Quality Engineer, Oudkarspel, Noord-Holland

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.  

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 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.

The Company  Our client is a leading multinational dairy and nutrition company headquartered in the Netherlands, serving customers in over 100 countries. The organization specializes in high-quality dairy ingredients, consumer products, and nutritional solutions, with a strong focus on innovation, sustainability, and supply chain excellence. Role  Description We are recruiting a Supply Planning Manager to join the Planning & Delivery team for an  5-month maternity cover. The successful candidate will bridge the gap between production, supply chain, and sales/demand teams. This role requires a proactive, results-driven professional with a strong understanding of demand planning and supply chain processes, capable of guiding the team towards optimized business operations and demand accuracy. Responsibilities -Coordinate demand consolidation from a supply chain perspective, ensuring a smooth S&OP process aligned with market demands. -Develop comprehensive views and scenarios for goods movement to support end-to-end supply chain optimization and S&OP decision-making. -Integrate commercial priorities into the S&OP plan, ensuring alignment with market realities. -Collaborate with the Innovation team to implement phased product introductions and discontinuations within the S&OP framework. -Manage obsolete and restricted stock inventory, working with Sales to analyze and minimize financial impact. -Liaise with the Global Demand Manager to prioritize product allocation based on demand patterns. -Enhance demand management and sales forecasting by partnering with sales regions and customers, driving continuous improvement programs. -Support the transition towards Integrated Business Planning, moving from volume-based to financially driven business models. Act as the key link between sales, demand, and supply chain teams, ensuring smooth communication and process integration. Requirements -Relevant experience in demand planning or supply chain management preferred. -Experience in the ingredients or dairy industry preferred. -Excellent communication skills in English and Dutch. -University degree, preferably in Supply Chain, Business, or a related field. -Experience in a cross-functional or bridging role between production and sales is highly desirable. Ability to handle operational tasks while maintaining a strategic overview. -Proven experience with collaborative projects and process improvement initiatives. Other Information -If you are interested and want to apply, please submit your application via the apply button below and contact me.  

The Company: A large international organisation in the Fast-Moving Consumer Goods (FMCG) sector, focused on optimising pricing and revenue strategies. The company leverages data and innovation to identify market opportunities and stay ahead of the competition.. Role Description: We are seeking a proactive and detail-oriented Innovation Laboratory Technician to support our product development and quality assurance efforts. This role involves working closely with the R&D team to create prototypes, manage testing processes, and ensure product quality in a fast-paced, innovative environment. Responsibilities: -Assist in developing rapid prototypes for new products and packaging concepts in line with project timelines. -Support product and packaging developers in crafting samples within the development kitchen and pilot plant. -Ensure all prototypes comply with global standards, including good manufacturing practices (GMP), HACCP, and quality management protocols. -Conduct lab tests and trials during product development phases. -Collaborate with external partners for nutrition analysis and other testing services. -Lead shelf life studies and coordinate domestic and international logistics for sample sharing. Requirements: -Bachelor's degree in Food Science, Nutrition, or a related technical field. -Fluent in English; Dutch language skills are a plus. -Some experience working in a pilot plant or product development environment preferred. -Strong organizational skills and ability to work independently. -Good communication skills, both verbal and written. -Ability to walk throughout the plant, work on multiple levels, stand for long periods, and lift up to 25kg. Other Information: If you are interested and want to apply, please submit your application via the apply button below and contact me.

Company Overview: Our client is a well-established, internationally active company rooted in Dutch heritage. They offer a dynamic and collaborative work environment focused on innovation and growth within the supply chain and ingredients markets. The organization values long-term impact, professional development, and fostering a friendly, informal workplace culture. Job Description We are seeking a Supply Chain & Demand Coordination Specialist to join the Demand & Goods team. In this vital role, you will act as a bridge between production, supply chain, and sales, ensuring accurate forecasting and smooth coordination across all functions. You will support demand planning, optimize product availability, and contribute to the company’s supply chain excellence during an exciting growth phase. Responsibilities -Manage demand consolidation from a supply chain perspective to support demand-driven sales and operations planning (S&OP). -Develop comprehensive views and scenarios for goods movement to enable end-to-end (E2E) supply chain optimization and aid S&OP decision-making. -Ensure that market and commercial priorities are properly integrated into the S&OP plan. -Collaborate with the Innovation team on phase-in and phase-out planning for products, supporting seamless product transitions. -Oversee inventory management concerning obsolete and restricted stock—report, analyze, and work with sales to minimize financial impact. -Coordinate with the Global Demand Manager to set priorities and manage product allocations effectively. -Improve demand management and sales forecasting processes by working closely with regional sales teams and customers. -Drive initiatives to evolve the business from a volume-focused model to a financially driven, fully optimized IBP process. -Support operational and process improvements, ensuring smooth communication between demand management and supply teams. Requirements -Significant experience in demand planning, supply chain, or a related field, with knowledge of the dairy or ingredients industry being a plus. -Strong understanding of demand and sales forecasting processes, supply chain dynamics, and inventory management. -Proven ability to work as a link between production, supply chain, and sales teams, with some   leadership or coordination experience. -Fluent in English and Dutch. -A relevant master’s degree is preferred for quick onboarding and success in the role. -Comfortable working in a fast-paced environment with a strategic mindset and operational awareness. -Experience in chemical or ingredients industries is also relevant. 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

