Logistics CI Specialist, Cuijk, Noord-Brabant

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 Requirements Technical qualification (MBO, VAPRO B, or equivalent) with at least 3 years of experience in an automated manufacturing environment. Experience working in a GMP-regulated production environment, preferably within the pharmaceutical or food industry. Knowledge of SAP/MES systems and continuous improvement methodologies such as Lean, Six Sigma, 5 Why, RCA, Kaizen, TPM, or SMED. Strong technical understanding of automated equipment, including mechatronics, pneumatics, electronics, sensors, and control systems. Fluent in English with excellent analytical, problem-solving, and communication skills. Willingness to work in shifts and thrive in a structured, quality-focused manufacturing environment. Other Information Are you interested in this or another role? click the apply button below and I will contact you as soon as possible  

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 procedures and following strict instructions. Team player with a reliable, flexible, and proactive attitude. Other Information  Are you interested in this or another role? click the apply button below and I will contact you as soon as possible

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 business plan, making adjustments as needed. •    Develop and manage the maintenance budget and lead TAR (Technical Assistance Repair) projects. •    Oversee plant CMMS (SAP PM, MM) systems, ensuring proper KPI tracking, scheduling, and staff performance management. •    Conduct root cause failure analyses and support process hazard analyses (PHA). •    Ensure maintenance teams are trained and compliant with PSM standards. •    Drive optimization of work preparation processes for better resource utilization. •    Implement tools for root cause analysis of asset failures and ensure corrective actions are executed. •    Promote continuous improvement initiatives by identifying gaps and following through on improvement actions. •    Foster an innovative environment by collecting and promoting departmental improvement ideas. •    Lead efforts to develop and sustain a culture of operational discipline across the team. •    Engage and mentor maintenance and reliability staff, supporting their development and retention. •    Facilitate workshops and promote a culture of continuous improvement within the team. Requirements – Key Points Only: •    Bachelor’s degree in engineering or business with proven engineering knowledge. •    Extensive experience (10+ years) in maintenance or operations, with leadership experience. •    Strong expertise in reliability engineering and project management. •    Certification in Six Sigma / Lean, with advanced knowledge of manufacturing and business systems methodologies. •    Experience leading TAR projects and deploying continuous improvement tools. •    Proficiency in problem-solving using A3 thinking. •    Preferably experience in the chemical industry. •    Proven ability to coach, develop, and lead teams. •    Result-oriented with excellent communication skills in Dutch and English. •    Additional certifications (e.g., Pressure API standards, Certified Reliability or Maintenance Professional) are beneficial. Other Information: If you are interested and want to apply, please submit your application via the apply button below and contact me.  

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 Voedingsmiddelentechnologie, Food & Quality Management, Levensmiddelentechnologie of vergelijkbaar Ervaring binnen Quality Assurance of Quality Engineering in de voedingsmiddelenindustrie Diepgaande kennis van IFS, HACCP, RSPO, Beter Leven en kwaliteitsmanagementsystemen Ervaring met audits, procesverbetering en kwaliteitsborging Ervaring met ERP-systemen en QA-software Sterke analytische vaardigheden en ervaring met root cause analyses Goede communicatieve vaardigheden en stakeholdermanagement Goede beheersing van de Nederlandse en Engelse taal

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 and commitment to quality. - Comfortable working in a regulated environment and following procedures. - Good English communication skills. - Team player with a proactive and continuous improvement mindset. - Experience with SAP and/or MES is an advantage but not required. Other Information If you are interested and want to apply, please submit your application via the apply button below and contact me.  

Company: A global leader in pharmaceutical and medical device manufacturing, focused on high quality production, innovation, and regulatory compliance. The organization operates in a highly regulated environment with a strong emphasis on automation, safety, and continuous improvement. Job Description: The Senior Equipment Engineer plays a key role in leading and executing technical projects that support manufacturing operations, particularly in device assembly, inspection, labeling, and packaging. This position is responsible for managing the full lifecycle of equipment, from design and installation to optimization and maintenance. You will act as the technical lead within project teams, collaborating with internal stakeholders and external vendors to ensure equipment performance, reliability, and compliance with regulatory standards. Responsibilities: - Lead technical execution for assigned equipment or process areas within capital and operational projects - Serve as the main technical liaison between internal teams and equipment vendors - Translate user and process requirements into detailed technical specifications - Collaborate with project managers on timelines, risks, and deliverables - Develop engineering documentation including URS, FDS, HDS, and design reviews - Coordinate detailed engineering activities and ensure compliance with requirements - Conduct equipment characterization and performance testing through controlled experiments - Support factory acceptance testing and site acceptance testing activities - Oversee installation, commissioning, and validation of equipment systems - Troubleshoot equipment failures and implement corrective actions - Drive continuous improvement initiatives to enhance performance, safety, and efficiency - Support root cause investigations and cross functional problem solving - Ensure compliance with good manufacturing practices and internal procedures - Promote a safe working environment aligned with health and safety standards Requirements: - Bachelor’s degree or higher in Mechanical Engineering or a related field - Minimum 6 years of relevant experience, with at least 4 years in manufacturing or operations - Experience in pharmaceutical, medical device, or automated assembly environments - Hands on experience with commissioning and equipment validation - Strong knowledge of equipment design, installation, and maintenance processes - Experience working in regulated environments such as GMP, OSHA, or EPA - Strong project management and stakeholder communication skills - Ability to create detailed engineering documentation and specifications - Proficiency in Microsoft Office tools - Fluent in English, both spoken and written - Willingness to occasionally work outside standard office hours Other Information: - Works closely with cross functional engineering, quality, and operations teams - Involves interaction with external equipment vendors and suppliers - May require flexibility in working hours depending on project needs

