The Company Our Company is a European food manufacturer specializing in frozen snacks and appetizers. The company operates multiple production locations across Europe. Role Overview We are looking for a Technical Administrative / Work Order Coordinator to support the Project Department (TD). The main focus of this role is processing data in a new work-order system and maintaining the related dashboard. Key Responsibilities Enter and process data accurately in the new work-order management system. Maintain and update the associated dashboard. Ensure work-order information is accurate and up to date. Support the Technical/Project Department with administrative and data-related tasks. Manage and organize information using Microsoft Excel. Work accurately with technical and administrative information. Requirements HBO-level education is preferred; candidates currently taking a gap year are particularly suitable. MBO-level candidates can also be considered with a strong affinity for technology. Excellent Excel skills are essential. Interest in or affinity with a technical environment. Strong attention to detail, accuracy, and organizational skills. Comfortable working with computer systems and able to work in a structured and independent manner. Other Information If you are interested…

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…

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…

About the Company Our client is a global biopharmaceutical organization with a large manufacturing and supply chain operation in Breda. The site supports the production, packaging, storage and distribution of medicines to markets across Europe, Turkey, the Middle East and Africa, operating in a complex and highly regulated environment. Role Description As a Supply Chain – Detailed Scheduler, you will be responsible for managing short-term production planning for packaging lines and ensuring a stable and reliable supply of medicines. You will develop production plans, coordinate activities across departments and remove operational flow stoppers to support timely delivery. Working closely with manufacturing, quality, warehouse and supply chain teams, you will also contribute to continuous improvement, standardization and process automation within the supply planning organization. Key Responsibilities Manage short-term production planning for packaging lines. Create production plans, manage orders and support product launches and phase-in/phase-out activities. Monitor supply chain performance and proactively remove flow stoppers. Measure weekly and monthly KPIs, including MPS stability, and drive improvement actions. Facilitate daily operational meetings and coordinate actions across departments. Lead weekly capacity meetings with manufacturing,…

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…

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.…