211 English-speaking jobs in Walloon Brabant

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.

The Market Access Director EMEA executes, adapts, and operationalizes the global market access & reimbursement strategy across EMEA healthcare systems. The role owns regional access outcomes, including payer, HTA & physician engagement, translating global strategy into country-level coverage, reimbursement, and stakeholder alignment.

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.

Project Board Coordinator will plan, coordinate, and manage Project Board meetings, consolidate project data into portfolio-level reports, and prepare documentation to support decision-making.

This internal Research Degrees Coordinator role requires relevant vocational experience, understanding of regulatory issues, and excellent interpersonal and communication skills. The successful candidate will manage their workload, prioritize tasks, and make independent decisions.

Technical Assistant to support key client projects for the NATO Communications and Information Agency (NCIA). Responsibilities include change implementation, resource management, information management, project support, and business administration. Requires experience with ITSM, knowledge of ITIL, and proficiency in MS Project or ServiceNow. Valid National or NATO Secret security clearance is essential. Onsite work with some travel to other NATO sites.

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.

The Dev Lab Quality Ops Partner ensures the implementation and continuous improvement of a Quality Management System (QMS) for product development activities. Provides GMP and GSP oversight of development laboratories, pilot plants, and related activities across multiple international sites. Supports the "Issued Copy" process, documentation practices, and quality initiatives.

Quality Assurance professional to ensure the establishment and maintenance of an effective Quality Management System for product development. Experience in GMP oversight, regulatory compliance, and quality improvement within the biopharmaceutical industry is required.

Quality Assurance professional to ensure the establishment and maintenance of an effective Quality Management System for product development. Provides support for the "issued copy" process, coordinates local instructions, and supports regulatory inspections. Requires a Master's or Bachelor's degree in a relevant field and minimum 3 years of experience in Quality Assurance within the biopharmaceutical industry.

Senior Quality role acting as the primary QA point of contact for a portfolio of customers. Secure projects from a quality standpoint across the product lifecycle while building trusted customer relationships.

Develop and validate analytical methods, primarily using liquid chromatography, from early-stage development through validation and lifecycle support.

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.

Develop business software solutions for the consumer goods industry. Requires 5-10 years of commercial experience in business software or supply chain consultancy. Excellent communication skills in English are essential.

Java Developer to contribute to core platform development, perform performance testing, and analyze/fix system bottlenecks.

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.

Develop and industrialize innovative chocolate products, balancing creativity, consumer expectations, quality, and industrial constraints.