389 English-speaking jobs in Walloon Brabant

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.

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.

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.

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.

As Product Manager EMEA, you will manage a portfolio of RFID solutions, including readers, scanners, and tags. You will define product requirements, collaborate with teams to ensure commercial success, and lead commercialization strategies.

As Product Manager EMEA, you will manage a portfolio of RFID solutions, including readers, scanners, and tags. You will define product requirements, collaborate with teams to ensure commercial success, and lead commercialization strategies.

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.

The LPO & GET Lead for Computer System Validation (CSV) & Data Integrity (DI) will own site-level CSV/DI processes, ensuring compliance with regulatory requirements. The role requires deep understanding of CSV/DI in a pharma manufacturing environment, including 21CFR Part 11, EU Annex 11, and GAMP guidelines.

The LPO & GET Lead for Computer System Validation (CSV) & Data Integrity (DI) will own site-level CSV/DI processes, ensuring compliance with regulatory requirements. The role requires deep understanding of CSV/DI in a pharma manufacturing environment, including 21CFR Part 11, EU Annex 11, and GAMP guidelines.

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.

Senior Business Analyst to join a squad focused on Building & Facility Services in a large-scale Agile environment. Responsibilities include business analysis, requirements gathering, testing, documentation, and change management. Must have 5+ years of experience as a Business Analyst, fluency in English, and strong Agile methodology experience.

Senior Solution Data Architect needed to define and implement data solutions, ensuring alignment with Target Enterprise Architecture. Requires 3+ years of experience as a Data Architect with strong Azure data stack expertise (Databricks, Synapse, ADF, CosmosDB, Azure SQL, Azure API Management, Azure App Services, Azure Analysis Services). Fluent English required.

Ensures robust quality oversight of GxP-relevant digital systems used in clinical activities. Focuses on compliant implementation and control of computerised systems and data processes, with emphasis on CSV and DI requirements. Collaborates with QA teams, Clinical Operations, and stakeholders to ensure systems are validated and operated according to regulatory expectations.

Financial Manager to lead finance function and contribute to strategic development. Oversee accounting, reporting, audits, tax compliance, cash flow, and risk management. Lead and develop finance team, drive process improvements and digitalization initiatives.

Financial Manager to lead finance function and contribute to strategic development. Oversee accounting, reporting, audits, tax compliance, cash flow, and risk management. Lead and develop finance team, drive process improvements and digitalization initiatives.

Financial Manager to lead finance function and contribute to strategic development. Oversee accounting, reporting, audits, tax compliance, cash flow, and risk management. Lead and develop finance team, drive process improvements and digitalization.

This role involves organizing and coordinating regulatory activities, supporting and coaching RA & QA Officers, and ensuring regulatory compliance. The successful candidate will manage information flow, provide regulatory support to customers, and contribute to the development of regulatory strategies.

Technical Service & Marketing Manager will execute tests on personal care formulations, interpret data, and collaborate with global technical teams. The role also involves identifying market trends, developing marketing strategies, and supporting sales through technical expertise and communication.

Experienced MSAT Quality Lead to support technology transfers, process validation, and quality oversight for pharmaceutical projects. Strong QA expertise, operational experience, and excellent communication skills required.