Cell Therapy Manufacturing Technician, Hoofddorp, Noord-Holland

Company A reputable company committed to maintaining high standards of food safety and quality within the food manufacturing industry. The organization values proactive teamwork, continuous improvement, and a strong focus on food safety protocols. Job Description We are seeking a dedicated QA Coordinator to join our enthusiastic quality team. This senior role involves supporting and ensuring the ongoing quality of our products and processes across our factories in Venlo and Belfeld. The successful candidate will serve as a key partner to the QA Manager, driving quality initiatives and fostering a culture of food safety and excellence. Responsibilities - Maintain and update quality procedures and the quality handbook in collaboration with the QE Manager. - Handle internal and external complaints related to production, ensuring timely follow-up. - Manage and follow up on product holds and resolve quality issues across production processes. - Conduct process and product inspections to ensure compliance with quality standards. - Organize and participate in internal audits and hygiene inspections. - Prepare and review product specifications and documentation. - Follow the annual Quality & Environment plan and ensure tasks are completed. - Act as a liaison between departments to promote awareness and adherence to food safety and quality protocols. - Lead by example to motivate production staff and raise awareness around food safety practices. Requirements - Minimum MBO level education, preferably with a degree in Food Technology. - Hands-on experience in quality assurance within the food industry. - Proactive attitude with the ability to solve problems independently. - Strong communication skills in both Dutch and English. - Good knowledge of Word and Excel. - Experience in a senior QA role is preferred, with a focus on continuous improvement and leadership. Other Information If you are interested and want to apply, please submit your application via the apply button below and contact me.  

Job Description We are seeking a motivated Advanced Therapies Specialist to support the production of clinical and commercial cell therapy products in a GMP-regulated aseptic manufacturing environment. In this role, you will collaborate with cross-functional teams to ensure safe, compliant, and efficient manufacturing while maintaining the highest quality standards. Key Responsibilities -Perform manufacturing activities, including aseptic processing, batch documentation, and sample handling. -Prepare growth media in cleanroom environments and carry out material decontamination procedures. -Complete and review batch records to ensure GMP compliance and accurate documentation. -Transfer samples for quality control analysis and perform cryopreservation of excess cells and finished products. -Assist with troubleshooting manufacturing equipment and recommend process improvements. -Participate in continuous improvement and change control initiatives. -Maintain cleanroom standards and ensure manufacturing workstations remain organized and compliant. -Work a rotating shift schedule, including mornings, evenings, and weekends, based on production Requirements -MLO, MBO, or HBO qualification (MBO Level+ or higher) in Life Sciences or a related discipline. -Experience working in a cGMP-regulated pharmaceutical, biotechnology, or similar manufacturing environment. -Understanding of biopharmaceutical manufacturing processes. -Practical experience with aseptic techniques and handling blood-derived products. -Knowledge of Vapro A/B or LITOP A/B is considered an advantage. -Proficiency in Microsoft Office applications, particularly Word and Excel, with basic data analysis skills. -Ability to follow SOPs accurately, work independently, and perform effectively in a dynamic manufacturing environment. -Good verbal and written communication skills in English. Dutch language skills are not required. -Willingness to receive a Hepatitis B vaccination if not already vaccinated. Additional Information Interested in this opportunity? Click the Apply button to submit your application or contact me directly for more information.

