Sales Support Coordinator, Venlo, Limburg

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 A leading manufacturing organization focused on optimizing production processes and ensuring seamless supply chain operations. The company values collaboration, innovation, and continuous improvement in a dynamic environment. Job Description We are seeking a dedicated Production Planning Specialist to join our team in Leeuwarden. In this role, you will develop and manage detailed production schedules across multiple factories to maximize efficiency and meet customer delivery targets. The ideal candidate is experienced, proactive, and enjoys working in a fast-paced manufacturing setting. Responsibilities - Develop, monitor, and adjust production plans for three factories to ensure optimal output. - Collaborate daily with manufacturing teams to review production progress, identify necessary adjustments, and implement improvements. - Coordinate closely with supply planning, warehouse, and transportation teams on material availability, order status, and shipment schedules. - Ensure timely and accurate communication of planning updates to all relevant departments. - Make data-driven decisions, analyze production performance, and identify opportunities for process enhancements. - Manage changing priorities and adapt plans as needed to meet delivery deadlines. - Support ongoing projects aimed at improving planning processes and overall efficiency. Requirements - Minimum HBO level education in (Technical) Business Administration, Supply Chain Management, Logistics, or a related field. - Several years of planning experience within a manufacturing environment. - Strong knowledge of ERP systems, preferably SAP, and familiarity with planning tools such as OMP or similar. - Good analytical skills and capacity to think creatively when addressing planning challenges. - Stress-resistant, team-oriented, and capable of taking responsibility for your planning area. - Excellent communication skills in Dutch; English proficiency is preferred. - Willingness to work outside regular hours when necessary. 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 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.  

About the Company Our client is an international pharmaceutical organization focused on the development and production of high-quality medicines. Within a regulated production environment, the organization places strong emphasis on GMP compliance, quality assurance, continuous improvement and patient safety. Role Description As a QA Production Specialist, you will provide quality assurance support to pharmaceutical production, covering both bulk manufacturing and packaging activities. You will support production teams with deviations and quality issues, lead or contribute to root cause investigations and CAPAs, and assess the impact of deviations on production activities. You will also review GMP documentation, support audits and compliance investigations, contribute to improvement projects and provide quality-related training and knowledge transfer within the organization. Key Responsibilities Provide QA support to pharmaceutical production, including bulk manufacturing and packaging. Support production teams with deviations, quality issues and compliance questions. Assess deviations and advise whether production activities should be halted when required. Investigate and document deviations, complaints, root causes and CAPAs. Monitor production processes and identify deviations from established procedures. Review SOPs, validation protocols, BMRs and other GMP documentation. Participate in change controls, CAPAs, audits and compliance investigations. Develop and implement continuous improvement and quality improvement initiatives. Provide recommendations regarding product safety, occupational health and environmental matters. Deliver training and knowledge transfer and collaborate with Production, QA, QPs, Engineering and other stakeholders. Requirements Master's degree or equivalent academic working level, preferably in Pharmacy, Chemical Engineering or a related field. Experience within the pharmaceutical industry and production environment. Knowledge of (aseptic) pharmaceutical processes and production control systems. Strong knowledge of GMP and Quality Assurance systems. Experience with deviations, root cause investigations and CAPAs. Experience reviewing SOPs, BMRs, validation protocols and GMP documentation. Strong analytical, advisory, communication and reporting skills. Excellent command of spoken and written English. Ability to work effectively in a dynamic and demanding production environment. Strong quality-oriented, collaborative and results-driven mindset.

About the Company Our client is an international food production organization specializing in frozen food products. Within a structured production and packaging environment, the organization focuses on delivering safe, high-quality products while maintaining efficient production processes and strong food safety standards. Role Description As an All-round Packing Operator, you will be responsible for operating, setting up, changing over and monitoring various packaging, box forming and palletizing systems. You will use your technical knowledge to resolve minor technical issues, monitor product quality and ensure a smooth production flow. Working closely with packing staff, assistant operators and supervisors, you will contribute to safe, efficient and high-quality production in a 3-shift environment. Key Responsibilities Set up, operate, change over and monitor packaging, box forming and palletizing systems. Perform quality and safety checks and accurately record results. Monitor product flow and make adjustments when deviations or malfunctions occur. Resolve minor technical breakdowns and involve the Technical Service when required. Coordinate daily activities with packing staff and assistant operators on assigned lines. Ensure correct processing, packaging and palletizing according to the production schedule. Follow applicable food safety, quality and hygiene procedures. Contribute to an orderly, clean and safe working environment. Participate actively in shift handovers and communicate relevant information clearly. Support smooth production and contribute to achieving planned production orders. Requirements At least 2 years of relevant experience in a production or packaging environment. Knowledge of HACCP and Food Defense. Experience or ability to provide and follow safety instructions. Experience with or willingness to participate in on-the-job training. Knowledge of allergens and food safety requirements. Technical understanding and a hands-on approach to resolving minor breakdowns. Able to work effectively with colleagues in a production and shift environment. Structured and quality-focused approach to working. Willingness to work in a 3-shift system: 07:15–15:15, 15:15–23:15 and 23:15–07:15.

