395 English-speaking jobs in Walloon Brabant

Financial Controller needed for market-leading automotive company in Puurs. Evaluates financial performance, mitigates risks, and optimizes business processes. Requires Bachelor's/Master's in Finance/Accounting/Economics, experience in finance, and advanced Excel skills.

Financial Controller needed for market-leading automotive company in Puurs. Evaluates financial performance, mitigates risks, and optimizes business processes. Requires Bachelor's/Master's in Finance/Accounting/Economics, experience in finance, and advanced Excel skills.

We are seeking experienced CNC operators, setters, and programmers for advanced manufacturing roles in Belgium. Set up and operate CNC machines, read technical drawings, and ensure precise production of custom components. Relocation assistance is available.

We are seeking experienced CNC operators, setters, and programmers for advanced manufacturing roles in Belgium. Set up and operate CNC machines, read technical drawings, and ensure precise production of custom components. Relocation assistance is available.

RF Engineer needed for a permanent position in the Wallonian region of Belgium. Design, analyze, integrate, and test RF and microwave systems for space communication technologies. Collaborate with multidisciplinary teams throughout the product lifecycle. Bachelor's degree in a related field and proven RF engineering experience required.

RF Engineer needed for a permanent position in the Wallonian region of Belgium. Design, analyze, integrate, and test RF and microwave systems for space communication technologies. Collaborate with multidisciplinary teams throughout the product lifecycle. Bachelor's degree in a related field and proven RF engineering experience required.

Penetration Tester will lead and participate in Red/Blue Team exercises, perform web, infrastructure, and application-level penetration testing, and conduct security design reviews.

Develops and coordinates stakeholder awareness and engagement campaigns for the ITM-RC1 Project. Creates communication materials, presentations, and promotional content. Supports the development of promotional videos and communication products. Coordinates meetings, prepares minutes, and tracks actions. Collaborates with internal stakeholders to ensure communication and awareness activities align with project objectives.

Leads service operations across Asia, driving operational excellence, customer satisfaction, and business performance. Develops and executes operational strategies, coaches Area Managers, and ensures alignment with global objectives.

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.

The Manufacturing Systems Quality Partner supports manufacturing activities in the Bio Pilot Plant and Gene Therapy building. This role collaborates with development scientists, CMC and operations teams, and technical services to support daily manufacturing, validation, and qualification activities. The Manufacturing Systems Quality Partner also works with QA colleagues, auditors, and senior management to manage deviations, change controls, inspections, and maintain compliance.

Ensures robust quality oversight of GxP-relevant digital systems, focusing on compliant implementation and control of computerized systems and data processes. Provides QA insight during system validation and ongoing oversight, supporting investigations and ensuring data integrity.

Junior Study Director will contribute to the design, coordination, and execution of Extractables & Leachables (E&L) studies, ensuring compliance with regulatory standards.

QA Specialist to oversee quality activities for Contract Manufacturers (CMOs), ensuring GMP compliance. Reviews deviations, CAPAs, change controls, and product market complaints. Requires a scientific degree, 5+ years in a cGMP environment, and proficiency in English, SAP, and Veeva.

QA Specialist to oversee quality activities for Contract Manufacturers (CMOs), ensuring GMP compliance. Reviews deviations, CAPAs, change controls, and product market complaints. Requires a scientific degree, 5+ years in a cGMP environment, and proficiency in English, SAP, and Veeva.

Buyer for a 6-month interim contract. Develop and execute category strategies, optimize sourcing activities, and manage contracts. Requires 3-5 years of procurement, sourcing, or category management experience, including running complex sourcing activities and commercial risk management.

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.

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.

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.

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.