163 English-speaking jobs in Liège

Quality Assurance professional with 5+ years experience in the pharmaceutical industry. Expertise in GMP, GDP, data integrity, and CSV. Strong knowledge of deviation, CAPA, and change control management. Experience supporting audits and regulatory inspections.

Quality Assurance professional with 5+ years experience in the pharmaceutical industry. Expertise in GMP, GDP, data integrity, and CSV. Strong knowledge of deviation, CAPA, and change control management. Experience supporting audits and regulatory inspections.

QA professional with 5+ years of experience in the pharmaceutical industry required. Strong knowledge of EU GMP, GDP, and data integrity. Experience with deviation, CAPA, and change control management, CSV, and eQMS systems.

Quality Assurance professional with 5+ years experience in the pharmaceutical industry. Expertise in GMP, GDP, data integrity, and CSV. Strong knowledge of deviation, CAPA, and change control management. Experience supporting audits and regulatory inspections.

Frontend Engineer to build and evolve customer-facing web applications using React and TypeScript. Collaborate with cross-functional teams to deliver new features and contribute to engineering best practices.

Quality Assurance Specialist applying and maintaining the Pharmaceutical Quality System (PQS) per GMP/GDP and regulations. Reviews and approves GMP documentation, manages deviations, CAPAs, and change controls. Supports qualification/validation, risk assessments, and supplier quality.

Talent Acquisition Specialist sourcing, screening, and qualifying IT and engineering candidates for clients. Manage recruitment pipelines, present shortlisted profiles, and contribute to candidate community building.

QA/RA Officer to develop, maintain, and improve the Quality Management System (QMS). Manages QMS processes, reviews manufacturing documentation, and leads/participates in QA/RA projects.

QA/RA Officer to develop, maintain, and improve the Quality Management System (QMS). Manages QMS processes, reviews manufacturing documentation, and leads/participates in QA/RA projects.

QA/RA Officer to support the development, maintenance, and improvement of the Quality Management System (QMS) ensuring compliance with ISO13485, IVDR, MDSAP, FDA, and other regulatory requirements. Responsibilities include managing QMS processes, reviewing documentation, participating in audits, and ensuring product registration.

Project Manager for multi-country research projects, combining research delivery, data management, and client advisory. Requires 5+ years of experience in survey research, advanced SPSS skills, and strong project management abilities.

Postdoctoral researcher to develop nano-antibody therapeutics targeting proteases involved in chronic inflammatory diseases. Responsibilities include protein production, nano-antibody design and characterization, in vitro and in vivo testing, and publication of findings. Requires a PhD in a relevant field, experience with recombinant protein expression, and computational antibody design.

RF Engineer needed for a permanent position in the Wallonian region of Belgium. Design, analyze, integrate, and test RF and microwave systems for space communication technologies. Collaborate with multidisciplinary teams throughout the product lifecycle. Bachelor's degree in a related field and proven RF engineering experience required.

Financial Controller needed for market-leading automotive company in Puurs. Evaluates financial performance, mitigates risks, and optimizes business processes. Requires Bachelor's/Master's in Finance/Accounting/Economics, experience in finance, and advanced Excel skills.

We are seeking experienced CNC operators, setters, and programmers for advanced manufacturing roles in Belgium. Set up and operate CNC machines, read technical drawings, and ensure precise production of custom components. Relocation assistance is available.

Full-Stack Engineer to build and improve the Prezly platform, using React, TypeScript, PHP (Symfony), and PostgreSQL. Collaborate with product and design to ship features and improve existing product functionality.

QA Specialist to oversee quality activities for Contract Manufacturers (CMOs), ensuring GMP compliance. Reviews deviations, CAPAs, change controls, and product market complaints. Requires a scientific degree, 5+ years in a cGMP environment, and proficiency in English, SAP, and Veeva.

Firmware Engineer to develop embedded software for semiconductor portfolio. Requires experience with Linux, PCIe devices, DTM, and embedded development tools. Strong C/C++, scripting, and problem-solving skills are essential.

The LPO & GET Lead for Computer System Validation (CSV) & Data Integrity (DI) will own site-level CSV/DI processes, ensuring compliance with regulatory requirements. The role requires deep understanding of CSV/DI in a pharma manufacturing environment, including 21CFR Part 11, EU Annex 11, and GAMP guidelines.

Process Engineer to design, optimize, and improve sterile fill and finish processes in the biotech or pharmaceutical industries. Lead NPI and technical transfer for new customer projects. Develop and execute validation strategies and process risk assessments.