51 English-speaking jobs in Sittard

Process Assessment and Validation Scientist II performs assessments for new process implementation, validation, and post-TT support. Responsibilities include GMP evaluation of process design, APS, and equipment, and leading root-cause investigations.

Handle European customer operations by processing orders and quotations in SAP. Act as a primary contact, managing inquiries, returns, and issues while collaborating with internal teams. Strong English and attention to detail are required.

QA Officers (Junior, Medior, Senior) support GMP operations by reviewing batch records, approving documentation, and providing quality oversight in life sciences manufacturing. A relevant scientific degree and understanding of GMP principles are required.

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 performs inspection and maintenance on gas cylinder bundles. Duties include dismantling, assembling, sanding, blasting, painting, and valve replacement. Requires manual skill, physical stamina, and attention to detail.

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.

Associate Commercial Lab Engineer supports testing in the European demonstration center. This role assists with equipment setup, test execution, documentation, and customer demonstrations. A technical background is preferred.

Senior Specialist to maintain aseptic behavior and contamination control in sterile manufacturing. Responsibilities include training, coaching, and improving aseptic practices, GMP modules, and supporting contamination investigations.

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 and develop a QA team supporting Cell & Gene Therapy manufacturing operations. Ensure cGMP compliance, manage deviations, CAPA, and support product release. Requires 5+ years of QA experience in cGMP environments.

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 team leader needed for production in biotech or pharma. Lead a team of 15 in a 24/7 environment, ensuring safe, efficient manufacturing and GMP compliance. Bachelor's degree or equivalent experience required.

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.

Support daily manufacturing in a GMP cleanroom environment. Prepare and verify materials, perform cleanroom support, and conduct routine checks to ensure production readiness. Requires MBO qualification or equivalent technical education.

Support daily manufacturing in a GMP cleanroom environment. Prepare, transport, and verify materials while performing cleanroom support activities. 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.