24 English-speaking jobs in Geel

Principal Scientist, CMC Regulatory Affairs - Combination Products provides regulatory subject matter expertise for drug-device combination products. This role develops and executes regulatory strategies for submissions and lifecycle management globally.

Detail-driven QA Specialist needed to support operations at a multiproduct facility during digitalization. Responsibilities include drafting quality documentation, reviewing electronic Master Batch Records in MES PAS-X, and ensuring cGMP compliance.

Quality Officer needed for temporary contract to perform QA review of batch-related documentation in a GMP environment. Requires a scientific degree, GMP experience, and familiarity with QMS and MES systems.

QA Specialist needed for Drug Substance manufacturing. Responsibilities include quality reviews of batch records, approving operational documents, and providing quality oversight. Requires a Master's degree in a scientific field and knowledge of cGMP.

Manage scope, budget, and schedules for complex data center projects. Coordinate multidisciplinary teams and act as a key link between Belgian and international project groups. Requires a Master's in a technical field and 5+ years of project management experience.

Senior E&I Engineer needed for chemical and API process installations in Belgium. Requires strong experience in Electrical & Instrumentation, specifically ATEX and hazardous-area environments. Focus on process installations.

Senior DeltaV Engineer needed for chemical/API process installations in Belgium. Support engineering, configuration, and implementation of Emerson DeltaV systems across the project lifecycle. Strong hands-on experience required.

Senior technical and operational leader accountable for end-to-end delivery of high-complexity capital investments at an API manufacturing site. This role manages a business-critical program for capacity expansion, ensuring safety, quality, and budget adherence.

QA Specialist will provide quality support to operations activities in a multiproduct facility. Responsibilities include preparing and reviewing quality documentation, providing quality support and expertise, ensuring compliance with SOPs and regulations, and supporting cross-departmental collaboration.

Director MTO Operational Excellence shapes site strategy, managing continuous improvement processes and governance. This role leads OPEX initiatives, drives value stream mapping, and builds site capability.

Lead early design inputs and technical strategy for synthetic drug substance (API) manufacturing processes. Provide expertise in unit operations like chemical reaction, crystallization, and filtration, ensuring cGMP compliance and process safety.

MSAT Process Engineer needed to scale up and optimize biological manufacturing processes in cell culture or purification. Requires a Master's or PhD with 3-5 years of relevant experience in Life Sciences.

Pipefitter role for Data Centre construction. Responsibilities include installing carbon and stainless steel pipework, assembling chilled water systems, and interpreting isometric drawings. Requires experience in Data Centre or industrial projects and an EU Passport.

Construction Quality Engineer/Supervisor for a large-scale Pharmaceutical Construction Project. Responsibilities include verifying compliance, conducting inspections, managing quality documentation, and ensuring adherence to standards. Requires 3-7 years in construction quality.

Lead local gap and risk assessments in Life Sciences across IT, Lab, R&D, and Equipment. Develop Data Integrity master plans, ensuring compliance with FDA and EMA requirements. Requires strong project management and communication skills.

MSAT Process Engineer supports commercial manufacturing through process/method optimization and technology transfer. Focus is on cell culture or purification at lab/manufacturing scale, requiring strong scientific knowledge and GMP understanding.

Provide cleaning and ironing services to clients. Work independently, manage your schedule, and build a client base. Must be able to communicate in Dutch, English, or French.

Supervise mechanical installation teams for process equipment in pharmaceutical construction. Ensure compliance with GMP, FDA, and EMA standards while managing contractors, quality, and project schedules.

Mechanical Piping Superintendent role involving safety, construction, quality, and commercial oversight. Responsibilities include developing work packs, signing off test packs, and coordinating disciplines. Requires 3-5 years' experience and knowledge of piping isometrics and P&IDs.

Coordinate systematic turnover of construction systems in pharmaceutical facility projects. Develop turnover packages, manage schedules, and ensure documentation meets GMP and regulatory compliance standards.