50 English-speaking jobs in Sittard

Project Lead Quality Control coordinates QC technology transfers and manages project plans for cell and gene therapies. Requires strong organizational skills, stakeholder management, and a technical background in biotech or pharmaceutical sciences.

QC Technical Expert in pharmaceutical microbiology. Resolve complex microbiological challenges, support testing, and guide quality standards. Requires a relevant degree and GMP experience.

Technical Production Worker inspects and refurbishes bundles of gas cylinders. Duties include dismantling, assembling, sanding, blasting, painting, and replacing valves. Requires manual skill, physical stamina, and attention to safety.

Assistant Supervisor co-manages daily warehouse operations, guiding 20-30 employees. Responsibilities include coordinating activities, monitoring KPIs, and driving process improvements in a dynamic logistics setting.

Senior Specialist to improve aseptic behavior and contamination control in sterile manufacturing. Responsibilities include hands-on training, coaching, and administering certification programs within a GMP environment.

QA Specialist/Officer II supports GMP operations by reviewing quality documentation, approving quality events, and providing QA oversight during manufacturing. Requires a relevant scientific degree and GMP experience.

Lead and develop a QA team supporting Cell & Gene Therapy manufacturing operations. Ensure cGMP compliance, manage deviations, CAPAs, and quality documentation. Requires 5+ years of QA experience in cGMP and 2+ years in leadership.

Lead strategic and tactical Fleet initiatives, managing scope, budgets, risks, and cross-functional teams. Define project objectives and ensure successful implementation of improvements across Boels.

Customer Support Supervisor to help implement support for a new client in an international logistics environment. This role involves team development, coaching, managing KPIs, and handling escalations.

Deliver hands-on training and coach employees to maintain high standards of aseptic practice in manufacturing environments. Monitor aseptic behaviors, analyze trends, and improve training standards. Requires a science background and GMP training experience.

Experienced leader needed for Production Team Lead role in a regulated manufacturing environment. Responsibilities include leading a team of 15, ensuring safe and efficient operations, and driving GMP compliance. Requires background in biotech or pharma.

Join CEVA Logistics as a Logistics Employee for Metso. This full-time role involves order picking heavy components, loading, and unloading shipments using EPT or forklift. Must be physically fit and willing to work 2 shifts.

Logistics Supervisor responsible for daily warehouse operations in Consumer Products or High-Tech divisions. Duties include coordinating processes, meeting KPIs, managing staff, and leading teams. Requires experience with ERP/WMS systems.

Finance Business Partner supporting Capital Investment. Lead performance management, cost excellence, inventory, and working capital. Provide financial lead for capital investments, including business case analysis and reporting.

Support daily manufacturing in a GMP cleanroom environment. Prepare, transport, and verify materials. Perform cleanroom support, cleaning, and area preparation. Requires MBO qualification or equivalent in a technical, logistics, production, or scientific field.

Handle supply chain activities including goods receipt, storage, and final product shipments within a GMP Warehouse and Logistics team. Requires technical education or equivalent experience and business-level English.

As Product Owner Fleet, you turn business priorities into digital solutions for the international Fleet supply chain. You translate the roadmap into clear objectives, refine user stories, and guide development teams.

Support warehouse operations in a high-tech logistics environment. Investigate issues, analyze data using SAP and Excel, and implement sustainable process improvements for a new customer operation.

Lead a Quality Control team supporting manufacturing through reliable testing and monitoring. Responsibilities include team development, coordinating QC testing, and reviewing results, ensuring product quality and patient safety. Requires QC experience in regulated environments.

Senior QA Compliance Specialist maintains and strengthens the Quality Management System at the Geleen site. This role ensures GMP compliance, supports inspection readiness, and drives continuous improvement.