English-speaking jobs in Malmedy

Senior Key Account Manager/Business Development Manager to identify, develop, and win strategic accounts in the pharmaceutical and biotechnology industry. Own key accounts, drive growth, and lead complex sales cycles. Requires 8+ years of relevant commercial experience.

Director, Clinical Data Transparency, EHDS Programme Management provides strategic and operational leadership for the EHDS programme. This role defines the EHDS strategy, governance, and implementation roadmap across cross-functional teams.

Senior Manager Logistics Consulting in Life Science. Lead logistics transformation projects, designing and redesigning processes. Requires 10+ years in life sciences supply chains, expertise in warehousing/transport, and commercial engagement growth.

Data Engineer needed to support data processing and transformation in an industrial setting. Develop and maintain data pipelines using Python, Snowflake, and AWS. Requires 1–4 years of experience and a Master's degree.

Seeking a Chauffeur for the Executive Office. Duties include operating armored vehicles, security observation, route planning, and vehicle maintenance. Requires 3+ years of driving experience and a Public Trust clearance.

International group in real estate and hospitality seeks a GL Accountant to join a finance team of five. This role offers autonomy and the chance to become a key accounting reference within the Belgian group.

Business Program Manager to define transformation roadmaps for customer contact and collection. Lead initiatives using Genesys Cloud, AI, and automation to improve journeys. Requires 10+ years of senior leadership experience and proficiency in English, French, and Dutch.

Junior Software Developer to build services for healthcare interoperability, connecting Enterprise Imaging platforms with hospital systems. Responsibilities include developing, maintaining, and testing software components using Java. Requires a CS degree or equivalent experience.

Data Coordinator (Freelance) to coordinate data initiatives across teams, ensuring data quality, consistency, and governance. Requires experience in data management, knowledge of SQL/Excel, and understanding of data protection regulations.

Complaint Quality Lead drives global complaint management and regulatory compliance for biopharmaceutical products. This role defines procedural requirements, manages outsourced units, and optimizes workflows within the eQMS Veeva Source platform.

Govern and improve the global reward framework, ensuring competitiveness and equity. This role manages annual processes, maintains job architecture, and provides data-driven insights to support business strategy.

Experienced Data Protection Officer needed to manage EU and UK data protection frameworks for Ford Motor Company and Ford Credit. This role requires expert knowledge of GDPR, UK GDPR, and DPA 2018, providing guidance across a complex multinational organization.

Senior SAP Manager to lead SAP landscape evolution and operational excellence for an environmental organization. Responsibilities include managing the SAP S/4HANA roadmap, platform strategy, budgets, and vendors. Requires 8+ years in SAP management and process improvement. Must be native in Dutch.

Oversee large-scale client engagements across Benelux, ensuring successful delivery of complex programs. Manage delivery outcomes, client relationships, and commercial performance for multi-team, multi-year programs.

Senior Cost Controller to manage monthly cost control and reporting for projects. Analyze performance, identify risks, and provide financial insights to project teams. Requires a Master's degree and 5+ years of relevant experience. Fluent in Dutch and English.

Front Office Intern role at The Hoxton, Brussels. This position involves guest relations, managing arrivals/departures, handling inquiries, and supporting the Front Office Manager. Requires a minimum 3-month internship agreement.

Regulatory Counsel, Content, provides subject matter expertise on EU content regulation like the DSA and AMFD. This role interprets laws, advises on compliance programs, and manages regulator discussions to mitigate risk.

Technical Writer needed for CMC Regulatory Team, focusing on Synthetics and/or Biotherapeutics. Prepare and compile scientific documentation for drug development and global regulatory submissions. Requires relevant Ph.D. or experience.

Develop new business and strengthen customer relationships in Belgium and Luxembourg. Identify technical challenges and translate them into commercial rental solutions for industrial clients. Requires experience in Business Development or Technical Sales.

Lead global regulatory strategies for medical devices and IVDs across product development. Provide scientific and strategic guidance for approvals and market access, supporting submissions to global health authorities.