Global HR Service Delivery Specialist, Amersfoort, Utrecht

The Company Our client is a global leader in health technology, developing innovative solutions across medical imaging, patient monitoring, diagnosis, and personal health. With a strong focus on research and innovation, the organization combines advanced technology, engineering, and data-driven solutions to improve healthcare outcomes worldwide. Job Description As an Electronics Design Engineer, you will be responsible for developing, testing, and improving electronic hardware and non-graphical user interface components for advanced medical systems. The role involves evaluating prototypes, conducting functional and feasibility testing, troubleshooting electronic subsystems, and collaborating with cross-functional engineering teams and external suppliers to ensure reliable product performance. Responsibilities - Provide technical expertise in non-graphical user interface hardware, components and configurations. - Define technical requirements for subsystems and units, translating application performance into design improvements. - Evaluate supplier prototypes and recommend improvements where needed. - Plan and perform feasibility and functional testing. - Build test setups, collect data and analyse test results. - Investigate technical issues and assess the performance and reliability of components and subsystems. - Perform systematic risk and safety assessments. - Take ownership of assigned units throughout engineering projects. Requirements - A Bachelor’s or Master’s degree in Electrical Engineering, Electronic Engineering or a comparable discipline. - At least five years of relevant engineering experience in the consumer or professional electronics industry. - Proven R&D experience in product design, development and maintenance. - Experience working with external vendors and suppliers. - A hands-on approach to laboratory investigations, testing and troubleshooting. - Strong analytical, simulation and conceptual thinking skills. - Good written and verbal communication skills in English. Other Information Apply to our vacancy for more information. We look forward to hearing from you!

Company  A large, modern food manufacturing site producing high volumes for an international market. The environment is fast-paced and highly automated, with a wide variety of process and packaging equipment. The maintenance organization focuses on safety, reliability, and minimizing downtime through strong planning and coordination. Job Description  We are looking for a Maintenance Scheduling Coordinator to plan and coordinate preventive and corrective maintenance activities across multiple production lines. The Maintenance Scheduling Coordinator ensures that planned line stops are used effectively, work orders are well prepared, and the right technicians are assigned at the right time—helping keep production running smoothly with minimal disruption. Responsibilities  - Build and manage maintenance schedules for planned line stops, balancing priorities and operational needs. - Assign prepared work orders to technicians, matching job complexity with the right technical skillsets. - Prepare, plan, and allocate work orders using systems such as SAP PM and Microsoft Excel. - Align planned maintenance with production planning and ensure weekly maintenance plans are confirmed in advance. - Replan quickly when unexpected issues occur, coordinating with maintenance leadership and communicating changes to relevant teams. - Support resource planning by coordinating capacity and availability with team leaders to ensure coverage during line stops. - Collaborate closely with other maintenance planners and work preparers across mechanical, electrical/instrumentation, and utilities. - Contribute to continuous improvement by identifying ways to make planning and execution more efficient. Requirements   - Completed vocational education (MBO level 4 or similar). - Proven experience in planning/scheduling (maintenance planning experience is a strong advantage). - Strong coordination skills and the ability to work smoothly across multiple departments. - Accurate, punctual, proactive, and a strong team player. - Comfortable working with Microsoft Office (especially Excel); experience with SAP PM is a strong plus. - Fluency in both Dutch and English (written and spoken). - Affinity with technical environments (a technical background is not required). - High sense of responsibility regarding safety and quality/food safety. Other Information This position is based on-site in Veghel (Netherlands), within a large maintenance organization supporting a complex production environment. If you are interested and want to apply, please submit your application via the apply button below and contact me.

