Data Transformation Specialist, Utrecht, Utrecht

Company Overview A leading organization dedicated to innovation and excellence in the personal care industry. The company fosters a collaborative environment focused on delivering quality products and strategic growth across Europe. Job Description We are seeking an experienced Supply Chain Finance Manager to join our client’s team. This role is central to managing financial performance and providing strategic insights within the Personal Care Supply Chain across Europe. The successful candidate will be responsible for overseeing planning, forecasting, cost control, and performance management, supporting the business in achieving its financial objectives in a dynamic and innovative environment. Responsibilities -Lead performance management initiatives, including monitoring cash flow, working capital, and key financial metrics. -Conduct regular reviews of performance against plans, providing clear commentary on variances and risks. -Drive planning and forecasting for supply chain overheads and operational costs. -Collaborate with senior management to interpret financial data, highlighting trends and efficiencies to guide decision-making. -Perform scenario analysis and financial modeling to evaluate cost implications and operational strategies. -Translate complex data into clear narratives, supporting a data-driven decision culture. -Ensure compliance with internal financial policies, controls, and governance standards. -Continuously improving finance processes, reporting accuracy, and team capabilities. -Mentor and develop junior team members within the finance function, exemplifying strong leadership behaviors. Requirements -Proven experience in financial planning, forecasting, and performance management within a supply chain or FMCG environment. -Strong background in budgeting, cost analysis, and managing key financial KPIs such as working capital and gross margin. -Excellent stakeholder management and communication skills, with the ability to simplify complex financial concepts. -Leadership experience, managing at least two direct reports. -Available for full-time work (40 hours per week) and able to start immediately or by July at the latest. Other Information If you are interested and want to apply, please submit your application via the apply button below and contact me.  

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.  me.

Company Our client is a global, innovation-driven organisation in the life sciences sector. They operate in a highly regulated environment and support international clinical programs by ensuring products are prepared, labelled, and packaged accurately and safely for use worldwide. Quality, compliance, and teamwork are central to how the teams work every day. Job Description For our client in Breda, we are looking for a Packaging Operator (GMP) to support clinical labelling and packaging activities. In this role, the Clinical Packaging Operator (GMP) works in a day-shift team and carries out manual labelling, packaging, and assembly activities according to standard operating procedures. The work requires strong attention to detail, clear communication, and a quality-first mindset. Responsibilities - Execute clinical labelling and packaging activities according to standard operating procedures (SOPs) - Perform manual packaging, labelling, and assembly activities accurately and efficiently - Take ownership of tasks and results within the assigned area of responsibility - Escalate deviations, issues, or unexpected situations when necessary - Complete all required training according to the training plan and deadlines - Support batch-related logistics processes linked to packaging activities - Contribute to improvements in working processes, quality, and efficiency - Work in both room temperature areas and, when needed, in cold-room conditions (2–8°C) Requirements - Experience in a manual packaging environment (preferably within a regulated setting such as GMP/GDP) - Comfortable working according to procedures in a strongly regulated environment - Strong attention to detail; accurate and quality-focused way of working - Team player with clear communication skills and a flexible attitude - Willing and able to work on-site in Breda and adapt to changing priorities - Experience with SAP and/or MES is a plus Other Information The Clinical Packaging Operator (GMP) will join a dedicated team supporting important clinical activities in an international environment. If you are interested and want to apply, please submit your application via the apply button below and contact me.

Company Our client  is known around the world for their chocolate bars, which are some of the most popular. Besides that, they are suppliers of multiple popular pet food brands, as well as several other trademarks. The factory in the Netherlands  currently has the biggest production volume of all the factories, besides being one of the biggest chocolate factories in the world.   Job Description The Strategic Revenue Management Analyst role focuses on improving promotional effectiveness and mix management through deep data analysis. You will translate complex datasets into actionable insights that drive commercial decision-making, enhance profitability, and optimize investment strategies. This role offers strong exposure to cross-functional teams including sales, finance, and category management, making it ideal for professionals looking to grow within FMCG commercial strategy. Responsibilities - Analyze promotional performance across customers, channels, brands, and packs - Evaluate promotion mechanics such as ROI, depth, frequency, and incremental volume - Identify opportunities to improve promotional efficiency and reduce trade spend losses - Support the development of promotion guidelines and decision frameworks - Analyze product mix performance across brands, channels, and customer segments - Build dashboards and reports for commercial teams - Translate complex datasets into clear business insights and recommendations - Support business reviews, planning cycles, and internal strategy discussions - Collaborate with sales, finance, and category management teams Requirements - Minimum 3 years of experience in FMCG, consulting, finance, sales, or commercial analytics - Strong analytical skills with experience working with large datasets - Solid commercial understanding and interest in revenue growth strategy - Ability to turn data into actionable business recommendations - Strong Excel and PowerPoint skills, Power BI and other tools are a plus  - Strong communication skills and ability to present insights clearly - Detail oriented and structured approach to problem solving - Proactive mindset with a willingness to learn Other Information Apply to our vacancy for more information. Looking forward to getting in touch!  