Over het Bedrijf Deze internationale zuivelorganisatie levert hoogwaardige ingrediënten aan klanten over de hele wereld en opereert binnen een complexe internationale supply chain. De organisatie combineert commerciële groei met operationele excellentie en werkt nauw samen tussen Sales, Demand Planning, Productie en Supply Chain om optimale klanttevredenheid en leverbetrouwbaarheid te realiseren. Rolomschrijving Als Demand & Goods Manager ben je de verbindende schakel tussen Sales, Demand Planning en Supply Chain. Je vertaalt commerciële forecasts naar een geïntegreerd supply chain plan en zorgt voor een optimale balans tussen klantvraag, productiecapaciteit en voorraad. Door middel van analyses, scenario's en forecasting ondersteun je strategische besluitvorming en draag je bij aan een efficiënte en toekomstbestendige S&OP-organisatie. Belangrijkste Verantwoordelijkheden Vertalen van commerciële forecasts naar geïntegreerde supply chain- en S&OP-plannen Opstellen van scenarioanalyses voor goederenstromen, voorraadoptimalisatie en serviceverbetering Fungeren als schakel tussen Sales, Demand Planning, Productie en Supply Chain Beheren en reduceren van obsolete en restricted voorraad met minimale financiële impact Ondersteunen van phase-in en phase-out trajecten in samenwerking met Innovation en Commercial Verbeteren van demand planning-, forecasting- en customer collaboration-processen Analyseren van KPI's en rapporteren via Power BI, OMP en andere planningssystemen Bijdragen aan de verdere ontwikkeling richting Integrated Business Planning (IBP) Vereisten Ruime ervaring binnen Demand Planning, Supply Planning, S&OP of Supply Chain Planning Goede kennis van zowel commerciële forecasting als productie- en supply chain-processen Ervaring met S&OP-processen, forecasting en voorraadbeheer Ervaring met OMP, Power BI, SAP of vergelijkbare planningssystemen Sterke analytische vaardigheden en het vermogen om data om te zetten in concrete beslissingen Uitstekende communicatieve vaardigheden en stakeholdermanagement Ervaring binnen de zuivel-, ingrediënten-, chemische-, food- of FMCG-sector is een sterke pré Goede beheersing van zowel de Nederlandse als Engelse taal

About the Company This global pharmaceutical manufacturer produces life-changing medicines using advanced manufacturing technologies within a highly regulated GMP environment. The organization is committed to quality, operational excellence, and continuous improvement, offering employees the opportunity to work with modern manufacturing systems while contributing to the delivery of products that improve patients' lives. Role Description As a Process Technician, you will be responsible for operating and supporting semi-automated and manual packaging processes in a GMP manufacturing environment. You will ensure production activities are executed safely, accurately, and in compliance with quality standards while performing documentation, inspections, and routine equipment operations. Working closely with Production, Quality, and Maintenance, you will help maintain reliable production processes and contribute to continuous improvement initiatives. Key Responsibilities Operate semi-automated and manual packaging equipment in accordance with GMP procedures Perform packaging, labelling, inspection, and verification activities to ensure product quality Complete production documentation, batch records, and electronic data entry accurately Carry out basic equipment setup, changeovers, and minor troubleshooting activities Monitor production performance and escalate technical or quality issues when required Perform quality checks and ensure compliance with SOPs, GMP, and documentation standards Support continuous improvement initiatives to enhance safety, quality, and efficiency Collaborate with Production, Quality, Maintenance, and Engineering teams to maintain smooth operations Requirements Experience as a Production Operator, Technical Operator, Process Operator, Packaging Operator, or similar role within manufacturing Experience working in a GMP, ISO, or other regulated production environment Hands-on experience operating production or packaging equipment Strong attention to detail with experience completing production documentation and batch records Experience with SAP, MES, or other manufacturing systems is highly desirable Basic troubleshooting skills and the ability to perform machine adjustments and changeovers Continuous Improvement mindset with exposure to Lean, 5S, or Kaizen principles Strong communication skills and the ability to follow structured procedures Willingness to work in a 3-shift environment and overtime when required Fluent in English