Company Our client operates a large, modern manufacturing site producing high-volume consumer goods for an international market. The environment is fast-paced and highly regulated, with a strong focus on safety, quality, and continuous improvement. The technical landscape is diverse, covering production, packaging, and conveying systems. Job Description For this site, we are looking for a Maintenance Planning Coordinator who will coordinate preventive and corrective maintenance planning to support reliable production. The Maintenance Planning Coordinator ensures that planned line stops are used effectively, work orders are prepared and scheduled properly, and the right resources are assigned so maintenance work can be executed safely and efficiently with minimal disruption. Responsibilities - Plan and schedule preventive and corrective maintenance activities around planned line stops. - Allocate prepared work orders to the right technicians based on skills, availability, and priority. - Work closely with production planning and maintenance team leads to align priorities and timing. - Prepare and manage maintenance plans and work orders using planning tools and systems (e.g., Excel and a CMMS such as SAP PM). - Re-plan and adjust schedules when urgent deviations or unplanned issues arise, ensuring clear communication to all stakeholders. - Support capacity and resource planning to ensure the right coverage during maintenance windows. - Contribute to improvements in planning processes, ways of working, and reliability performance. - Maintain accurate documentation and ensure work is coordinated with a strong safety and compliance mindset. Requirements - Proven experience in planning and scheduling within an operational or technical environment. - Strong organizational skills and the ability to prioritize in a changing environment. - Excellent communication skills and confidence working with multiple departments. - Strong MS Office skills, especially Excel. - Fluent in both Dutch and English (spoken and written). - Experience with maintenance planning systems (e.g., SAP PM) is a strong advantage. - A proactive, accurate, and collaborative working style. -Temporary Full-Time Contract - (12 Months) Other Information This role requires regular presence on site, with limited flexibility for remote working depending on operational needs. If you are interested and want to apply, please submit your application via the apply button below and contact me.

Company A leading life sciences organisation working in a highly regulated environment. The site supports advanced therapies and operates to strict quality and safety standards. Teams work at pace, with a strong focus on compliance, precision, and delivering results right first time. Job Description The QC Sample Management Technician supports the Quality Control organisation by keeping samples and environmental monitoring (EM) plates moving smoothly into the QC laboratories. The role is hands-on and detail-focused, covering sample receipt, distribution, storage transfers and documentation in line with GxP requirements. This position suits someone who enjoys structured work, takes ownership, and can maintain accuracy in a continuous sample flow. Responsibilities -Receive QC samples and EM plates and ensure they are handled and routed correctly -Distribute samples to QC labs in line with timelines and approved procedures -Perform sample accession activities and complete associated documentation accurately -Transfer samples from -80°C storage to liquid nitrogen storage following safety and handling requirements -Dispose of samples according to procedure and within required timeframes -Maintain a tidy, inspection-ready sample management area (housekeeping) -Maintain 5S standards and support Kanban-managed areas -Follow GxP procedures and complete required training on time -Escalate deviations/non-conformities promptly and support follow-up actions -Contribute to small continuous improvement initiatives to strengthen workflows -Carry out other QC support tasks as needed Requirements -Secondary laboratory education (or similar practical laboratory background) -Experience working in a regulated environment (GMP/GDP/SOP-driven) is preferred -Sample management and/or QC experience within pharma/biotech is an advantage -Strong attention to detail, organisation skills, and a “right-first-time” mindset -Comfortable working in a fast-paced environment with continuous sample flow -Able to communicate clearly and read English in a collaborative workplace -Confident using standard office tools (e.g., Microsoft Office) -Willing and able to work shifts, including evenings, weekends and bank holidays; overtime may be required -Able to be onsite early and work late due to shift times (driving licence preferred) Other Information If you are interested and want to apply, please submit your application via the apply button below and contact me.  

QC Sample Management Technician - Hoofddorp Company Our client is a biotechnology company focused on developing innovative immunotherapies and engineered T-cell treatments for patients with cancer. The organisation operates in a fast-paced, collaborative environment where quality, safety and continuous improvement are essential. Job Description The QC Sample Management Technician will join the Quality Control Services team and support the accurate and compliant handling of laboratory samples. The role involves managing the flow, storage, distribution and disposal of QC samples while following GxP requirements, approved procedures and safety regulations. This position is well suited to a hands-on and organised professional who can work accurately in a high-volume laboratory environment and maintain a strong focus on getting things right the first time. Responsibilities Maintain housekeeping standards in the QC sample management area. Maintain 5S and Kanban areas. Receive QC samples and environmental monitoring plates. Distribute samples to QC laboratories. Transfer samples from ultra-low-temperature storage to liquid nitrogen storage. Perform sample accessioning activities in accordance with procedures. Dispose of samples safely and within the required timelines. Follow approved procedures, SOPs and GxP requirements. Complete required training within the agreed timelines. Escalate deviations and other non-conformities promptly. Support small improvement projects involving procedures and workflows. Assist other QC teams when required. Perform additional duties as assigned. Requirements Secondary laboratory education, such as MLO level 3 or 4, or a similar qualification. Experience in a technical QC role within the biotechnology or pharmaceutical industry is preferred. Experience with laboratory sample management is an advantage. Basic laboratory techniques and strong aseptic working skills. Knowledge of GMP, GDP and SOPs. Good organisational skills and a precise, quality-focused approach. Proficiency with Microsoft Office applications. Ability to communicate verbally and read instructions in English. A hands-on, flexible and collaborative attitude. Willingness to work shifts, weekends, bank holidays and overtime when required. 

