71 English-speaking jobs in Charleroi

Sales and Relationship Specialist internship in the humanoid robot industry. Analyze market potential, build client relationships, deliver presentations, and acquire new clients in the Benelux region.

Leads end-to-end digital supply chain projects, including cold chain and warehouse technology solutions. Manages scope, timelines, budget, risks, and dependencies across stakeholders. Ensures solutions meet regulatory and cybersecurity requirements.

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.

Execute validation activities for computerized systems, process equipment, and laboratory instruments in a pharmaceutical environment. Ensure compliance with US regulations, GMP systems, and EHS requirements. Collaborate with manufacturing, IT, and laboratory teams to implement validation programs.

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, industrial follow-up, and certification compliance of aerospace components and systems. Responsibilities include participating in design and safety reviews, analyzing non-conformities, ensuring certification compliance, performing safety analyses, and preparing safety compliance documentation.

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 industry 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 will provide scientific expertise to manage physico-chemical method development activities for Biologicals Products. Responsibilities include designing experiments, managing laboratory activities, contributing to release and stability testing, and preparing documentation. Requires a Master's or Bachelor's degree in biochemistry or analytical chemistry, proven expertise in the biotech industry, and experience in analytical techniques such as chromatography or electrophoresis.

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

Senior Cybersecurity Consultant to implement EU Cyber Resilience Act (CRA) compliance for industrial products. Focus on hardening, vulnerability remediation, SBOMs, and technical documentation. Must have CRA knowledge and experience in industrial/product security.

Cybersecurity Architect needed to define and manage cybersecurity architecture for complex engineering projects. Experience in cybersecurity architecture, risk analysis, and security technologies required.

Embedded Software Engineer to design, develop, and test secure embedded software in C/C++ for military radio communication accessories. Requires proficiency in C/C++, experience with STM32 M4 MPUs, FreeRTOS, and embedded software development. Must be able to obtain a security clearance.

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.

Product Owner / Project Manager to industrialize an automated visual inspection solution for ophthalmic lens manufacturing. Responsibilities include product roadmap definition, customer project leadership, on-site deployment, and performance data analysis. Requires experience in optical inspection, regulated manufacturing, and project management.

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.

Analyze business requirements, design functional specifications, and support implementation for cloud-based SaaS solutions. Collaborate with stakeholders, architects, and development teams.

Experienced Pediatrician Specialist needed for a dynamic team providing high-quality care to infants, children, and adolescents. The role involves outpatient, inpatient, maternity, and emergency care, with responsibilities including diagnosis, treatment, and patient communication. Must have a medical degree with completed specialization in pediatrics and legal authorization to practice.