35 English-speaking jobs in Geel

Provides strategic direction for Johnson & Johnson Innovative Medicine Combination Product & Device Development initiatives. Ensures design control procedures are harmonized and executed across multiple departments and sites. Drives the rapid, compliant, high-quality development, transfer, and lifecycle management of new drug-device combination products.

Supports Quality Assurance by applying best practices, documenting issues, and collecting feedback for continuous improvement. Assists with ensuring alignment with quality priorities and escalating quality, compliance, and system issues. Analyzes research and data related to regulatory changes and trends.

Data Scientist to support tech transfer, process optimization, and launch of biopharmaceutical products. Provides statistical and data science support across MSAT functions. Designs experiments, analyzes data, and prepares reports. Requires a BS, MS, or PhD in Data Sciences, Statistics, or related field with relevant industry experience.

Leads governance on capability improvements for a global business transformation initiative standardizing core business processes across Plan, Source, Make, Quality, Deliver, and Data. Partners with functional template owners, Technology, and Master Data to sustain and manage system content, configuration, and data excellence. Ensures compliance with IM and Transcend processes and collaborates with IT to develop integration points. Develops and maintains support infrastructure, including documentation and Change Control Boards, and leads continuous improvement initiatives.

Senior Pilot Plant Engineer to lead scale-up activities from lab to pilot scale, including process transfer, troubleshooting, and optimization. Develop and deploy process models to support design, scale-up, and performance. Collaborate cross-functionally and provide training to staff. Requires a minimum of 5 years of experience in chemical development operations, process development, or scale-up. Master's or Ph.D. in chemistry, chemical engineering, bio-engineering, or related field. Experience with PAT tools and process simulation software. Strong safety, quality, and compliance orientation. Excellent project management, communication, and problem-solving skills.

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 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.

Associate Director will accelerate complex clinical development programs through integrated planning, risk management, and cross-functional collaboration. Responsibilities include creating study schedules, identifying acceleration opportunities, and managing budgets, timelines, and resources. Requires a Bachelor's degree, 8+ years of experience in clinical development, and expertise in project management methodologies and tools.

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.

Leads the Transcend program, a global business transformation initiative modernizing transactional processes and aligning them to a single ERP platform. Designs and owns strategic change plans, leads a team of change practitioners, and collaborates with business teams to ensure workforce readiness.

Senior Data Scientist to apply advanced analytics to optimize biopharmaceutical manufacturing processes. Collaborate with cross-functional teams to solve complex challenges, design experiments, and translate data into actionable insights. Requires expertise in statistics, data science, and experience in the pharmaceutical 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.

As a Qualification Engineer (Equipment), you will support engineering teams in introducing and optimizing installations and processes at a leading company in Geel. You will review and approve qualification and validation documents, advise on cGMP compliance, and contribute to the implementation of improvement processes.

Qualification Engineer needed to support engineering teams in qualifying equipment. Review and approve qualification and validation documents. Provide advice on cGMP aspects and compliance. Experience with qualification or validation activities in the pharmaceutical sector required.

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.

Lead the scientific strategy for dissolution and in vitro release (IVR) science, supporting global portfolio development. Design and implement robust dissolution methods, scale-up studies, and automation/AI workflows. Translate science into regulatory submissions and engage with Health Authorities. Mentor scientists, support matrix teams, and deliver scientific narratives to senior management.

Experienced Mechanical QA/QC Line Walker needed for a 12-16 month contract in Belgium. Responsibilities include mechanical line walks, piping inspections, and ensuring defect-free installations. Requires previous pharmaceutical QA/QC or Mechanical Line Walking experience and knowledge of piping systems, isometric drawings, and welding.

MSL Engineering seeks an MEP Coordinator to manage HVAC and electrical scope of work for life science capital projects. The role involves overseeing on-site installations, coordinating with subcontractors and vendors, and ensuring compliance with URS, specifications, and client standards. Requires 4+ years' experience in M&E coordination, proficiency in Navisworks, and strong communication and organizational skills.

Design, develop, and deploy machine learning models for real-world applications at Virto Solar. Collaborate with engineers, product managers, and domain experts to integrate AI solutions into production software. Contribute to the architecture of the AI platform and explore new AI technologies.

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.