Over het bedrijf Onze opdrachtgever is een internationale farmaceutische organisatie die actief is binnen een sterk gereguleerde omgeving, met een sterke focus op productkwaliteit, compliance en continue verbetering binnen productie- en kwaliteitsprocessen. Functieomschrijving Als QA Officer ondersteun je diverse Quality Assurance-activiteiten binnen een GMP-gereguleerde farmaceutische of biotechomgeving. Je draagt bij aan het behandelen van afwijkingen en CAPA's, root cause investigations, validatie- en kwalificatieactiviteiten en het beoordelen van kwaliteitsdocumentatie. Je werkt nauwkeurig volgens vastgestelde kwaliteitssystemen en schakelt effectief met verschillende interne en cross-functionele stakeholders. Belangrijkste verantwoordelijkheden Ondersteunen bij het behandelen en onderzoeken van GMP-afwijkingen. Bijdragen aan het opstellen, implementeren en opvolgen van CAPA's. Ondersteunen van root cause investigations met passende onderzoeksmethodieken. Deelnemen aan validatie- en kwalificatieactiviteiten. Beoordelen van GMP-documentatie op juistheid en compliance. Ondersteunen van Quality Assurance-activiteiten binnen farmaceutische of biotechproductie. Samenwerken met verschillende afdelingen rondom kwaliteits- en compliancevraagstukken. Zorgdragen voor een correcte en volledige documentatie van kwaliteitsactiviteiten. Functie-eisen Een relevante bacheloropleiding of gelijkwaardig niveau binnen een wetenschappelijke, farmaceutische of technische richting. Aantoonbare ervaring binnen een GMP-gereguleerde Sterke ervaring met deviations, CAPA's en root cause investigations. Ervaring met validatie en kwalificatie. Ervaring met het beoordelen van GMP-documentatie. Goede kennis van GMP-principes en kwaliteitssystemen. Vloeiende beheersing van Nederlands en Engels, zowel mondeling als schriftelijk.

Over het bedrijf Onze opdrachtgever is een internationale producent binnen de voedingsmiddelenindustrie waar kwaliteit, voedselveiligheid en continu verbeteren centraal staan. Je komt terecht in een dynamische productieomgeving waar samenwerking, ontwikkeling en eigenaarschap worden gestimuleerd. Functieomschrijving Als Voorman combineer je operationele werkzaamheden met het coördineren van de dagelijkse productie. Je bent het eerste aanspreekpunt voor medewerkers en teamleiders, bewaakt de voortgang van het productieproces en zorgt ervoor dat kwaliteit, voedselveiligheid en veiligheid altijd worden nageleefd. Daarnaast begeleid en coach je collega's en draag je actief bij aan een efficiënte en veilige werkomgeving. Belangrijkste verantwoordelijkheden Coördineren en ondersteunen van de dagelijkse productieactiviteiten. Operationeel aansturen, begeleiden en coachen van productiemedewerkers. Actief meewerken binnen productie, inpak of bereiding. Toezien op naleving van HACCP-, Food Defence-, allergenen-, kwaliteits- en veiligheidsvoorschriften. Geven van veiligheidsinstructies aan medewerkers. Bewaken van standaarden zoals 5S en SMED. Zelfstandig oplossen van kleine storingen en afstemmen met de Technische Dienst bij complexe storingen. Opstellen en beheren van werkinstructies en procedures. Begeleiden en inwerken van nieuwe medewerkers. Intensief samenwerken met Productie, Logistiek, QESH en de Technische Dienst. Functie-eisen MBO werk- en denkniveau met minimaal 2 jaar relevante ervaring. Ervaring binnen de voedingsmiddelenindustrie. Kennis van HACCP, Food Defence en allergenenbeheer. Ervaring met het geven van veiligheidsinstructies en het coachen van medewerkers. Praktische en hands-on instelling met een proactieve houding. Ervaring met het coördineren van productieprocessen. Goede communicatieve en leidinggevende vaardigheden. Goede beheersing van de Nederlandse taal.