418 English-speaking jobs in Walloon Brabant

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

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.

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.