52 English-speaking jobs in Charleroi

Data Center Technician to support day-to-day operations. Install, rack, and cable servers and network equipment. Perform basic hardware troubleshooting and replacement. Assist with setup, maintenance, and removal of IT equipment. Follow procedures for work requests, changes, and safety standards.

Deutsche Windtechnik seeks an experienced Country Manager to lead onshore business operations in the Netherlands and Belgium. This role involves strategic oversight, operational excellence, and stakeholder management across both markets.

Experienced IT project manager to lead infrastructure, information systems security, and management projects. Responsibilities include managing project portfolios, coordinating technical teams, and ensuring project deliverables meet quality, scheduling, and governance requirements.

Finance Manager needed to shape the development and professionalization of the finance organization at Lantmännen Unibake Benelux.

As a RAMS Engineer, you will conduct safety assessments, perform RAMS analyses (FMEA, FTA), and apply safety assurance methods to traction systems and RSC safety in Charleroi. You will collaborate with project teams to ensure compliance with CENELEC standards.

Leads Certification and Validation activities for Traction level during project execution. Manages Certification and Validation QCD objectives and Traction Test Team performance. Responsible for implementing standard processes and tools to ensure efficiency. Requires experience in team and project management, traction system knowledge, and knowledge of standards and regulations.

Provide on-site support for product safety engineering activities related to the design, review, and certification compliance of aerospace components and systems. Responsibilities include conducting safety analyses, identifying failure scenarios, and ensuring compliance with aeronautical standards.

The ATC System Designer develops ATC system architecture, trackside and trainborne, defining requirements, evaluating design trade-offs, and coordinating with verification and validation activities.

Analytical Development Analyst develops, validates, and transfers physico-chemical methods for pharmaceutical products. Requires a Master's or Bachelor's degree in biochemistry or analytical chemistry, 5+ years of experience, and expertise in analytical techniques like chromatography or electrophoresis.

Automation Engineer needed for R&D team in radiopharmaceutical sector. Develop and maintain PLC software using Siemens TIA Portal. Support system upgrades and on-site deployments. Minimum 2-3 years of industrial automation experience required.

Development Analyst provides scientific expertise for managing physico-chemical method development activities for Biologicals Products. Designs experiments, manages laboratory activities, contributes to release and stability testing, and prepares documentation. Requires a Master's or Bachelor's degree in biochemistry or analytical chemistry and proven expertise in analytical method development and validation.

Manage project documentation within a dynamic environment. Implement and manage the Electronic Documentation Management System (EDMS), create/update templates, and support users.

The Clinical Project Manager delivers clinical trials on time, within budget, and to the highest quality. Responsibilities include managing timelines, budgets, feasibility, site selection, patient recruitment, and serving as the primary liaison for stakeholders and vendors. The role requires a BS/BA degree, minimum 4 years of biopharmaceutical industry experience, and 3 years leading global trials.

Scientist to support development of LC-MS pharmacokinetic assays for small-molecule and biologics assets. Will optimize experimental design, analyze data, and contribute to assay transfer to regulated environment. Requires BSc in biological discipline with 3+ years bioanalysis experience, including LC-MS, enzymatic digestion, and immunocapture purification.

Quality Assurance professional to ensure the establishment and maintenance of an effective Quality Management System (QMS) for product development. Provides support for the "issued copy process" and collaborates with development scientists to ensure compliance with GMP regulations.

Support the Sub-System Manager in managing the technical scope of traction/rolling stock subsystems during project execution. Collaborate with internal teams to ensure deliverables are aligned and on time. Assist in client interactions by providing clarification and feedback.

Vendor Quality Specialist supports GCP vendor qualification activities, manages Quality Agreement lifecycles, and participates in risk-based vendor oversight.

Experienced Device Documentation Expert needed for drug-device combination products, specializing in autoinjectors. Lead risk management, ensure regulatory compliance (ISO 13485, ISO 14971, ICH Q8/Q9/Q10/Q12, 21 CFR Part 4, EU MDR Article 117), and collaborate cross-functionally. Prepare and review device documentation (DHF, RMF, usability engineering, regulatory submissions). 8-10 years of experience in drug-device development, with expertise in medical device and combination product documentation. Fluent in English, French preferred.

Manages and completes assigned components on complex projects, ensuring customer needs and QCDP objectives are met. Leads component-level stakeholders, activities, and deliverables, coordinating with sub-system teams and resolving issues.

This VIE role focuses on Verification & Validation (V&V) for transport projects. The successful candidate will execute V&V activities, interface with design and testing teams, and contribute to the V&V strategy.