Supply Chain Account Manager, Amersfoort, Utrecht

Company: Our client is a leading organization dedicated to operational and business excellence across highly regulated industries. They are committed to continuous improvement, innovation, and delivering the highest standards in their processes. Job Description: We are seeking an experienced Business Excellence Specialist to support and drive Lean Six Sigma initiatives within their operations. This role involves coaching teams, implementing process improvements, and contributing to the organization’s manufacturing and operational excellence strategies. Responsibilities: - Assist in executing projects and initiatives aimed at improving manufacturing and business processes. - Support the development and documentation of new and existing manufacturing procedures to maximize efficiency and cost-effectiveness. - Conduct simple trend analyses and contribute to continuous improvement efforts. - Collaborate with stakeholders to develop and establish key performance indicators (KPIs) and performance tracking systems. - Provide basic training on Lean principles and tools to team members. - Identify opportunities for process enhancements through observation and data analysis. - Support the implementation of lean tools such as standardized work, work charts, and training matrices. - Drive focused continuous improvement activities aligned with KPIs. - Foster cross-site collaboration to share best practices and ensure consistency. - Promote understanding of Johnson & Johnson’s Credo and Leadership Imperatives in daily activities. Requirements: - At least 3 years of experience in Business or Operational Excellence. - Lean Black Belt certification or equivalent hands-on experience in leading continuous improvement initiatives. - Strong knowledge of Lean Six Sigma tools and methodologies. - Relevant degree (HBO level or similar), with a focus on business or technical disciplines. - Proficiency in English (B2 level). - Intermediate MS Office skills; data analysis and business applications knowledge preferred. - Positive, proactive, and organized attitude. - Ability to work independently and as part of a team. - High attention to detail and a drive for quality. - Strong analytical thinking and problem-solving skills. - Ability to handle changing priorities and work under pressure. - Excellent stakeholder management and communication skills. 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 organization in the consumer goods industry, dedicated to delivering innovative and high-quality products in personal care and beauty wellbeing. They focus on building strong relationships with retail partners and consumers alike, driving growth through strategic account management and market insights. Role Description   As a Key Account Manager, you are responsible for managing the Personal Care and Beauty Wellbeing portfolio for a major retail customer. You will drive sales objectives, product launches, promotional planning, and commercial performance, while building strong relationships with customers and collaborating closely with Customer Development, Marketing, Finance, Supply Chain, and Operations teams. Responsibilities - Manage and develop the Personal Care and Beauty Wellbeing portfolio for the assigned retail customer. - Support customer management, product launches, and promotional planning. - Work with the CSP team to deliver effective commercial offerings and financial outcomes. - Analyze sales performance and market insights to support business decisions. - Collaborate with Customer Development, Marketing, Finance, Supply Chain, and Integrated Operations. - Build and maintain strong relationships with key customers and internal stakeholders. - Contribute to achieving joint sales targets and commercial objectives. - Support the development of effective customer and sales strategies. Requirements - Experience in Key Account Management, Customer Development, Sales, or a related commercial role. - Experience within FMCG, Consumer Goods, Personal Care, Beauty, or Retail is preferred. - Strong commercial mindset with a focus on achieving business and sales objectives. - Excellent relationship-building and negotiation skills. - Strong ability to create win-win outcomes and build long-term partnerships. - Highly social, collaborative, and stakeholder-focused. - Strong communication, organizational, and analytical skills. - Ability to work effectively across multiple cross-functional teams. Other Information If you are interested and want to apply, please submit your application via the apply button below and contact me.