Company A leading international consumer goods organisation with a strong portfolio of well-known personal care products. The business operates across multiple European markets and is focused on delivering impactful innovation, smooth product launches, and continuous operational improvement through close cross-functional collaboration. Job Description For a European personal care team, we are looking for a European Innovation Project Coordinator to support innovation leaders and independently drive smaller innovation and renovation projects through to launch. The European Innovation Project Coordinator will coordinate stakeholders across multiple countries, ensure governance requirements are completed, and keep deliverables on track in a fast-paced, complex environment. Responsibilities -Manage and progress innovation/renovation projects from scope definition through launch readiness, ensuring timelines and deliverables are met. -Support Innovation Managers and Strategy Leads with project execution while taking ownership of assigned workstreams. -Coordinate cross-functional collaboration across R&D, Supply Chain, Marketing, and Finance to resolve operational issues and remove blockers. -Align market stakeholders across multiple countries, clarify expectations, and manage competing priorities and requests. -Support budget coordination and tracking for projects where required. -Coordinate adaptation and delivery of communication materials for local market needs and compliance requirements. -Organise and lead project meetings (agenda, stakeholder follow-ups, status reporting, documentation). -Track innovation performance inputs and contribute to reviews and continuous improvement discussions. Requirements -Experience in innovation, deployment, or project coordination roles (consumer products environment preferred). -Strong stakeholder management skills and confidence working with multiple countries/markets. -Proven ability to run cross-functional projects and work independently in complex organisations. -Excellent communication and organisation skills; able to prioritise under pressure. -Proactive, resilient, and comfortable finding compromises when requirements conflict. -Willingness to work on-site in Rotterdam, Netherlands for part of the week (minimum two days). 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 organisation in the regulated life-sciences industry is seeking additional support on site. The company operates in a highly controlled GMP environment where quality, safety, and compliance are essential to daily operations. Job Description The GMP Validation & Calibration Specialist will support validation and calibration activities within a pharmaceutical/GMP setting. The role combines hands-on technical work with accurate documentation, reporting, and strict adherence to SOPs and work instructions. The specialist will work independently on site and contribute to maintaining reliable, compliant operations. Responsibilities - Execute validation and calibration activities in accordance with GMP requirements, SOPs, and work instructions. - Perform hands-on technical support related to equipment and measurement activities (including temperature measurements where applicable). - Prepare, complete, and maintain clear technical documentation and reports with a strong focus on accuracy and traceability. - Support compliant operation of process equipment used within the site’s regulated environment. - Work effectively with Dutch-language and English-language documentation, including contributing to SOPs, work instructions, and reports. - Operate independently on site, ensuring work is delivered to a high standard and within agreed timelines. Requirements - Higher professional education level (HBO or equivalent). - Proven experience in a GMP/pharmaceutical environment. - Hands-on experience with validation, calibration, and technical documentation/reporting. - Fluent Dutch (required due to Dutch-language SOPs, work instructions, and reports). - Good command of English. - Able to work accurately and independently in a regulated environment. - Strong advantage: experience with autoclaves, temperature measurements, and process equipment. - .Solid industry experience is preferred (not a junior profile) 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 Our client is a large, international organization operating in a fast-moving, highly regulated environment with complex manufacturing and supply chain networks across multiple sites. The business is currently going through a significant operational transition, requiring strong coordination across factories and cross-functional teams to protect continuity and readiness. Job Description The Supply Chain Manager will play a central role in keeping a major supply chain transition programme on track. This person will coordinate priorities, dependencies, milestones and decisions across multiple workstreams, ensuring operational readiness and business continuity while the future operating model is being designed and implemented. The role is based on-site in Rotterdam (Netherlands) and involves working closely with factory and operational stakeholders. Occasional travel (around 10%) is expected for workshops and stakeholder sessions in the Netherlands. Responsibilities -Act as a key coordination link between programme workstreams, ensuring alignment on priorities, dependencies, actions and decisions. -Maintain structured tracking of actions and milestones, ensuring critical deliverables remain on schedule. -Monitor progress, highlight bottlenecks early, and escalate risks or delays when required. -Coordinate day-to-day activities across supply chain, manufacturing and related functions to support overall programme execution. -Engage with factories and operational teams to support readiness activities, solve issues, and collect required input. -Manage programme data requests and reporting, ensuring information is accurate, complete and delivered on time. -Identify and manage risks, issues, assumptions and dependencies, proposing practical mitigation actions. -Support discussions around operational setup changes (e.g., services, permits, security, quality readiness) to enable a smooth “Day 1” transition. -Participate in and help organise stakeholder workshops across the Netherlands. Requirements   -Solid experience in manufacturing and/or supply chain within a complex operational environment (FMCG or similar). -Proven ability to coordinate multi-stakeholder projects with multiple workstreams and tight timelines. -Comfortable working in factory/operations settings and engaging with operational teams. -Strong organisation skills: planning, tracking, reporting and follow-through. -Hands-on approach to resolving issues and removing blockers. -Experience with risk/issue management and stakeholder communication at different seniority levels. -Engineering or operations-related education/background is a strong advantage. Other Information If you are interested and want to apply, please submit your application via the apply button below and contact me. This position is on-site in Rotterdam, with approximately 10% travel for workshops/meetings within the Netherlands.