The Company  The client is a global food company famous for confectionery but also pet food.  Role Description The Ocean Visibility Platform Lead is responsible for driving the performance, adoption, and continuous improvement of a global SaaS-based visibility solution that connects over 80 markets, 35 manufacturing sites, and more than 300 users worldwide. Reporting to the Global Ocean Control Tower Lead, this role plays a critical part in transitioning the platform from its post-go-live hypercare phase into a stable Business-as-Usual (BAU) operating model while maximizing business value. This is a predominantly hands-on operational role, focused on the day-to-day management of the platform, including data quality oversight, operational governance, and vendor management (Cargoo). In parallel, the role requires active engagement with global stakeholders, supporting user adoption and ensuring effective communication across logistics teams and leadership forums. Responsibilities Acting as the business product owner, accountable for platform performance, data integrity, and user support. Leading the transition from hypercare to a sustainable BAU operating model. Overseeing end-to-end data quality, ensuring accurate data flows from ERP systems and external partners. Establishing and enforcing data standards, resolving data issues, and drive corrective actions with stakeholders. Designing and implementing governance frameworks, including operating cadence, RACI structures, and escalation protocols. Managing the day-to-day relationship with the SaaS provider, acting as the primary business contact. Defining and monitoring SLAs and KPIs to ensure service performance and data accuracy. Leading periodic and quarterly business reviews (QBRs) to assess performance and align on future priorities. Collaborating on system enhancements and ensuring successful rollout and adoption of new features. Defining and monitoring key value metrics such as visibility coverage, data quality, user adoption, and operational impact. Delivering presentations and leading global townhalls for stakeholders, including Logistics Managers and Supply Chain leaders. Representing the platform in leadership forums as needed. Executing a global user adoption strategy across a diverse and geographically distributed user base. Establishing a network of super-users and regional champions to embed the platform into daily operations. Developing and delivering targeted training programs tailored to different markets and user groups. Requirements Bachelor’s degree in Supply Chain, Logistics, Business, or a related field. Proven experience in supply chain, logistics, or transportation roles; experience with TMS or SaaS logistics platforms is advantageous. Hands-on experience managing or operating a SaaS platform, including data quality management, user support, and vendor coordination. Strong understanding of governance frameworks, KPIs, and operating models. Excellent communication and presentation skills, with the ability to engage global audiences and senior stakeholders. Demonstrated experience in change management and driving user adoption across large, international organizations. Strong analytical and problem-solving capabilities, with a structured and independent working style. Other information   Apply to our vacancy for more information. Looking forward to getting in touch!   

Company A leading biotechnology company dedicated to serving patients worldwide. The organization operates a global supply chain network, manufacturing and distributing medicines and clinical research products. With a diverse team of professionals from multiple countries, it focuses on innovative healthcare solutions and improving patient outcomes.   Job Description We are seeking a detail-oriented and experienced Clinical Supply Chain Associate to join the team. In this role, you will oversee the efficient and compliant distribution of investigational products to clinical sites around the world, ensuring timely delivery and adherence to regulatory standards.   Responsibilities - Manage sales orders and stock transfer order processes - Review and monitor temperature data and handle temperature excursions - Control site and transit temperature deviations, including returns and reconciliation - Support expiry relabeling activities and oversee import license processes - Handle and resolve distribution complaints efficiently - Ensure compliant and timely delivery of investigational products to clinical sites - Collaborate with customer service, supply chain teams, QA, warehouses, and logistics partners - Maintain accurate documentation and track key performance indicators Requirements - Bachelor degree in Supply Chain Management or a related field - At least 2 years of experience in supply chain, preferably in a regulated environment - Strong knowledge of regulatory requirements for clinical supplies - Proficiency in English, both written and spoken - Experience with ERP systems - Skilled in Microsoft Office and automated business systems Other Information - Global role with collaboration across multiple teams and regions - Strong focus on compliance, documentation, and quality standards - Opportunity to work in a regulated and innovative healthcare environment  If you are interested and want to apply, please submit your application via the apply button.

