26 English-speaking jobs in Geel

Lead Software Engineer for R&D Technology designs and delivers solutions for next-gen R&D capabilities. This role bridges scientific needs with scalable technology, owning architecture, CI/CD, and integration across lab systems.

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.

Construction Manager role requires 10+ years in mechanical projects within pharmaceutical or oil and gas industries. Responsibilities include onsite coordination, schedule monitoring, and subcontractor supervision.

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.

Senior or Principal Scientist to manage and coordinate metabolite profiling and identification studies for drug discovery and development programs. Responsibilities include designing, planning, and conducting in vitro incubations, performing LC/MS analysis, and serving as a subject matter expert for biotransformations. PhD in a relevant field and hands-on experience in structure elucidation using mass spectrometry are required.

Warehouse Operator for LEGO department. Picks, packs, and prepares orders. Performs quality checks and moves goods. Requires manual dexterity, attention to detail, and ability to work in a 2-shift system. Training provided.

Develops and executes global category strategies for Clinical Manufacturing and CMC Product Development services, driving value through supplier relationships and risk management.

The EMEA Regional Security Director develops and implements security strategies, manages a team, and responds to security incidents across Europe, Middle East, and Africa.

Leads late-phase clinical development (P2b/3) of neuropsychiatry compounds. Develops and executes clinical development plans, designs trials, and prepares regulatory filings. Manages a matrix-based clinical team and oversees safety and medical activities. Requires an MD with post-doctoral training and 7+ years of clinical research experience, including 3+ years in phase II/III development.

MSAT Synthetics Drug Product External Site Principal Scientist provides technical oversight to external manufacturing sites. Handles technology transfer, product life cycle activities, and material qualification. Acts as technical coordinator for CMO process technology proficiency and implementation of MSAT Technology Roadmaps. Supports site lifecycle processes and technical assessment of change controls. Requires a bachelor's degree and 8+ years of relevant experience.

Lead Computer System Validation (CSV) & Data Integrity (DI) efforts, ensuring alignment with industry best practices and regulatory requirements. Oversee projects, manage resources, and drive change management initiatives. Deep understanding of CSV, DI, risk management, and pharmaceutical manufacturing environments is required.

Senior Data Scientist to apply advanced statistical modeling and data science techniques to optimize manufacturing performance in the biopharmaceutical industry.

Leads equipment qualification activities throughout the project lifecycle, ensuring compliance with GMP and company standards. Develops and reviews qualification documentation, coordinates activities with various departments, and provides technical guidance during installation and commissioning.

Experienced Quantity Surveyor/Contracts Manager needed to lead commercial and contractual activities for a pharmaceutical manufacturing facility construction project. Responsibilities include cost control, contract administration, and risk mitigation.

Design, develop, and improve industrial machinery and mechanical systems. Produce 2D drawings, 3D CAD models, and technical documentation. Collaborate with multidisciplinary teams to ensure seamless integration of designs.

LOTO Coordinator for electrical systems on construction projects in Belgium. Develops and manages LOTO plans, coordinates isolation, verifies zero-energy states, and ensures compliance with safety regulations and site SOPs.

EHS Advisor needed for pharmaceutical construction project in Geel. Develop and implement EHS programs, conduct safety inspections, ensure regulatory compliance, and investigate incidents. Requires a bachelor's degree in a related field, 5+ years of construction EHS experience, and 2+ years in pharmaceutical or regulated industry construction.

PM Group seeks an experienced Turnover Coordinator for a pharma construction project in Geel, Belgium. The role involves coordinating the systematic turnover of completed construction systems to commissioning, qualification, and operations teams. Responsibilities include developing turnover packages, managing schedules, facilitating inspections, and ensuring compliance with GMP requirements.

PhD Researcher to develop radiation-tolerant pixels for CMOS image sensors exceeding 1 MGray TID with low read noise. Work involves TCAD simulation, design, prototyping, and characterization.

Experienced EHS Advisor needed for pharmaceutical construction. Responsibilities include developing EHS programs, conducting safety inspections, ensuring regulatory compliance, and managing environmental aspects. Requires a Bachelor's degree and 5+ years of construction EHS experience.