49 English-speaking jobs in Sittard

Inspect, test, and paint gas cylinders used in industrial settings. Work in a small team of 2-3 colleagues, following strict guidelines to ensure quality and safety.

Internship focused on recycling vanadium-based waste into V2O5 for thermochromic window coatings. Tasks include optimizing synthesis, characterizing products, and data analysis. Requires chemistry background, lab experience, and good communication skills.

This role involves ensuring the safe and compliant storage, handling, and internal transport of Dangerous Goods. Responsibilities include interpreting Safety Data Sheets, identifying risks, advising stakeholders, and contributing to process improvements.

Leads and governs indirect tax compliance globally, defining policies, processes, and directives. Manages global indirect tax technology projects and relationships with advisors and tax authorities.

The IT Infrastructure Site Lead ensures the availability, security, and performance of IT services and infrastructure at a specific site. This role involves managing networks, servers, storage, and backups, leading a small IT team, and collaborating with global IT teams. The IT Site Lead also implements ITIL processes, drives service improvements, and maintains compliance with security policies.

Senior QA Officer to review and approve batch records, manage deviations, and ensure GMP compliance in a pharmaceutical manufacturing environment.

Inspect and certify gas cylinders and pressure equipment, ensuring compliance with safety and quality standards. Responsibilities include visual inspections, pressure testing, documentation, and maintenance.

Leads a team of 15 Biotech Associates in a GMP-regulated cell and gene therapy manufacturing environment. Ensures safe, compliant, and efficient operations across a 24/7 schedule. Partners with Production, QA, QC, and Manufacturing Compliance teams. Requires experience leading a manufacturing team in a regulated environment and a Bachelor's degree in a related scientific discipline or equivalent experience.

Production Team Lead to supervise and support a team of Biotech Associates in a GMP-regulated cell and gene therapy manufacturing environment. Oversee daily operations, ensure compliance, and drive continuous improvement.

Warehouse Employee Parcels needed at Samsung SDS in Born. Duties include receiving and checking goods, picking and packing orders, and maintaining a clean and safe workplace. Experience with pick & pack is required.

Prepares printers for customer use, processes returns, handles damage to products and packaging, communicates with customers, and assists other departments.

Supports daily manufacturing operations by ensuring materials, equipment, and work areas are prepared and readily available. Follows procedures and GMP regulations to maintain high quality and safety standards in a cleanroom environment.

Workforce Europe seeks experienced Timmermen / Carpenters for residential, commercial, and industrial projects in the Netherlands. Install wooden structures, read technical drawings, and ensure work meets safety and quality standards. Minimum 2 years experience required.

AI Engineer will design, develop, and optimize AI applications, translating business challenges into scalable solutions. Responsibilities include designing AI agents, chatbots, and data pipelines, collaborating with stakeholders, and ensuring AI model quality and performance.

Design, build, and improve AI-driven solutions for business processes and decision-making. Translate business requirements into robust solution designs and provide technical guidance on AI architecture and technology. Develop and maintain data pipelines, knowledge retrieval mechanisms, and contextual data solutions. Evaluate, test, monitor, and optimize AI models and applications. Collaborate with business stakeholders to identify AI use cases and deliver solutions in Agile DevOps teams.

Senior QC Associate plans, executes, and supports quality control activities for manufacturing areas, materials, utilities, and products. Performs laboratory assays, supports investigations, and writes QC documentation. Requires a degree in a laboratory-related field and 3-6 years of experience in a QC, GMP, or laboratory environment.

Operate production machines, perform quality checks, and maintain a safe work environment. Work in a rotating schedule across various workstations. Must have good English skills and a focus on accuracy.

Investigate deviations, lead root cause analysis, and implement CAPA within a cGMP biotech environment. Collaborate cross-functionally to ensure compliance, optimize processes, and drive continuous improvement.

Senior QA Officer to review and approve batch records, lead deviation investigations, and ensure GMP compliance in a pharmaceutical manufacturing environment.

Senior QC Associate responsible for planning, executing, and supporting quality control activities in a GMP-regulated environment. Duties include performing laboratory assays, supporting investigations, writing documentation, and providing guidance to junior colleagues. Requires a degree in a laboratory-related field and 3-6 years of experience in a QC, GMP, or laboratory setting.