50 English-speaking jobs in Wavre

You will provide tactical oversight of the end-to-end supply chain for assigned GSK R&D clinical studies, from protocol review through to study close-out and reconciliation. You will define detailed demand and supply plans for investigational drugs or treatments that consistently deliver on time to patients while ensuring that supply chain performance supports published study milestones. You will review and influence clinical protocols relative to investigational product supply and determine optimal, patient-focused, risk-adjusted and cost-effective supply plans. You will act as the primary interface between supply chain and the clinical study team, ensuring accurate and timely communication across all partner organisations. This role supports Phase I–IV GSK-sponsored clinical studies, investigator-sponsored trials and compassionate use studies.

Leads the MES platform for clinical manufacturing, ensuring the roadmap and delivery model support business needs. Collaborates across manufacturing, quality, and technology teams to deliver compliant, scalable, and sustainable digital capabilities. Owns the MES product roadmap and backlog, prioritizing features aligned to business value and delivery capacity. Ensures product compliance, validation, and operational sustainability. Leads product releases, monitors performance, and manages improvement actions.

Leads CMC regulatory strategy for development and lifecycle activities. Prepares and authors technical regulatory documents to support submissions. Identifies and mitigates risks associated with submission data. Mentors staff and manages projects.

Leads a global labelling team for oncology products, ensuring clear, compliant labels that support patient care and product success. Manages the GSK labelling process from early development through lifecycle management. Provides strategic direction for labelling governance and advises on labelling issues.

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Lead the Business Unit Specialty Care for BeLux, driving commercial strategy, launches, and portfolio growth. Collaborate with cross-functional teams and external stakeholders to improve patient access and shape healthcare policy. Translate global strategy into local plans, manage financial performance, and build a high-performing team.

Commissioning & Qualification (C&Q) Engineer with 4-6 years of experience needed to support equipment and system qualification activities (FAT, SAT, IOQ) in a regulated pharmaceutical environment. Will ensure tests are properly defined, executed, and documented, in line with internal procedures, GxP expectations, and leveraging strategies.

Provides day-to-day QA oversight for R&D operations related to clinical manufacturing and testing activities. Reviews and approves deviations, change controls, CAPA, and technical records. Leads or supports investigations and root cause analysis for quality events. Monitors quality metrics, performs trend analysis, and drives continuous improvements. Coaches and advises cross-functional teams on quality expectations, data integrity, and documentation best practices.

Senior Software Engineer needed with 5+ years of experience in programming and SQL. Proven ability to deliver high-quality software through clean code, testing, and code reviews. Must have strong technical skills, a creative mindset, and excellent algorithmic and conceptual thinking.

Technical Presales Consultant needed. Bachelor's or Master's degree in a relevant field with excellent communication skills and fluency in English. Strong technical aptitude, analytical mindset, and problem-solving skills required.

Global Production and Materials Demand Planner needed to support the company's ambitious goals of positively impacting the health of 2.5 billion people by the end of the decade.

This 6-month internship supports operational Supply Management activities in the planning department. Assisting the Senior Planning Manager, the intern will work on market launch activities, shipment distributions, data management, and project support.

Leads CMC activities for vaccine development projects in the United States. Coordinates technical input across quality, manufacturing, analytical development, and regulatory to enable timely deliverables. Prepares, reviews, and approves CMC documentation for regulatory filings and meetings with health authorities. Represents the CMC voice in cross-functional project meetings and drives decisions to resolve technical or programmatic issues. Mentors and coaches team members and supports capability building.

Lead the Business Unit Specialty Care for BeLux, driving commercial strategy, launches, and portfolio growth. Collaborate with cross-functional teams and external stakeholders to achieve growth and profitability targets.

Data Analyst / SQL Specialist will create reports, write and review SQL queries, and analyze existing queries for accuracy and efficiency. Must have strong SQL experience, attention to detail, and the ability to translate business needs into reliable data outputs.

Leads end-to-end clinical supply planning and delivery for assigned investigational assets. Works with clinical teams, quality, regulatory, and external partners to design patient-focused, risk-adjusted supply strategies. Manages clinical packaging, labeling, and distribution activities. Oversees Interactive Response Technology (IRT) specifications, testing, and maintenance. Tracks program costs, manages budgets, and reports status to stakeholders.

Develop and implement manufacturing and assembly methods for furniture and structures, respecting deadlines, budgets, and aesthetic constraints. Model complex objects, propose technical solutions, select hardware, and program CNC machines. Transfer manufacturing documents to the workshop and secure the supply of goods.

The Senior Programme Manager leads the planning and delivery of complex programmes that support GSK's strategic objectives. The role manages projects from initiation to completion, tracks benefit delivery, and oversees end-to-end project/programme management. Responsibilities include defining project scope, mobilizing project teams, managing budgets, and ensuring project compliance with GSK's program and portfolio management structures. The Senior Programme Manager also facilitates stakeholder engagement, provides project updates, and manages risks and escalations.

Internal Audit Manager will conduct comprehensive audits to assess risk management, business processes, financial reporting, and compliance. Responsibilities include performing the full audit cycle, identifying control deficiencies, and recommending solutions. Requires 8+ years of experience as an Internal Auditor, proficiency in data analytics, and fluency in English.

The Study Optimization Manager develops and implements clinical supply strategies for high-value clinical trials using advanced modeling techniques. Responsibilities include building and managing demand and supply models, analyzing complex data, and collaborating with stakeholders to optimize supply chain decisions.