Company Our client is a large, fast-paced manufacturing environment with a high-volume logistics operation. The organization focuses on operational performance, safety, quality, and continuous improvement, working closely across logistics, production, maintenance, planning, and quality teams. Job Description We are looking for a Logistics Continuous Improvement Specialist to drive structured, data-led improvements across the logistics organization. This person will identify operational bottlenecks, translate them into clear improvement initiatives, and lead implementation on the shop floor—ensuring solutions are sustainable and repeatable. Responsibilities – Translate operational issues into data-driven improvement actions and ensure fast implementation on the shop floor – Use structured improvement routines and ways of working (e.g., daily direction setting, problem solving, work process improvement) to drive results – Ensure improvements are systematic and repeatable, not one-off fixes – Coach and support logistics teams in continuous improvement and problem-solving techniques – Analyze and optimize logistics flows including inbound, storage, picking, and line feeding – Reduce handling, waiting times, and inefficiencies across warehouse processes – Lead the logistics side of Management of Change for improvement initiatives, including projects with investment scopes up…

Technical Operator (Automated Lines) RED The Company Our client is a leading global biotechnology company dedicated to developing, manufacturing, and delivering innovative medicines. Operating within a GMP-regulated manufacturing environment, the organization is committed to quality, compliance, operational excellence, and continuous improvement. Role Description We are looking for an experienced Technical Operator (Automated Lines) to support highly automated manufacturing operations. In this role, you will operate, troubleshoot, and optimize automated production equipment while ensuring compliance with GMP standards. You will play a key role in maintaining production efficiency, minimizing downtime, supporting continuous improvement initiatives, and delivering high-quality products in a shift-based manufacturing environment. Key Responsibilities Operate, monitor, and optimize automated production equipment in accordance with SOPs and GMP requirements. Troubleshoot equipment issues, perform root cause analysis, and optimize machine performance. Complete accurate production documentation using SAP/MES while ensuring GMP compliance. Participate in triage meetings and collaborate with Production, QA, and Maintenance & Engineering teams to resolve technical issues. Support continuous improvement initiatives through Lean Manufacturing and structured problem-solving methodologies. Perform equipment set-up, changeovers, cleaning activities, and ensure safe shift handovers. Key…

Support Operator (Green) The Company Our client is a leading global biotechnology company committed to discovering, developing, manufacturing, and delivering innovative medicines. Operating in a GMP-regulated manufacturing environment, the company is focused on quality, safety, and operational excellence to improve patients’ lives worldwide. Role Description We are looking for a motivated Support Operator to support daily manufacturing operations across multiple production lines. You will help ensure efficient production by preparing materials, supporting line activities, and maintaining compliance with GMP, safety, and quality standards. This role requires flexibility, teamwork, and a willingness to work in a shift-based manufacturing environment. Key Responsibilities Support production activities in line with SOPs and GMP requirements. Prepare materials and assist with production line set-ups and changeovers. Ensure compliance with GMP, safety, and quality standards. Maintain a clean, safe, and organized production environment. Work closely with operators and production teams to ensure smooth production flow. Key Requirements MBO Level 2 qualification (or equivalent). Experience in a production or manufacturing environment is preferred. Fluent in English. Willingness to work in a shift-based manufacturing environment. Comfortable working under GMP…

Company – General Description: A well-established organization committed to safety, operational excellence, and continuous improvement within the manufacturing and chemical industries. They value technical expertise, leadership, and a proactive approach to plant maintenance and reliability. Job Description – Summary of the Role: We are seeking a dedicated Maintenance and Reliability Operations Lead to oversee plant maintenance, drive continuous improvement initiatives, and lead a team of technical specialists. The ideal candidate will ensure safe and efficient operations while fostering a culture of operational discipline and excellence. Responsibilities – More Detailed: •    Ensure a safe work environment and compliance with all safety policies. •    Manage the plant’s mechanical, electrical, and instrumentation maintenance functions, reporting directly to the Plant Manager. •    Lead and develop front-line supervisors within the Maintenance & Reliability teams. •    Organize, plan, and control maintenance activities and oversee long-term maintenance strategies through business planning. •    Specify maintenance tasks by deploying Bill of Materials and proactively analyze data for predictive and preventive maintenance. •    Meet operational, budgetary, and timeline expectations. •    Classify maintenance levels and track expenditure in relation to the…

Over het Bedrijf Deze internationale voedselproducent staat voor kwaliteit, voedselveiligheid en continue verbetering. Binnen de organisatie wordt gewerkt volgens de hoogste kwaliteits- en certificeringsnormen, waarbij samenwerking, innovatie en procesoptimalisatie centraal staan. Rolomschrijving Als Quality Engineer ben je verantwoordelijk voor het beheren en verder ontwikkelen van het kwaliteitsmanagementsysteem (QMS) en het waarborgen van de naleving van wet- en regelgeving op het gebied van voedselveiligheid en kwaliteit. Je leidt audits, analyseert kwaliteitsafwijkingen en initieert verbeterprojecten om processen structureel te optimaliseren. Je bent de inhoudelijke sparringpartner voor Productie en Management op het gebied van kwaliteit en compliance. Belangrijkste Verantwoordelijkheden Beheren en verbeteren van het Quality Management System (QMS) en kwaliteitsprocessen Leiden van interne en externe audits en opvolgen van verbeteracties Bewaken van certificeringen zoals IFS, HACCP, RSPO en Beter Leven Uitvoeren van root cause analyses bij kwaliteitsafwijkingen en implementeren van structurele verbetermaatregelen Initiëren en begeleiden van kwaliteits- en procesverbeteringsprojecten Opstellen en analyseren van KPI’s, kwaliteitsrapportages en trendanalyses Adviseren van Productie en Management over kwaliteits- en voedselveiligheidsvraagstukken Onderhouden van contacten met laboratoria, certificerende instanties, leveranciers en andere externe partijen Vereisten Minimaal een HBO-opleiding in…

Company Our client is a leading manufacturing organization dedicated to producing high-quality medicines within a regulated GMP environment. They focus on operational excellence, continuous improvement, and delivering safe, top-quality products to patients worldwide. Their team values technical expertise, collaboration, and a proactive approach to process development. Role Description We are looking for an Operator Clinical Labelling & Packaging to support the manual labelling, packaging, and assembly of clinical products for global clinical trials. Working in a GMP-regulated environment, you will ensure products are packaged accurately and in compliance with Standard Operating Procedures (SOPs), helping deliver high-quality medicines to patients worldwide. Responsibilities – Perform manual labelling, packaging, and assembly of clinical products. – Follow GMP guidelines and SOPs to ensure quality and compliance. – Execute batch-related logistics and complete required documentation. – Conduct quality checks and escalate any deviations or issues. – Support continuous improvement initiatives and maintain training compliance. – Work collaboratively in both room temperature and occasional cold-room (2–8°C) environments. Requirements – Experience in packaging, manufacturing, production, or assembly; GMP/pharma experience is a plus. – Strong attention to detail…