184 English-speaking jobs in Walloon Brabant

Provides business support for AMIS Identity Cards, including hardware, peripherals, and stock management. Supports Identity Management solutions. Requires 10+ years of experience in a national military, NATO HQ, or similar organization with a minimum of one year in a management role. Must have experience with large-scale identity card management systems and data protection strategies.

Leads global chemical compliance efforts for UCB's product portfolio, ensuring adherence to REACH, CLP/GHS, and other regulations. Manages chemical data submissions, supports audits and training, and collaborates with suppliers and internal teams.

The Global Quality Auditing Business Ops Lead Due Diligence ensures effective coordination and execution of quality processes for UCB Business Development initiatives. This role serves as the central QA point of contact for due diligence activities, including divestments, partnerships, acquisitions, and in-/out-licensing.

Supports GSK's recruitment efforts in Belgium by developing and implementing strategies to attract top talent. Manages the full recruitment cycle and partners with hiring managers and external partners. Requires a Bachelor's degree and 5+ years of recruitment experience.

Leads and oversees the Global Medical Information and Content Approval Team for Vaccines, ensuring promotional and non-promotional content meets quality, scientific accuracy, and compliance standards. Manages team performance, provides mentorship, and collaborates with stakeholders to align content with medical strategy and customer needs.

As Technical Product Manager, you will drive the development of product handling systems (PHS) including conveyors and automation. You will define product strategy, translate needs into technical specifications, and lead cross-functional programs. You will also manage supplier relationships, identify IP opportunities, and support marketing with program updates.

Senior Project Manager to lead strategic initiatives in logistics, data analytics, and digital transformation for a pharmaceutical partner near Brussels. Will coordinate stakeholders, technical teams, and data experts to deliver high-impact projects. Requires a Master's degree or equivalent experience in a related field and 7+ years of project management experience in pharma, supply chain, or data environments.

As Sustainability and Safety Analyst, you will support the Sustainability Director and Health and Safety Director Europe, developing and implementing sustainability strategies and promoting Carmeuse's interests. You will also contribute to the development and deployment of lifesaving procedures and support the safety policy.

Leads global engineering strategy and execution for Life Sciences software portfolio. Defines and owns long-term engineering strategy, ensuring scalable, secure, and high-quality solutions. Manages a 25-person engineering organization, fostering a culture of technical excellence and continuous improvement. Partners with Product Management, Sales, Marketing, and Professional Services to align technical strategy with business goals. Drives architectural decisions, manages third-party integrations, and ensures predictable, high-quality delivery.

Leads discovery strategy for novel lentiviral vectors (LVVs), drives engineering from concept to preclinical candidate selection, and builds screening platforms to characterize potency and safety. Manages budgets, resources, and timelines across programs/platforms. Requires PhD in a relevant field and 8+ years (Associate Director) or 12+ years (Director) of experience in gene therapy R&D focused on viral vector engineering.

Junior Group Sustainability Analyst (VIE) will report to the Group Head of Sustainability and contribute to executing the Group Sustainability Strategy. Responsibilities include setting up projects, tracking performance, providing updates to stakeholders, and supporting regional sustainability teams with data analysis.

Electronics Engineer to design, develop, and maintain embedded systems and digital logic projects. Experience with FPGA and CPLD development (VHDL/Verilog) and digital/analog electronics required.

Experienced Area Sales Manager needed for Particle Measuring Systems. Full sales cycle ownership for pharmaceutical industry products and services in the BeNeLux area.

The Principal Solutions Engineer leads the design and development of complex solution architectures for NATO, ensuring alignment with organizational requirements and standards. This role drives requirements management, systems development, and network design activities across multiple projects and initiatives.

Execute, implement, and analyze in vivo experiments to support preclinical drug development. Analyze and interpret experimental data, collaborate with interdisciplinary teams, and prioritize in vivo studies.

The IVVQ Manager leads testing activities for projects, defining the testing strategy, managing planning and performance, and guaranteeing solution quality. The role involves collaborating with engineering teams, subcontractors, and customers to drive testing development, track progress, and manage risks.

Quality Assurance Manager ensures product quality and compliance through risk management, audits, and adherence to global regulations. Leads key QA processes, including Audit Management and Risk Management. Requires 8+ years experience in Quality Management, ISO certifications, and knowledge of medical device regulations.

Lead visual merchandising strategy for Levi's® across Europe, shaping in-store experiences and driving brand consistency.

As the technical anchor of our security organization, you will lead the technical implementation of NIS2 requirements, manage security operations, and provide security architecture support. You will translate regulatory requirements into technical controls, oversee our external SOC partner, and ensure security is embedded in the development lifecycle.

This role provides leadership and Quality Assurance (QA) expertise to drive strategic and operational QA activities for vendors engaged in preclinical, clinical, and post-marketing pharmacovigilance activities. The Vendor Quality Lead ensures inspection readiness, robust contractual language, risk-based oversight, and sustainable vendor performance.