394 English-speaking jobs in Walloon Brabant

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.

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.

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.

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.

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.

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.

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.

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.

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.

Part-time Quality Assurance Consultant to support growing biotech operations. Responsibilities include data management, information consolidation, supplier coordination, and Quality Agreement preparation. Requires 2+ years of relevant experience, strong communication skills, and a good command of English.

Experienced MSAT Quality Lead to support technology transfers, process validation, and quality troubleshooting for pharmaceutical projects. Strong GMP knowledge and proven experience in technology transfer, investigations, and CAPA lifecycle required.

Software Architect for the Beam component within the Proton-Therapy Business Unit. Define and maintain a robust, scalable software architecture. Contribute to solution phases, analyze problems, and identify technical risks. Support and coach developers, validate design choices, and ensure architectural coherence.

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.

Bioanalytical Scientific Manager will design and execute bioanalytical strategies for biologics, small molecule, and gene therapy programs. Collaborate with cross-functional teams to translate study goals into analytical strategies and oversee bioanalytical activities.

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.

Senior Power BI Consultant will configure, tune, and optimize Power BI Server. Responsibilities include providing Level 2/3 support, managing incident and change processes, and designing and delivering Power BI dashboards. Requires a Bachelor's degree and at least 5 years of experience as a consultant on large-scale business application implementations. Minimum 5 years of experience with MS SQL Server, minimum 3 years with Power BI Report Server and Power BI Service, and minimum 3 years of Power BI development experience are required.