52 English-speaking jobs in Wavre

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.

Leads the Site MSAT team in Belgium, ensuring successful execution of clinical trials.

Project Manager to lead and oversee complex digital projects within a road management program. Manage project scope, budgets, timelines, and risks while ensuring alignment with business objectives. Coordinate cross-functional teams and stakeholders. Proven experience in road management and agile software development practices required.

The Clinical Labelling Compliance Lead will oversee clinical labelling content compliance for clinical supplies across R&D. This role involves shaping processes, facilitating decision-making, and supporting audits and inspections. The successful candidate will work with a third-party to identify and maintain industry and country-specific requirements and translate these into compliant "Regulatory Rules".

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 with cross-functional teams. Prepare and review device documentation (DHF, RMF, usability engineering documentation).

Strengthen Environmental Monitoring (EM) and QA oversight across three GMP production buildings. Design monitoring tools, lead inspections, and author/review EM documentation to ensure compliance and continuous improvement.

Provides high-level administrative and organizational support to the Regional President. Manages complex calendars, schedules meetings, and coordinates travel arrangements. Prepares correspondence, presentations, and reports. Organizes regional leadership meetings and events.

Leads the sales team, develops and manages the sales and marketing budget, and implements the brand's sales strategy. Oversees sales channels, builds relationships with key accounts, and participates in revenue management strategies. Responsible for pre-opening sales activation, business development, and managing sales activities. Collaborates with marketing, operations, and revenue management teams.

Leads the development and execution of regulatory strategies for assigned assets, ensuring compliance with GSK processes and regulatory requirements. Manages and develops a team of regulatory professionals. Collaborates with cross-functional teams to secure optimal labeling and support product development. Requires extensive experience in all phases of drug development and a deep understanding of regulatory requirements in key markets.

Guide teams in adopting Agile behaviors and ensure Scrum is fully understood and applied. Collaborate with a cross-functional group to enhance transparency, alignment, and delivery excellence within product development.

Visual Communication Specialist to design and produce marketing materials for a consultancy. Experience in graphic design, Adobe Creative Suite, and visual storytelling required.

Leads a multi-disciplinary Global Clinical Supply Planning team, ensuring medicine and vaccine delivery to patients. Owns end-to-end supply plans, balancing service, cost, and working capital. Partners with cross-functional teams to support launches, pack changes, discontinuations, and lifecycle events.

This internship focuses on end-to-end logistics and supply chain transformation. The intern will contribute to designing a new operating model, evaluating potential solutions, and improving existing supply chain processes. The role requires a Master's student in Supply Chain or a related field, fluency in English, and the ability to work both remotely and on-site.

Vulcain Engineering Belgium seeks a PEG process support Cryo unit to work on biotech and pharmaceutical projects. Responsibilities include PEG Cryogenic unit management, setting up technical files and maintenance procedures, and coaching production teams. The ideal candidate has a background in chemical process engineering and experience in the chemical industry.

The Executive Medical Director, Safety Evaluation and Risk Management (SERM) Scientific Excellence leads the definition and implementation of safety approaches for early-phase trials and studies involving vulnerable populations. This role serves as the study-independent chair of the internal Safety Review Committee, ensuring the scientifically sound review and interpretation of unblinded safety data. The position provides leadership in developing scientific capabilities within SERM teams and fosters a high-performing culture within Global Safety.

Senior SAP FI/CO Consultant supports customers in their financial transformation journeys, designing and implementing SAP S/4HANA solutions. Analyzes financial and controlling processes, translates business requirements into SAP solutions, and advises on best practices. Requires 3+ years of experience as a SAP FI/CO Consultant in S/4HANA environments.

Senior SAP Supply Chain Consultant to support customers in Belgium with SAP ECC and S/4HANA environments. Provide 2nd and 3rd level functional support, analyze and resolve issues, and implement functional changes. Requires 3+ years of experience as a Supply Chain Consultant with expertise in PM, MM, SD, or PP modules. Fluent in English, French or Dutch is a plus.

SAP BTP Developer designs, develops, and supports innovative solutions on SAP Business Technology Platform. Responsibilities include providing technical support, developing cloud extensions, integrations, and custom applications, and collaborating with functional consultants and customers.

Develop and implement manufacturing and assembly methods for furniture and structures, respecting deadlines, budgets, and aesthetic constraints. Model objects, propose technical solutions, select hardware, and program CNC machines.

Validation professional with 4+ years of experience in pharmaceutical environments. Develops, reviews, and approves validation documentation, including validation plans, protocols, and reports. Executes and coordinates validation activities, manages deviations, and ensures compliance with GMP standards.