Company Overview: We are an international healthcare manufacturing organization operating within a highly regulated GMP environment. Using advanced automation and strong quality standards, we ensure safe, compliant, and efficient production processes supporting patients worldwide. Job Description: We are seeking a Senior Technical Operator – Automated Lines to support automated production operations within a GMP-regulated manufacturing environment. In this role, you will act as a technical expert on the production floor, ensuring stable and efficient production processes while supporting troubleshooting, process improvements, and operational excellence across automated manufacturing lines. You will work closely with production, maintenance, engineering, and quality teams to maintain high production and compliance standards. Key Responsibilities: • Operate and monitor automated production equipment and manufacturing lines • Perform line set-ups, changeovers, cleaning, and line clearances • Execute advanced troubleshooting and Root Cause Analysis (RCA / 5-Why) • Act as Subject Matter Expert (SME) and support technical escalations • Perform minor equipment adjustments and first-line maintenance activities • Monitor and document production data within SAP and/or MES systems • Support deviation handling and technical investigations • Drive Lean Manufacturing and Continuous Improvement initiatives • Coach and support operators and team members on the production floor • Ensure GMP, safety, and quality compliance at all times Requirements: • MBO+ or equivalent technical education • Experience within automated manufacturing or production environments • Strong troubleshooting and analytical skills • Experience working within GMP or other regulated production environments • Familiarity with SAP and/or MES systems • Knowledge of Lean Manufacturing and Continuous Improvement methodologies • Experience as SME, senior operator, trainer, or technical lead is an advantage • Strong communication, coordination, and problem-solving skills • Good communication skills in English; Dutch is considered an advantage • Willingness to work in shifts Additional Information: • This role currently operates in a 3-shift rotation and will transition to a 5-shift schedule from 2027 onwards • Opportunity to work in a highly automated and technically advanced manufacturing environment If you are interested in this opportunity and would like to apply, please submit your application or contact us directly for more information.

The Company Our client is a leading global food and nutrition company dedicated to improving health through high-quality nutritional products. Driven by innovation, sustainability, and customer excellence, the organization partners with healthcare providers, wholesalers, and retailers to deliver trusted nutrition solutions across the Netherlands. Role Description We are seeking a proactive and detail-oriented Account Support Specialist to join the Contract & Tender Management team. You will support commercial operations by managing pricing, product administration, and customer agreements while working closely with Sales, Marketing, Supply Chain, Business Intelligence, and Master Data teams. Key Responsibilities Maintain master and customer-specific price lists, assortments, and article code changes. Manage commercial pricing agreements and SAP workflows. Validate SAP pricing conditions and resolve pricing discrepancies. Support New Product Introductions (NPI). Communicate product, pricing, and stock updates to wholesale partners. Process monthly indirect sales data with the Business Intelligence team. Maintain customer master data and support process improvements. Key Requirements MBO/HBO degree in Business Administration, Commercial Economics, Supply Chain, or related field. Minimum 3 years' experience in Commercial Support, Sales Support, Customer Service, or Account Administration. Fluent in Dutch and English. SAP experience preferred. Strong Excel, organizational, and communication skills. Customer-focused, proactive, and detail-oriented. Other Information Are you interested in this or another role? click the apply button below and I will contact you as soon as possible

The Company The client is a Dutch/Belgian food manufacturing company focused on frozen snacks, meal components, and private-label food products across Europe. Role Description As a Senior QA Officer, you will play a key role within a close-knit quality team of four, supporting the maintenance and continuous improvement of quality standards across the production sites in Venlo and Belfeld. This is a senior-level position where you will act as the right-hand to the QA (QE) Manager, contributing both strategically and operationally to quality assurance activities. You will work in a fast-paced, dynamic environment where no two days are the same, ensuring that quality and food safety remain central to all processes. Acting as a link between multiple departments, you will help embed a strong quality culture throughout the organization. Responsibilities Maintaining and updating quality systems and the quality handbook in collaboration with the QE Manager. Monitoring and handling internal and external complaints related to production. Managing product holds and following up on quality-related process deviations. Conducting inspections on products and production processes. Organizing and executing internal audits and hygiene checks. Preparing, reviewing, and maintaining product specifications and documentation. Executing tasks aligned with the annual Quality & Environment plan. Ensuring quality standards are upheld across raw materials, finished goods, and production processes. Acting as a point of contact between departments, promoting cross-functional collaboration. Leading by example on the production floor and actively promote awareness of food safety and quality standards. Requirements Minimum MBO level of education and thinking, preferably with a completed degree in Food Technology. Proven experience in a similar QA role, ideally within the food industry. Proactive, hands-on mentality with strong problem-solving skills and the ability to work independently. Strong communication skills, with the ability to influence and engage stakeholders at all levels. Solid working knowledge of Microsoft Word and Excel. Fluency in both Dutch and English. Senior mindset with the ability to support and act as a trusted deputy to the QA Manager. Other information   Apply to our vacancy for more information. Looking forward to getting in touch!  

