156 English-speaking jobs in Walloon Brabant

Leads the safe, reliable, and efficient day-to-day operation of laboratory buildings and infrastructure. Manages building changes, equipment setup, and facility improvement projects. Oversees maintenance, repairs, and technical issues with internal teams and vendors. Identifies opportunities to improve operations and user experience.

Leads a team of network engineers, delivering network projects and ensuring secure, scalable, and resilient solutions. Manages day-to-day network operations, incident resolution, and service improvements. Collaborates with stakeholders to deliver reliable connectivity across various environments. Contributes to network roadmap and long-term improvements. Requires a Bachelor's or Master's degree in a relevant field and strong experience in enterprise network design, engineering, and service delivery.

Junior Bioanalytical Scientist to develop PK bioanalytical methods, primarily LBA, supporting drug candidates in clinical development.

PhD fellowship investigating the impact of generative AI on academic editing. The project examines linguistic differences between professional and AI-generated edits and how academic writers engage with AI-assisted language editing.

Lead the consolidation and reporting function, ensuring accuracy and timeliness of group accounts under IFRS. Drive harmonization of accounting practices and optimize the consolidation system.

Senior Software Engineer needed with 5+ years of experience in programming and SQL. Proven ability to deliver high-quality software through clean code, testing, and code reviews. Must have strong technical skills, a creative mindset, and excellent algorithmic and conceptual thinking.

Leads the identification, development, and implementation of drug delivery systems from research to commercialization. Ensures delivery solutions are patient-centric and aligned with UCB product strategies. Collaborates with cross-functional teams to anticipate needs, align stakeholders, and ensure continuity.

The Vendor Quality Lead & QP provides QA expertise for Global Vendors engaged in GMP manufacturing. Responsibilities include managing vendor quality agreements, reviewing deviations and investigations, and ensuring timely completion of Product Quality Reviews. The role requires a Master's degree in a relevant scientific discipline, eight years of QA experience in the pharmaceutical sector, and a valid Qualified Person (QP) Certification. Fluent English is required.

AI Product Lead will define and deliver AI products that transform process development, manufacturing, and supply. The role requires experience shaping and delivering AI products, leading end-to-end product development, and connecting business needs with technical feasibility.

Develop, implement, and lead Pharmacometrics AI/ML strategy to support drug development. Evaluate and implement emerging technologies for quantitative clinical pharmacology and pharmacometrics applications. Perform AI/ML, population PK/PD, exposure-response modeling, and clinical trial simulations.

Designs customer-centric cryptographic architectures, analyzes security needs, and defines optimal solutions. Leads system specification, design, and Make/Team/Buy decisions, collaborating with hardware, software, security, and QA teams. Acts as the technical authority on cryptography, driving innovation, risk assessments, and best practices.

Data Analyst / SQL Specialist needed to create reports, write and review SQL queries, and analyze data across internal platforms. Must have strong SQL experience, ability to understand business needs, and attention to detail.

VIE Data Scientist specializing in chemistry to structure, analyze, and exploit historical chemical reaction data. Responsibilities include data cleaning, quality control, analysis for insights, and preparing data for integration with modern systems. Requires a Master's degree or early-stage PhD in chemistry, cheminformatics, data science, or a related field. Strong Python programming skills and experience with data handling are essential.

Principal Scientist will generate scientific insights to support product development decisions. Responsibilities include designing and interpreting experiments, exploring analytical approaches, and communicating recommendations. Requires a doctoral degree in a relevant field and 5+ years of industry experience in colloidal and granular materials characterization.

Design and maintain high quality digital solutions in electronic engineering. Experience in digital PCB design and digital electronics norms, laws, and standards required.

Provide statistical consultation on clinical trial design and analysis across multiple development stages and therapy areas. Develop and implement innovative statistical approaches, including model-based methods. Communicate complex quantitative topics clearly for diverse audiences. Contribute to scientific publications and industry initiatives.

This role contributes to the design and delivery of a biologics manufacturing facility, ensuring compliance with regulatory and quality requirements. The Qualification and Validation Lead will define and represent qualification and validation requirements, review technical documentation, and support audits and regulatory interactions.

Upstream Biomanufacturing Process Expert needed for biologics manufacturing facility design and delivery. Expertise in cell culture, bioreactor operations, and media preparation required. Collaborate with global teams and technical experts to ensure efficient, scalable production. Bachelor's degree in biotechnology, bioprocess engineering, or related field required. Proven experience in biologics manufacturing and regulated environments. Fluent in English. Occasional travel to the United States may be required.

Downstream Biomanufacturing Process Expert needed for a biologics manufacturing project. Will represent manufacturing needs, translate operational requirements, and ensure the future facility is designed for safe, high-quality, and efficient production. Requires a degree in a relevant field, experience in biopharmaceutical operations, and strong knowledge of mammalian biopharmaceutical production. Fluent in English, occasional travel to the US may be required.

The Evidence Quality Lead ensures compliant Research, Development, and Pharmacovigilance processes from candidate to commercial branding. This role develops and maintains quality strategies, identifies and manages risks, and leads compliance investigations. The ideal candidate has a Bachelor's degree in a relevant field, 10+ years in the (bio)pharmaceutical industry, and experience with ATMP regulatory frameworks.