411 English-speaking jobs in Walloon Brabant

Full-Stack Engineer to build and improve the Prezly platform, using React, TypeScript, PHP (Symfony), and PostgreSQL. Collaborate with product and design to ship features and improve existing product functionality.

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.

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.

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.

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 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.

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.

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.

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.

Quality Control Lead will design and deliver a future-ready biologics manufacturing facility. You will shape the Quality Control unit, ensuring compliance, inspection readiness, and sustainability. You will collaborate with cross-functional teams to embed QC needs in project design and execution.

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.

Process Automation Lead will design and deliver automation solutions for a future-ready biologics manufacturing facility. This role requires experience in industrial automation within biopharmaceutical environments and knowledge of automation systems, industrial IT, and digital manufacturing tools.

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.

Local Supply Chain and Warehousing Lead needed for a biologics manufacturing facility project. Represent manufacturing needs, define operational requirements, and champion quality, health, safety, and environmental standards. Bachelor's degree in a relevant field and experience in biopharmaceutical operations required. Fluent English, occasional US travel.

Program Manager for External Manufacturing Quality. Oversees CMO quality activities, ensuring GMP compliance, governance, and continuous improvement. Responsibilities include deviation management, CAPA support, change control, batch release, and complaint handling. Requires 5+ years GMP experience, strong knowledge of regulations, and experience in quality assurance activities.

Process Engineer to design, optimize, and improve sterile fill and finish processes in the biotech or pharmaceutical industries. Lead NPI and technical transfer for new customer projects. Develop and execute validation strategies and process risk assessments.