200 English-speaking jobs in Walloon Brabant

Construction Project Manager with 3-4+ years of experience managing site delivery across MEP and electrical interfaces. Strong organizational and stakeholder management skills required.

Cloud Engineer with 15+ years of experience in IT required. Expertise in containerization, network architecture, load balancing, databases, version control, monitoring tools, security practices, messaging queues, infrastructure-as-code, configuration management, and AI-powered code assistants.

Design, analyze, optimize, and test electromechanical systems and components. Collaborate with teams to deliver project outcomes. Provide technical support and report to team leaders.

Manage and optimize the international oracdecor.com website, ensuring accurate content, user experience, and SEO. Support digital marketing initiatives and collaborate with teams to align on content needs. Analyze website performance and implement improvements.

Become one of 10 Future Shapers in this 18-month program starting October 1, 2026. You'll gain experience in digitalization, AI, smart infrastructures, and energy efficiency through three 6-month rotations. The program includes project management, finance, safety, and language training.

The Quality Control Release & Stability Testing Director leads end-to-end oversight of QC release and stability testing activities for clinical products. This role defines strategy, builds and leads teams, drives technical and regulatory excellence, and partners across functions to ensure timely, compliant product release and a robust stability program. Responsibilities include method lifecycle management, KPI development and reporting, SOP authoring, investigation guidance, team leadership, operational management of sample receipt, testing, and data review, and ensuring compliance with GMP and regulatory requirements.

This internship focuses on end-to-end logistics and supply chain transformation. The intern will contribute to designing a new operating model, evaluating potential solutions, and improving existing supply chain processes. The role requires a Master's student in Supply Chain or a related field, fluency in English, and the ability to work both remotely and on-site.

As a Delegate Qualified Person, you will ensure compliance with EU and Belgian regulatory requirements and GMP/GDP standards. Responsibilities include QP certification, batch release, and oversight of quality systems. You will collaborate with global quality units, regulatory affairs, and external partners.

Associate Director will lead a team focused on decision science for clinical operations.

Senior Quality Lead to support GCP-focused vendor qualification, lead Quality Agreement lifecycle management, and contribute to risk-based oversight for a network of clinical vendors. Ensures inspection readiness and compliance with international regulations. Minimum 10 years of relevant GCP Quality experience required.

Leads a team of Study Delivery Leads in executing Non-Interventional Studies (NIS) within a designated therapy area. Collaborates with functional leaders to ensure successful study delivery, including timelines, quality, and budget. Oversees TA resource allocation, hiring, performance management, and team development. Ensures compliance with applicable regulations and GSK SOPs.

Lead the launch and growth of a new SportsMed division in Belgium. Define business strategy, manage P&L, and build relationships with key opinion leaders.

Research Assistant to support data analysis and knowledge mobilization. Requires undergraduate qualification, data entry/database management experience, website experience (WordPress), research experience with data analysis software, and advanced computer skills (Word, Excel, statistical software).

Postdoctoral Research Associate to conduct in vivo assays, develop analytical assays, and possess a PhD in a relevant discipline such as pharmacy, medicine, or pharmaceutical science.

Senior Quality Lead to support GCP-focused vendor qualification, lead Quality Agreement lifecycle management, and contribute to risk-based oversight for a network of clinical vendors. Ensures inspection readiness and compliance with international regulations. Requires 10+ years of relevant GCP Quality experience.

The Director of Europe Regulatory Policy develops and maintains regulatory policy, advocacy, and intelligence priorities for GSK's medicines portfolio in Europe. This role provides expert interpretation and advice on new legislation and policies, builds relationships with stakeholders, and collaborates with internal teams to execute regulatory strategies.

Designs, implements, and maintains network architectures for large organizations. Configures, troubleshoots, and optimizes network hardware and software. Leads small teams and possesses strong analytical and problem-solving skills. Requires at least 3 years of experience and a Bachelor's degree or equivalent experience.

Senior Quality Lead to support GCP-focused vendor qualification, lead Quality Agreement lifecycle management, and contribute to risk-based oversight for a network of clinical vendors. Ensures inspection readiness and compliance with international regulations. Requires 10+ years of relevant GCP Quality experience.

Execute validation activities for computerized systems, process equipment, and laboratory instruments in a pharmaceutical environment. Ensure compliance with US regulations and GMP systems. Collaborate with manufacturing, IT, and laboratory teams.

Senior Scientist to design, optimize, and support manufacturing processes for injectable drug products from early clinical phases through regulatory approval. Experience in sterile liquid drug product development or manufacturing required.