Company: Our client is a leading global manufacturer of advanced equipment dedicated to the food processing industry. Their innovative machinery is used by top food producers worldwide. The company values modern technology, skilled craftsmanship, and a professional, team-oriented work environment focused on quality and continuous improvement. Job Description: We are looking for a Mechanical Assembly Technician to join our client’s team. In this role, you will assemble mechanical and mechatronic machines from individual components, ensuring each system is built to the highest standards, thoroughly tested, and ready for delivery. This position is perfect for someone who enjoys practical work, problem-solving, and working with complex machinery. Responsibilities: •    Assemble mechanical and mechatronic modules according to technical drawings and instructions. •    Build complete machines based on customer specifications. •    Conduct inspections, adjustments, and functional testing during assembly. •    Identify and report technical issues or suggestions for improvements. •    Ensure all products meet quality and safety standards. •    Work efficiently to meet production deadlines. •    Maintain a clean and safe working environment. •    Collaborate effectively with colleagues and production teams. Requirements: •    Technical education in mechanical engineering, mechatronics, or a related field. •    Preferably some experience in assembling mechanical or machinery components. •    Ability to read and interpret technical drawings. •    Good mechanical insight and problem-solving skills. •    Detail-oriented and quality-focused. •    Capable of working independently and as part of a team. •    Basic English communication skills are an advantage. 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 leading global organization in the pharmaceutical and life sciences sector, focused on innovation, research, development, and manufacturing. The organization manages a significant portfolio of capital investment projects and supports multiple operational and research facilities through dedicated engineering and project management teams. About the Role The Project Administrator supports the Site Engineering department by providing administrative, secretarial, and project coordination support. This position plays a crucial role in ensuring efficient project execution, supporting engineering teams, maintaining project systems, and driving process improvements related to administration and project management activities. Responsibilities - Provide administrative and secretarial support to the Site Engineering  department and project teams - Create purchase orders and process invoices within SAP SRM - Register and manage notifications within SAP PM - Serve as key user for SAP SRM and SAP PM and support colleagues with system usage - Coordinate onboarding and offboarding activities for new employees - Support recruitment administration and system related job creation - Manage agendas and scheduling support for leadership - Maintain employee training records and learning systems - Coordinate required training activities for engineering staff - Update performance boards and process improvement actions - Manage office supplies and coordinate office equipment maintenance - Maintain department intranet content and project information - Support the initiation of new projects within internal systems - Assist with internal communication regarding projects and department activities - Prepare meeting agendas, reports, meeting minutes, and departmental communications - Participate in administrative process improvement initiatives using Lean methodologies Requirements -Minimum 5 years of administrative experience within a project-based environment -Ideally, speak Dutch fluently. -Previous experience in project support or coordination is a plus. -organizational and communication skills. -Ability to work independently and as part of a team. -Willingness to support and follow directions from senior staff. 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 global leader in innovative chemical solutions committed to creating a more sustainable and environmentally friendly future. They operate across multiple regions, focusing on advanced technology and responsible business practices to deliver high-quality products to their customers. Role Description: The Regional Cost & Asset Management Specialist is responsible for overseeing project financials and fixed asset management, primarily supporting capital projects and ensuring accurate asset records. Based in Dordrecht, Netherlands, this role involves working closely with project teams to control costs, manage financial reporting, and coordinate fixed asset activities across multiple sites in the region. Responsibilities: -Prepare and review monthly project financial reports, including capital expenditures, field costs, equipment, and contingencies. -Lead financial reviews for major and minor projects, analyzing progress and deviations. -Maintain and process change logs and document approvals aligned with company policies. -Develop expenditure forecasts, considering currency fluctuations and project scope changes. -Support project teams with cost transfer requests and manage financial documentation for audits. -Oversee the fixed asset process, ensuring proper tagging, disposal, transfer, and record keeping. -Coordinate physical asset verifications and communicate with relevant internal and third-party teams. -Serve as a link to the Asset Management group for asset sales or redeployment. Assist in the Capex reconciliation process, supporting internal and external audits. Requirements: -Bachelor’s degree or equivalent work experience. -Proven ability to manage multiple projects and adapt quickly. -Strong organizational and communication skills, with the ability to influence at all levels. -Fluency in English; Dutch language skills are a plus. -Demonstrated experience in cost control for capital projects, ideally in the chemical or related industry, with over 10 years of relevant experience. -Knowledge of multi-currency cost management is preferred. -Technical or engineering background is advantageous. 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 leading organization in the biotechnology and advanced cell therapy sector focused on developing and manufacturing innovative treatments. The company operates in a highly regulated GMP environment with a strong emphasis on quality, patient safety, process excellence, and continuous improvement. Role Description This position supports the manufacturing of clinical and commercial cell therapy products within a GMP regulated environment. Successful candidates will be assigned to either the Production Team or Production Support Team after completing initial training requirements. The role requires hands on manufacturing activities, strict adherence to SOPs and GMP standards, and close collaboration with multiple operational and quality functions. Responsibilities - Perform apheresis accession and transfer to manufacturing areas - Complete batch records according to SOPs and GMP requirements - Support batch documentation review for product release activities - Supply manufacturing suites with required materials and components - Transfer batch records and documentation into cleanroom environments - Conduct final product visual inspections - Perform cryopreservation of excess cells and final product - Submit manufacturing samples to Quality Control - Manufacture clinical and commercial products in Grade A and Grade B cleanroom environments - Complete manufacturing batch records accurately and compliantly - Draft and revise batch records, SOPs, and work instructions - Support deviation investigations and corrective actions - Participate in change management implementation - Troubleshoot processing and equipment related issues - Collaborate with Production Support, Product Sciences, Materials Management, Quality Assurance, and Quality Control teams Requirements - MLO, MBO, or HBO qualification with a Life Sciences background - Experience working within a pharmaceutical, biotechnology, or related manufacturing environment - Proven knowledge of biotechnology or pharmaceutical manufacturing processes - Strong understanding of cGMP regulations and compliance requirements - Experience working within controlled cleanroom environments - Ability to work aseptically and follow strict gowning procedures - Strong troubleshooting and problem solving abilities Other Information If you are interested and want to apply, please submit your application via the apply button below and contact me.