Het Bedrijf Onze opdrachtgever is een toonaangevende zuivelcoöperatie met een wereldwijde aanwezigheid en een rijke geschiedenis van meer dan 150 jaar. De organisatie richt zich op de productie van hoogwaardige voedingsingrediënten en zuiveloplossingen en is sterk gericht op innovatie, duurzaamheid en operationele excellentie binnen een geautomatiseerde en hygiënische productieomgeving. Functieomschrijving Als MRP Planner ben je verantwoordelijk voor de operationele planning van ingrediënten, verpakkingsmaterialen en grondstoffen en zorg je ervoor dat de productie tijdig wordt beleverd. Je werkt nauw samen met leveranciers en interne stakeholders en ondersteunt daarnaast verschillende verbeter-, IT- en productieprojecten. Je bent proactief en hands-on, signaleert knelpunten en optimaliseert voorraad- en planningsprocessen binnen een dynamische productieomgeving. Verantwoordelijkheden Verantwoordelijk voor de operationele MRP-planning van ingrediënten, verpakkingsmaterialen en grondstoffen. Optimaliseren van de planning op basis van vraag, voorraad, leverancierscondities en productiebehoeften. Signaleren en oplossen van knelpunten en afwijkingen binnen de supply chain. Nauw samenwerken met leveranciers, productie, logistiek en andere interne stakeholders. Bijdragen aan IT-, productie-, leveranciers- en verbeterprojecten. Continu verbeteren van planningsprocessen, procedures en efficiëntie. Functie-eisen Minimaal 3 jaar ervaring als MRP Planner, Materiaalplanner, Supply Planner of vergelijkbare functie. HBO/WO werk- en denkniveau, bij voorkeur binnen Supply Chain, Logistiek of Planning. Ervaring met MRP en planningstools, bij voorkeur SAP ECC, SAP APO of OMP. Ervaring binnen een productieomgeving; FMCG, food of dairy is een sterke pré. Sterke analytische, organisatorische en probleemoplossende vaardigheden, met oog voor detail. Nederlands is vereist en goede beheersing van Engels is een pré. Overige informatie Solliciteer op onze vacature voor meer informatie. We kijken ernaar uit om van je te horen!

Company  Our client is a leading organisation within the pharmaceutical manufacturing sector, operating a highly regulated production site in the Netherlands. The company is known for strong quality standards, structured ways of working, and a strong focus on safety, compliance, and continuous learning on the shopfloor. Job Description  For a regulated production site in Haarlem, we are looking for a Production Operator (GMP Environment). In this role, the operator supports daily production by executing assigned tasks safely, accurately, and fully in line with approved procedures. The position suits someone who enjoys structured work, takes ownership of doing things right the first time, and escalates issues quickly when something deviates from the standard. Responsibilities  The Production Operator (GMP Environment) will: - Execute assigned production activities according to approved procedures, safety requirements, and quality standards - Prepare tasks, materials, and work areas as instructed - Operate equipment as trained and follow agreed working methods - Apply GMP principles and ensure correct, timely documentation of all own activities - Recognise deviations, abnormalities, or safety concerns and escalate them in line with established escalation rules - Work closely with colleagues within the production team and follow structured handover and communication practices - Participate in training and on-the-job learning to build technical knowledge and practical skills Requirements – keep to key points only - MBO level education, preferably in a technical, production, or life-science related field - Fluent in both Dutch and English (spoken and written) - Comfortable working in a structured, regulated production environment - Accurate, detail-oriented working style and strong discipline in following procedures - Team-oriented attitude with clear communication during handovers and daily collaboration - Temporary Full-Time Contract (1 Year) - Willing/able to work 16/5 or 24/5 shifts (incl. nights) Other Information This role is based on-site in Haarlem and involves working in a structured shift environment. A pre-employment screening may be part of the process. 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 organisation within the pharmaceutical manufacturing sector, operating a highly regulated production site in the Netherlands. The company is known for strong quality standards, structured ways of working, and a strong focus on safety, compliance, and continuous learning on the shopfloor. Job Description  For a regulated production site in Haarlem, we are looking for a Production Operator (GMP Environment). In this role, the operator supports daily production by executing assigned tasks safely, accurately, and fully in line with approved procedures. The position suits someone who enjoys structured work, takes ownership of doing things right the first time, and escalates issues quickly when something deviates from the standard. Responsibilities  The Production Operator (GMP Environment) will: - Execute assigned production activities according to approved procedures, safety requirements, and quality standards - Prepare tasks, materials, and work areas as instructed - Operate equipment as trained and follow agreed working methods - Apply GMP principles and ensure correct, timely documentation of all own activities - Recognise deviations, abnormalities, or safety concerns and escalate them in line with established escalation rules - Work closely with colleagues within the production team and follow structured handover and communication practices - Participate in training and on-the-job learning to build technical knowledge and practical skills Requirements – keep to key points only - MBO level education, preferably in a technical, production, or life-science related field - Fluent in both Dutch and English (spoken and written) - Comfortable working in a structured, regulated production environment - Accurate, detail-oriented working style and strong discipline in following procedures - Team-oriented attitude with clear communication during handovers and daily collaboration - Temporary Full-Time Contract (1 Year) - Willing/able to work 16/5 or 24/5 shifts (incl. nights) Other Information This role is based on-site in Haarlem and involves working in a structured shift environment. A pre-employment screening may be part of the process. 