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

The Company A leading pharmaceutical manufacturing organization specializing in high quality medical products within a highly regulated GMP environment. The company operates advanced automated production lines and focuses on continuous improvement, operational excellence, and delivering safe and effective medicines to patients. Role Description The Manufacturing Process Technician is responsible for operating and optimizing production lines in a controlled and regulated environment. The role focuses on maintaining high quality standards while ensuring process efficiency and continuous improvement. You will work closely with operators, line leads, and supervisors to ensure smooth operations and consistent output. Responsibilities Operate and monitor production lines according to standard operating procedures Perform changeovers and ensure manufacturing processes run efficiently Collect, document, and analyze production data Handle administrative tasks within SAP and MES systems Identify process deviations and initiate escalation when required Contribute to continuous improvement initiatives using Lean methodologies Collaborate with team members to meet production targets Troubleshoot technical issues and support root cause analysis Ensure proper shift handover with accurate documentation Follow all training requirements and compliance standards Support logistics and material flow processes Requirements - Minimum 5 years of experience in a manufacturing or process operator role - Experience in GMP, GDP, or ISO regulated environments - Knowledge of Lean manufacturing, Six Sigma, and continuous improvement methods - Experience with ERP systems such as SAP or MES - Familiarity with standard operating procedures - Technical or process related education such as MBO, VAPRO A, or VAPRO B - Strong communication skills in English and Dutch - Proficiency in Microsoft Office tools - Analytical mindset with strong problem solving skills - Ability to work flexible shifts including weekends and overtime Other Information - Shift based role in a manufacturing environment - Work involves collaboration within teams of 3 to 9 operators per line - Focus on safety, quality, and compliance - Opportunities for process improvement and professional development

The company:  A global biotechnology leader focused on developing innovative therapies specializes in advancing biologic medicines across areas such as oncology, cardiovascular health, inflammation, bone health, and rare diseases, with a strong emphasis on scientific research, innovation, and improving patient outcomes. Role description : we are looking for a Senior Associate Quality Assurance (GMP) to support product quality complaint handling and related investigations in a regulated pharmaceutical environment. Key responsibilities -Initiate and own product quality complaints, safety quality investigations, and product security investigations  -Partner with global/other-site QA teams and external partners to resolve investigations -Collaborate with in-country affiliates and intake call centers on intake procedures and complaint follow-up -Prepare, review, and approve procedures/work instructions in line with GMP, site, and regulatory requirements -Support site projects and continuous improvement initiatives -Provide training to internal and affiliate staff on complaint handling and investigation execution -Initiate and own QA Non-Conformances / CAPAs where required -Participate in audits and inspections (internal, third party, and regulatory) related to the complaint handling process Requirements : -MBO or Bachelor’s degree (or equivalent) with ~3+ years relevant experience or Master’s degree (or equivalent) with minimal related experience -Fluent English -Experience working in a regulated/GxP environment with a strong compliance mindset -Strong analytical skills and the ability to identify, reconcile, and resolve data integrity issues Other Information -If you are interested and want to apply, please submit your application via the apply button below and contact me.  

Company Overview An innovative leader in consumer electronics, specializing in the development of high-quality grooming and beauty appliances. The company is committed to delivering cutting-edge products that enhance personal care routines with functionality, durability, and sleek design. Job Description We are seeking a skilled Mechanical Design Engineer to join a dynamic product development team focused on grooming and beauty appliances. In this role, you will oversee the mechanical design and development of products such as shavers, groomers, epilators, and IPL devices, from initial concept through to mass production. Your expertise will help bring innovative, high-performance appliances to market that deliver real value to customers worldwide. Responsibilities -Design and detail mechanical components and systems according to product specifications. -Conduct predictive analyses and calculations to ensure functionality and manufacturability. -Select appropriate materials (metals and plastics) and manufacturing processes. -Create detailed 3D and 2D drawings, ensuring they meet manufacturing and assembly requirements. -Manage product specifications, lead DFMEA processes, and adhere to the V-model development methodology. -Develop prototypes, lead ideation sessions, and drive concept validation and decision-making. -Plan and prioritize workload, collaborating seamlessly with multidisciplinary teams using agile methods. -Write test protocols, conduct tests, analyze results, and develop new testing methods where needed. -Work closely with colleagues in systems engineering, electronics, manufacturing, and procurement to ensure project success. -Document design decisions, maintain records in a design history file, and archive files in Windchill. -Drive continuous improvement initiative identifying gaps and implementing enhancements within the mechanical engineering group. Requirements -Bachelor’s degree in mechanical engineering or related field. -3-5 years of experience in mechanical product design for mass production. -Proficiency in 3D CAD software (Siemens NX or CREO). -Strong knowledge of designing plastic and metal components with manufacturability and tooling in -mind. -Experience with CFD, FEA (e.g., Ansys), and other analytical software is a plus. -Familiarity with geometric dimensioning and tolerancing. -Proven ability to develop prototypes quickly and move concepts into production. -Good communication skills and the ability to work effectively in a team environment. -Experience with Design for Six Sigma (greenbelt certification is advantageous). -Knowledge of medical devices or experience in the medical device industry is a plus but not required. Other Information If you are interested and want to apply, please submit your application via the apply button below