About the Company This global pharmaceutical manufacturer is dedicated to producing life-changing medicines through advanced manufacturing technologies and operational excellence. Operating in a highly regulated environment, the organization invests heavily in automation, continuous improvement, and employee development to ensure the highest standards of quality, safety, and efficiency. Role Description As a Manufacturing Process Technician, you will act as the technical expert on highly automated production lines, ensuring equipment operates safely, efficiently, and reliably. You will take ownership of troubleshooting complex process issues, performing root cause investigations, optimizing line performance, and supporting continuous improvement initiatives. Working closely with Production, Engineering, Maintenance, and Quality teams, you will play a key role in maximizing equipment performance while maintaining compliance with GMP standards. Key Responsibilities Operate, monitor, and optimize highly automated manufacturing equipment and production lines Troubleshoot technical issues, perform root cause analyses, and implement sustainable corrective actions Lead continuous improvement initiatives focused on efficiency, reliability, and waste reduction Monitor production performance using KPIs and identify opportunities to improve OEE and process stability Support machine changeovers, equipment settings, and process optimization activities Collaborate with Maintenance, Engineering, and Quality to resolve technical and operational challenges Maintain accurate production documentation and ensure compliance with GMP and quality requirements Act as the technical expert on the production line while coaching and supporting fellow operators Requirements Minimum 2 years of experience within automated manufacturing or process technology (senior profiles also considered) Hands-on experience with highly automated production equipment and manufacturing processes Strong troubleshooting and Root Cause Analysis (RCA) skills (e.g. 5 Why, Fishbone, Kaizen, TPM) Experience with Lean Manufacturing, Continuous Improvement, OEE, or process optimization Technical background in Process Technology, Mechatronics, Mechanical Engineering, Manufacturing, or similar Experience with SAP, MES, or other manufacturing systems is highly desirable Experience within pharmaceutical, medical device, food, FMCG, chemical, automotive, or other highly automated manufacturing environments Willingness to work in a 3-shift schedule with the possibility of transitioning to a 5-shift operation Strong analytical, problem-solving, and communication skills Fluent in English; GMP experience is an advantage but not essential

Company Our client is a leading organization dedicated to ensuring the highest standards in food safety, quality, and sustainability. They are committed to continuous improvement and maintaining compliance with industry regulations and certifications. Role Description We are seeking an experienced Quality Assurance Specialist to ensure compliance with food safety, quality, and environmental standards across our production operations. The successful candidate will be responsible for maintaining and improving the Quality Management System (QMS), leading audits, driving continuous improvement initiatives, and supporting production teams in achieving the highest quality standards.   Responsibilities - Ensure compliance with food safety, quality, environmental regulations, and internal company standards. - Maintain, monitor, and continuously improve the Quality Management System (QMS) and process control systems. - Lead and participate in internal and external audits, including preparation, execution, corrective actions, and follow-up. - Ensure compliance with certification standards such as IFS, HACCP, RSPO, and Beter Leven, including timely renewals. - Act as the primary quality advisor to the QE Manager and Production team on quality and process-related matters. - Initiate and lead continuous improvement projects focused on quality enhancement and process optimization. - Conduct root cause analyses for non-conformities, customer complaints, and production deviations, implementing corrective and preventive actions. - Monitor and manage production quality issues, product holds, and process deviations to minimize risks. - Collaborate with cross-functional teams to improve operational performance and product quality. - Coordinate with external laboratories, certification bodies, pest control providers, and suppliers. - Prepare, analyze, and present KPIs, quality reports, and trend analyses to management. - Organize and deliver quality and food safety training sessions and toolbox meetings. Requirements - Bachelor's degree (HBO) in Food Technology, Food Science, Food & Quality Management, or a related field. - Strong knowledge of food safety and quality standards, including IFS, HACCP, RSPO, and Beter Leven. - Experience with quality management systems, audit planning, and process improvement. - Proficiency in ERP systems and Quality Assurance (QA) software. - Excellent analytical, problem-solving, and organizational skills. - Strong communication and stakeholder management abilities. - Fluency in Dutch and English, both written and spoken. Other Information If you are interested and want to apply, please submit your application via the apply button below and contact me.