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 dairy organization focused on producing high-quality dairy products and nutrition solutions. The company operates in a highly professional manufacturing environment with strong emphasis on quality, safety, innovation, sustainability, and continuous improvement. It offers a dynamic workplace where professionals can contribute to efficient production, supply chain performance, and operational excellence. Role Description As a Production Planner, you will play a key role in ensuring smooth and efficient production operations. You will be responsible for creating and optimizing production plans across multiple manufacturing facilities, ensuring material availability, production efficiency, and timely delivery to customers. The role involves close collaboration with Production, Supply Planning, Warehouse, Logistics, and Transport teams. Responsibilities - Create, maintain, and optimize production plans across multiple manufacturing facilities. - Monitor production progress and make planning adjustments when required. - Coordinate material flows, inventory, production orders, and shipments. - Work closely with Production Managers, Supply Planners, Warehouse, and Transport Planners. -  Manage planning data using OMP and SAP/ERP systems. - Monitor stock levels, material availability, and supplier deliveries. - Communicate planning changes clearly to relevant stakeholders. - Identify bottlenecks and develop practical, creative solutions. - Support continuous improvement initiatives within the planning process. Requirements - Experience in Production Planning, preferably within a manufacturing environment. - Strong understanding of planning processes and production flows. - Experience with ERP systems, preferably SAP; OMP experience is a strong advantage. - Strong analytical, problem-solving, and organizational skills. - Proactive, hands-on, and able to take ownership and responsibility. - Strong communication and stakeholder management skills. - Flexible and able to work effectively in a fast-paced environment. - Fluent Dutch is required; English is preferred. - Willingness to participate in on-call services outside regular working hours. - Relevant HBO education is preferred, but relevant experience is more important. 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 organization in the pharmaceutical manufacturing sector dedicated to ensuring the highest standards of quality and safety in production. The company focuses on delivering innovative solutions within a regulated environment, adhering to strict GMP guidelines and continuous improvement initiatives. Job Description: The Quality Assurance Production Specialist is responsible for overseeing and supporting pharmaceutical production processes to ensure compliance with quality standards. This role involves evaluating production activities, supporting quality improvement projects, and maintaining strict adherence to GMP regulations. Responsibilities: -Ensure quality assurance within pharmaceutical production, including bulk manufacturing and packaging operations. -Support production teams in managing deviations and quality issues, including deciding whether to halt production if necessary. -Propose and implement improvements to manufacturing processes and technology. -Provide technical and content support regarding quality matters, including monitoring, investigating, and documenting deviations and complaints. -Conduct root cause analyses and develop corrective and preventive actions (CAPAs). -Lead initiatives for process improvements stemming from audits, deviations, or continuous improvement programs. -Advise on occupational health and safety, product safety, and environmental policies. -Participate in audits, investigations, and compliance responses. -Maintain up-to-date documentation, including SOP reviews, validation protocols, and batch records. -Contribute to project work, change controls, and staff training efforts. -Engage in business unit meetings and collaborations with internal and external stakeholders. Requirements: -Master’s degree or equivalent in Pharmacy, Chemical Engineering, or a related field. -Knowledge of aseptic pharmaceutical processes and production control systems. -Experience working within pharmaceutical manufacturing environments. -Strong communication, analytical, planning, and reporting skills. -Proficiency in English, both spoken and written. -Ability to thrive in a dynamic, regulated setting with attention to detail and quality. -Skills in training, knowledge transfer, and teamwork. 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 producer in the food and beverage industry, committed to sustainability, innovation, and quality. They operate in a dynamic environment where agility and continuous improvement are key to meeting growing market demands. Job Description: We are seeking an experienced MRP Planner to join a fast-paced manufacturing site. In this role, you will be responsible for operational planning related to ingredients, packaging, and chemicals, ensuring smooth production processes. You will support ongoing projects and help manage the transition during a period of significant change within the organization. Responsibilities: •    Manage short- and medium-term operational planning for ingredients, packaging, and chemicals using MRP systems. •    Continuously optimise production schedules by balancing demand, stock levels, supplier conditions, and operational developments. •    Identify opportunities for improvement and resolve any bottlenecks that could impact production. •    Collaborate closely with internal departments and suppliers to ensure production goals are met efficiently. •    Support and participate in various projects, including new product