About the Company An international organization operating in the healthcare industry, focused on maintaining high standards of product quality, manufacturing compliance and patient safety. Role Description As a Quality Engineer, you will provide quality systems and compliance support across manufacturing operations and external manufacturing partners. You will oversee quality performance, audits and process improvement activities, while addressing complex product and manufacturing issues and ensuring compliance with applicable quality standards. Key Responsibilities Support the design, implementation and maintenance of quality systems and manufacturing processes. Assess compliance with GMP, ISO standards and Equipment Engineering Systems (EES) requirements. Oversee quality system audits and identify areas requiring corrective action or improvement. Investigate and resolve product and process complaints, defects and quality issues. Monitor contract manufacturer performance through quality metrics and management reviews. Establish and maintain measurement systems to evaluate quality and reliability performance. Identify, contain, correct and prevent product and process defects. Prepare and present quality performance reports and improvement recommendations to management. Provide technical quality support for complex manufacturing processes being transferred to other facilities. Requirements Experience in Quality Engineering or Quality Systems within a GMP manufacturing environment. Strong knowledge of GMP, ISO standards and manufacturing quality systems. Experience with quality audits, compliance assessments and process improvement. Knowledge of complaint handling, defect investigation and corrective and preventive actions (CAPA). Experience monitoring supplier or contract manufacturer quality performance. Ability to analyse quality metrics and translate findings into improvement actions. Strong technical problem-solving and analytical skills. Experience supporting manufacturing processes and/or technology transfers is advantageous.

Company Our client is a large, well-established organisation with a strong focus on safe operations and compliance. The site environment is dynamic and collaboration-driven, with multiple stakeholders working together to maintain high standards in safety, health and environmental performance. Job Description We are looking for a SHE Project Specialist (Process Safety & Hazardous Substances) to take ownership of several SHE-related improvement projects within the department. The role is focused on delivering practical, high-quality outcomes such as gap analyses, training content and procedure updates. This position is fully on site and requires someone who can work independently while partnering closely with internal teams. Responsibilities - Deliver SHE improvement projects within the department from start to finish. - Carry out SWIFTS activities and translate findings into clear follow-up actions. - Prepare and structure TRA training content based on internal procedures and ways of working. - Perform gap analyses linked to relevant guidelines and site requirements, and document results clearly. - Support gap analysis work on hazardous-substance related topics and follow up on action plans. - Review, update and improve procedures related to hazardous substances management in collaboration with another SHE specialist. - Work with stakeholders across the organisation to ensure alignment, progress and adoption of improvements. - Contribute to process safety discussions where relevant, including risk-based thinking and structured reviews. Requirements - Higher professional (HBO) working and thinking level and qualified at HVK level. - Several years of relevant SHE experience, with proven ability to run projects independently. - Hands-on experience with hazardous substances and relevant guidelines/standards (e.g., PGS). - Knowledge of ARIE legislation; experience with HAZOP is preferred. - Strong analytical skills and the ability to work effectively with different stakeholders. - Comfortable working in a large organisation and navigating multiple teams. - Fluent in Dutch and English; able to write procedures in Dutch. -Temporary Contract - 6 Months, Part-Time for 24hrs per week Other Information This role is performed fully on site and the selection process includes two interviews (first on site, second online). If you are interested and want to apply, please submit your application via the apply button below and contact me.