK medicines, their benefit/risk profile, and the evolving treatment landscape. Responsibilities include identifying and engaging with healthcare professionals, contributing to medical strategy by collecting and communicating medical insights, and supporting clinical trials.

Frontend Intern will work with the development team to evolve the platform. Tasks include developing frontend features, participating in bug fixing, and contributing to code refactoring. The ideal candidate is a web development student with knowledge of HTML, CSS, JavaScript, and a component-oriented framework.

Provides global Quality oversight for Network Governance across Patient Supply Third-Party partners, Inspection Readiness, and Regulatory Intelligence. Ensures Third-Party lifecycle management, governance decisions, and inspection-related activities meet UCB quality standards. Leads Quality oversight for Network Governance and embeds Quality across Third-Party lifecycle processes. Manages and coaches the Inspection Readiness Quality Support function. Represents Quality in governance bodies and escalates risks impacting compliance or supply.

Lead a team of Pharmacometricians, applying pharmacometrics to pediatric drug development, Neurology, and Immunology. Develop and deliver pharmacometrics strategies, perform modeling, and lead project teams. Requires a PhD in a related field and 8+ years of industry experience with 2+ years of line management.

Leads a team of Biosampling Project Leaders, driving Human Biological Sample (HBS) and laboratory strategy for vaccines, GH, and ID therapeutic programs. Accountable for operational excellence, resource alignment, and compliance with regulatory and scientific standards. Requires Vaccines, GH, or ID area scientific knowledge, strong leadership, and collaboration skills.

Industrial Designer to develop machinery and module concepts, create 3D models, and ensure ergonomic, usable, and safe designs. Collaborate with engineers and product managers to translate functional requirements into manufacturable designs.

Associate Director will lead the content approval process for vaccines within GSK.

The Student Funding Officer will communicate with enquirers, process applications, and provide information. The role requires proficiency in Microsoft Office Suite, strong communication skills, and the ability to work independently and meet deadlines.