launches, process improvements, and IT upgrades. •    Contribute to ongoing process improvements and develop better working procedures. •    Act as a key contact point for suppliers and internal stakeholders, ensuring clear communication and alignment. Requirements: •    At least 3 years of experience in planning, preferably in a supply chain or logistics role within the FMCG or food industry. •    Strong knowledge of production and logistics operations. •    Experience with planning systems such as SAP ECC, SAP APO, or OMP is highly desirable. •    Excellent organisational skills with attention to detail and a proactive approach. •    Ability to work effectively in a fast-changing environment. •    Good stakeholder management skills, especially in collaboration with external suppliers. •    Fluent in Dutch, with good command of English. Other Information: This is a 6-month temporary position starting as soon as possible, supporting key ongoing projects such as IT implementations, production line upgrades, and supplier changes. The role involves working on-site most of the time, with a maximum of two days working from home. The ideal candidate will be a motivated problem-solver with a hands-on attitude, who can work independently and as part of a team. 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 large industrial production environment where safety, compliance, and operational continuity are critical. The site delivers complex technical projects in a highly regulated setting and works closely with multidisciplinary teams and engineering contractors to ensure reliable, future-proof installations. Job Description We are looking for an Instrumentation & Electrical Engineer (Projects) to support and deliver electrical and instrumentation engineering activities across capital projects, maintenance improvements, and operational support. The Instrumentation & Electrical Engineer (Projects) will provide compliant designs, translate requirements into clear specifications, and help ensure projects are executed safely, efficiently, and to a high technical standard. Responsibilities - Deliver concept designs and translate them into clear, well-documented engineering solutions. - Prepare and review specifications and technical requirements, including quality and process safety considerations. - Coordinate and review engineering deliverables from external contractors to ensure completeness and compliance. - Ensure designs meet applicable standards and internal procedures for electrical and instrumentation work. - Manage and track engineering activities to support delivery against project schedules and budgets. - Act as a technical point of contact for internal stakeholders such as Maintenance, Operations, and Manufacturing/Process Technology. - Support site activities such as commissioning, start-up, troubleshooting, and technical handover where required. - Contribute to continuous improvement initiatives to strengthen project execution and engineering quality. Requirements - Bachelor’s or Master’s degree in Electrical Engineering, Industrial Automation, or a comparable discipline. - Practical engineering experience in an industrial environment (process industry preferred). - Strong working knowledge of relevant electrical/instrumentation standards and directives (e.g., ATEX/IEC 60079, EMC, Machinery Directive, IEC 60204, and common NEN standards). - Solid instrumentation knowledge; affinity with electrical engineering and design is required. - Understanding of process automation and safety-related systems (SIL/SIS knowledge is a plus). - Strong analytical skills, structured problem-solving approach, and clear communication. - Able to manage multiple priorities in a busy, project-driven environment. - Fluent in Dutch and English. - Willingness to complete an online assessment and screening as part of the process. - Temporary Full Time Contract (1 Year Duration) Other Information An online assessment and screening may be part of the recruitment process. 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 global leader in the life sciences industry, committed to improving health and well-being through innovative products and advanced scientific solutions. The organisation operates in a highly regulated environment, with a strong focus on quality, safety, compliance, and continuous improvement. Role Description We are looking for an experienced QC Laboratory Technician – Microbiology to join a dynamic QC team. You will perform and document chemical, biological, and microbiological testing in accordance with GMP standards, ensuring accurate results and high laboratory quality while contributing to continuous improvement and process optimisation. Responsibilities - Perform, document, and review QC tests according to established procedures and standards. - Identify and report OOS results, deviations, and trends in line with GMP procedures. - Perform microbiological testing, including sterility testing, bioburden, environmental monitoring, and aseptic techniques. - Enter test results and perform data analysis and trending. - Participate in and potentially lead continuous improvement projects using Lean/Six Sigma tools. - Review, update, and prepare Work Instructions (WIs) and SOPs. - Ensure compliance with GMP, safety, and quality requirements. - Support a culture of continuous improvement, problem-solving, and operational excellence. Requirements - Completed MBO/MLO Level 4 qualification in Microbiology or a related laboratory discipline. - Previous experience working in a quality-controlled laboratory environment, preferably within GMP. - Practical experience with microbiological testing techniques. - Strong analytical, problem-solving, and organisational skills. - Accurate, quality-focused, and proactive approach to work. - Good communication and teamwork skills. - Good written and verbal communication skills in Dutch and English. - Experience or affinity with Lean/Six Sigma and continuous improvement.    Other Information If you are interested and want to apply, please submit your application via the apply button below and contact me.