Company A leading producer of medical devices, our client operates a state-of-the-art manufacturing facility dedicated to healthcare innovation. They prioritize quality, safety, and compliance, creating a dynamic environment where operational excellence drives their success. Role Description We are seeking a Facilities Engineer to oversee and optimize the daily maintenance and utility systems at their Leiden site. This hands-on role is vital for ensuring the smooth running of manufacturing facilities, maintaining safety and environmental standards, and supporting continuous improvement initiatives. Responsibilities - Lead daily facilities and utilities operations, ensuring safe, efficient, and compliant performance. - Drive EHS compliance, safety initiatives, and environmental improvement plans. - Manage preventive maintenance for utilities, manufacturing, and laboratory equipment. - Lead capital facilities projects, including planning, budgeting, contractor, and project management. - Ensure all engineering, installation, and maintenance activities comply with GMP, EHS, and regulatory standards. - Coach and support engineering teams, promoting continuous improvement and best practices. - Identify and implement energy-saving initiatives to improve efficiency and reduce costs. - Support audits, inspections, and risk management, ensuring operational and regulatory compliance. Requirements - Bachelor's degree in Engineering or a related technical discipline. - 5–7 years of experience in Facilities, Engineering, or Maintenance within a GMP/regulated environment. - Strong knowledge of GMP, EHS, Quality Systems, Utilities, and Maintenance. - Proven experience in project management, contractor supervision, and performance monitoring. - Strong troubleshooting skills for utilities and mechanical systems. - Excellent communication skills in English. - MSc, MBA, or PE certification is an advantage. - Proactive, service-oriented, and able to manage multiple priorities in a dynamic environment. Other Information If you are interested and want to apply, please submit your application via the apply button below and contact me.