104 English-speaking jobs in Walloon Brabant

The Engineering Delivery Manager leads the technical execution of complex engineering systems, ensuring on-time, on-budget, and high-quality delivery. Responsibilities include defining the engineering delivery strategy, managing project scope and resources, and leading cross-functional teams.

Lead a key expansion area within neuroimmunology strategy, focusing on peripheral immune mechanisms influencing neurological disease. Build and lead a team, drive target identification and progression, and translate research into impactful solutions.

Supply Chain Consultant role requires strong analytical skills, preferably with a Master's degree in Production Management, Logistics, or similar. Must have basic programming skills, be fluent in English, and be willing to learn new software.

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

Contribute to regulatory bioanalysis activities supporting new therapy development. Perform routine analysis on samples and validate bioanalytical methods in a GLP-compliant environment.

Global Physical Asset Manager for biopharma equipment. Oversees lifecycle performance, ensuring safety, compliance, and efficiency. Develops asset management strategies across research, development, and manufacturing.

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

Leads and mentors a cybersecurity product engineering team, ensuring adherence to Thales' engineering standards and cybersecurity best practices. Oversees the definition, implementation, and validation of hardware/software security measures across the product lifecycle.

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.

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.

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.

Lead and manage a team of embedded software engineers, ensuring the successful delivery of high-quality, reliable, and secure embedded software. Oversee the estimation and planning of development tasks, ensuring project deadlines are met. Drive continuous improvement initiatives within the team and the broader organization.

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.

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.

Leads quality function for products, ensuring compliance with legal, regulatory, and customer requirements. Manages QA/QC procedures, inspection methods, and supplier quality. Provides quality leadership, technical expertise, and coaching to Quality teams.

Lead multidisciplinary System Architecture activities across Solution, Requirements & Verification, Interface Definition & ConOps functions. Provide technical leadership and direction to SE teams supporting complex aerospace and defense programs. Manage system architecture, interface control, requirements development, verification & validation, and technical trade studies.