18 English-speaking jobs in Turnhout

Design and build production-grade Power BI reports and dashboards. Responsibilities include gathering business requirements, developing DAX measures, using SQL, and presenting insights to stakeholders. Strong Power BI expertise is required.

Experienced Test Reporting Engineer needed for a financial services organization. Requires 5+ years experience, deep knowledge of Factoring processes, and expertise in IT testing and financial report validation.

E&I Lead to manage the E&I package from Basic Engineering through commissioning for a heavy-industry brownfield project. Requires 10+ years' experience in MV/LV systems, instrumentation, and managing interfaces.

E&I Lead to manage the E&I package from Basic Engineering through commissioning for a heavy-industry brownfield project. Requires 10+ years' experience in MV/LV systems, instrumentation, and managing interfaces.

Senior Business/Data Analyst needed for a long-term freelance role in healthcare/pharma. Design and evolve the data model for an analytics platform supporting a laboratory network, enabling scenario modeling and Digital Twin development.

Experienced Test Reporting Engineer needed for a financial services organization. Requires 5+ years experience, deep knowledge of Factoring processes, and expertise in IT testing and financial report validation.

Test Reporting Engineer needed to ensure accuracy of complex internal and financial reports in a Factoring IT ecosystem. Requires deep factoring domain expertise and IT testing proficiency. Must have 5+ years experience.

Experienced Database Engineer needed to develop, maintain, and optimize database solutions using Oracle PL/SQL and Jasper Reports. Requires 5+ years in database engineering and 3+ years with Jasper Reports.

SciPharm seeks a Quality Control Specialist to own component/raw material inspection and procurement. Responsibilities include supporting QMS, CAPAs, and audits. Requires 2+ years in Quality Control with EU supplier experience.

SciPharm seeks a Process Engineer to own improvements to in-house manufacturing processes. Responsibilities include implementing DMAIC projects and supervising local operators. Requires 5+ years in Life Sciences, Automotive, or Aerospace with Six Sigma and ISO13485 experience.

Mechanical Engineer for particle accelerator applications. Follow design, procurement, and commissioning of RF components for a high-power proton accelerator. Requires Master's in Industrial Engineering and 4+ years of engineering experience.

Mechanical Engineer for particle accelerator applications. Follow design, procurement, and commissioning of RF components for a high-power proton accelerator. Requires Master's in Industrial Engineering and 4+ years of engineering experience.

SciPharm seeks a Quality Control Specialist to own component/raw material inspection and procurement. Responsibilities include supporting QMS, CAPAs, and audits. Requires 2+ years in Quality Control with EU supplier experience.

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.

Design & Development Engineer will review, assess, and process technical documents for regulatory compliance. The role involves identifying gaps in documentation, coordinating document formatting, and maintaining design history files. Experience in medical device documentation, quality, or regulatory roles is required.

Leads design and development activities for implantable infusion products, ensuring compliance with FDA, EU MDR, and ISO standards. Manages a team of engineers and external partners, overseeing design controls, documentation, and clinical investigations. Collaborates with manufacturing, regulatory, and clinical teams.

Design & Development Engineer will review, assess, and process technical documents for regulatory compliance. The role involves identifying gaps in documentation, coordinating document formatting, and maintaining design history files. Experience in medical device documentation, quality, or regulatory roles is required.

Leads design and development activities for implantable infusion products, ensuring compliance with FDA, EU MDR, and ISO standards. Manages a team of engineers and external partners, overseeing design controls, documentation, and clinical investigations. Collaborates with manufacturing, regulatory, and clinical teams.