Company: A leading organization in the food innovation industry dedicated to developing and testing new products and packaging solutions. The company values creativity, quality, and sustainability, working globally to shape the future of food. Job Description: We are seeking a proactive and detail-oriented Innovation R&D Innovation Technician  to support the company's product development activities. This role involves working closely with the R&D team to create prototypes, conduct trials, and manage samples, all while ensuring strict adherence to quality standards. Responsibilities: - Develop rapid prototypes of products and packaging to assist in launching new innovations and concepts. - Support product and packaging developers by preparing samples in the development kitchen and pilot plant. - Ensure all prototypes meet global standards, including good manufacturing practices, HACCP, and quality management protocols. - Assist with pilot scale trials alongside the pilot plant team. - Conduct laboratory tests for products during development phases. - Coordinate with external partners for nutrition analysis and other testing. - Lead and oversee shelf-life studies. - Manage logistics for international sample sharing and benchmarking activities. - Establish and maintain a global network for product ordering, tastings, and stakeholder engagement. - Organize quarterly competitor tastings and support global R&D meetings with product showcases. Requirements: - BSc in Food Science, Food Technology, or a related field. - Excellent verbal and written communication skills in English; Dutch is a plus. - Some experience working in a pilot plant environment is preferred. - Ability to work independently, manage time efficiently, and take initiative. - Strong teamwork skills. - Understanding of quality standards and manufacturing principles. - Physical ability to walk around the plant, work on multiple levels, stand for prolonged periods, and lift up to 25kg. - Willingness to travel daily to the Oud-Beijerland plant. - Ambition to grow within the product development field. Other Information: If you are interested and want to apply, please submit your application via the apply button below and contact me.  

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 An international biotechnology organization active in cell therapy for oncology treatments. The company operates a highly regulated GMP manufacturing facility in Hoofddorp, closely connected to global hospital networks to process patient-derived cellular products for clinical and commercial use. Role Description As a Cell Therapy Specialist, you will support the manufacturing of autologous cell therapy products in a GMP cleanroom environment. After completing the initial training program, you will be assigned to either the Production Team (PT) or the Production Support Team (PST). This is a hands-on, operational role with a strong focus on aseptic processing, documentation accuracy, and compliance. The position follows a two-shift system, including weekends, and requires working in full gowning within Grade A/B/C cleanroom environments. Key Responsibilities Production Support Team (PST) Perform apheresis material accessioning and transfer to manufacturing areas Prepare growth media in Grade C cleanroom environments Supply manufacturing suites with required materials and components Perform material decontamination prior to cleanroom entry Manage batch documentation flow to and from cleanroom nests Support batch record review to ensure timely release Perform visual inspection of final product Cryopreserve excess cells and final product Transfer and submit samples to QC for testing Production Team (PT) Execute clinical and commercial manufacturing steps in Grade A/B cleanrooms according to batch records and SOPs Support GMP runs in collaboration with PST, Product Sciences, QA, QC, and Material Management Draft and revise batch records, SOPs, and work instructions Support deviation investigations and change management activities Troubleshoot process- and equipment-related issues Ensure strict compliance with cGMP requirements and accurate documentation Maintain cleanroom nests in an optimal state Identify opportunities for process improvements to enhance quality and efficiency Working Conditions Two-shift system: Morning: 07:00 – 15:00 Evening: 16:30 – 23:30 / 00:00 Weekend shifts included On-site role Full cleanroom gowning required Training period of approximately 2 months (day shift) Working with blood-derived biological materials (hepatitis B vaccination recommended) Requirements Vocational / technical education (MBO level or equivalent); maximum completed level: BSc Experience in a GMP-regulated manufacturing environment (biotech, pharma, medical devices) Knowledge of pharmaceutical or biotechnology manufacturing processes Comfortable working in aseptic cleanroom environments Strong attention to detail and ability to strictly follow SOPs Willingness to work shift schedules, including weekends Professional working proficiency in English