38 English-speaking jobs in Geel

Vulcain Engineering is looking for a Junior QA Engineer to support deviation management activities during production campaigns in a GMP environment. You will work closely with experienced QA and production teams, contributing to quality and compliance while developing your expertise in a fast-paced pharmaceutical setting.

The Transcend PMO Senior Operations Manager will lead PMO operations across program phases, ensuring effective governance, communication, and high-quality inputs for decision forums. The role will drive integrated planning, handle RAID and change control processes, supervise schedule management, and ensure consistent and transparent status reporting. The PMO Senior Operations Manager will also lead and develop a diverse PMO operations team, coach and mentor team members, and partner with Global Program Managers and PMO leadership.

Provides strategic and technical leadership for data generation initiatives, ensuring scientific rigor across Johnson & Johnson's portfolio. Leads the design of study designs and statistical analyses aligned with Payer/HTA expectations.

Lead multifunction team to modernize pharma ERP and end-to-end logistics globally. Integrate logistics and transportation into global ERP template and deliver design within program scope.

Associate Director will lead initiatives to improve portfolio planning system processes, ensuring alignment with organizational goals. The role will support the development of portfolio data quality metrics and lead data quality efforts to address gaps. The Associate Director will partner with business teams to implement process improvements and technology solutions.

Leads the implementation of biomarker strategies for neuroscience clinical development programs, collaborating with cross-functional teams to ensure alignment with program objectives and regulatory requirements.

Experienced Quality Lead needed for a major pharmaceutical construction project in Belgium. Responsibilities include implementing quality management systems, ensuring GMP compliance, and managing quality activities throughout construction and validation.

As a Principal within the HE/HTA/V&A Practice, you will deliver outstanding client service, build trusted relationships, and develop business opportunities. You will oversee projects, identify new opportunities, and present educational materials. You will also lead thought leadership initiatives and mentor others.

The CQV Engineer will qualify assigned biopharmaceutical processing systems and utilities, ensuring compliance with EU and US GMP regulations. Responsibilities include generating validation documents, verifying technical documentation, and executing IQ/OQ protocols.

The CQV Engineer will qualify assigned biopharmaceutical processing systems and utilities, generating validation documents and executing IQ/OQ protocols. The role requires knowledge of GMP regulations, pharmaceutical plant qualification, and process & clean utility design.

The CQV Engineer will qualify assigned biopharmaceutical processing systems and utilities, ensuring compliance with EU and US GMP regulations. Responsibilities include generating validation documents, verifying technical documentation, and executing IQ/OQ protocols.

The CQV Engineer will qualify assigned systems, including biopharmaceutical processing systems and utilities, according to EU and US GMP regulations. Responsibilities include generating validation documents, verifying technical documentation, and executing IQ/OQ protocols.

The CQV Engineer will qualify assigned biopharmaceutical processing systems and utilities, generating validation documents and reports according to EU and US GMP regulations.

Experienced Cost Controller needed for a long-term (24+ months) pharmaceutical CAPEX program in Geel, Belgium. Manage cost reporting, forecasting, and budget control for a brownfield expansion project.

The CQV Engineer will qualify assigned biopharmaceutical processing systems and utilities, ensuring compliance with EU and US GMP regulations. Responsibilities include generating validation documents, verifying technical documentation, executing IQ/OQ tests, and reporting on progress.

Senior Project Scheduler needed for a major €500M+ pharmaceutical brownfield expansion in Belgium. Develop integrated master schedules, manage critical path analysis, and coordinate shutdown planning. Requires 10+ years of experience with Primavera P6 and brownfield projects.

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.

MSAT Upstream Scientist will drive technology transfer, optimize manufacturing processes, and support continuous improvement initiatives. Requires PhD in Life Sciences with 3+ years experience or Master's degree with 5+ years experience in process development or MSAT.

MSAT Scientist with expertise in upstream cell culture processes needed for technology transfer, process optimization, and support of commercial manufacturing. Requires a Master's or PhD in Life Sciences and 3-5 years of relevant experience.

MSAT Scientist with expertise in upstream cell culture processes needed for technology transfer, process optimization, and support of commercial manufacturing. Requires a Master's or PhD in Life Sciences and 3-5 years of relevant experience.