Life Sciences Consultancy & Project Management in Netherlands

Over het bedrijf Onze opdrachtgever is een toonaangevende industriële organisatie met een complexe procurement- en maintenanceomgeving. De organisatie versterkt haar financiële controles en leveranciersprocessen om contractuele compliance, transparantie en effectieve spend management te waarborgen. Functieomschrijving Als Buyer – Contract & Spend Control beoordeel je complexe en risicovolle leverancierstransacties binnen een tijdelijk spend validation team. Je controleert Service Entry Sheets (SES), contracten en onderliggende documentatie, identificeert afwijkingen en financiële risico’s en onderbouwt je conclusies met feiten. Je werkt nauw samen met Procurement, Operations, Finance, Contract Management en leveranciers. Belangrijkste verantwoordelijkheden Valideren van SES-transacties aan de hand van contracten en commerciële afspraken. Controleren van tarieven, toeslagen, hoeveelheden, materialen en uitgevoerde werkzaamheden. Beoordelen van onderliggende documentatie en bewijsstukken. Identificeren van contractafwijkingen, financiële risico’s en compliance issues. Interpreteren van contracten en beoordelen van de praktische toepassing. Bespreken van bevindingen met leveranciers en interne stakeholders. Ondersteunen van reviewers bij complexe contractuele vraagstukken. Vastleggen van bevindingen en formuleren van feitelijk onderbouwde conclusies. Bijdragen aan rapportages en procesverbeteringen rondom spend control. Escaleren van complexe of risicovolle dossiers waar nodig. Vereisten HBO-opleiding in Inkoop, Bedrijfskunde, Supply Chain, Finance,…

Company Overview A leading biotechnology organization dedicated to developing innovative medicines that improve patient lives worldwide. With a diverse workforce of over 1,000 people from 38 countries, the company operates manufacturing, supply chain, marketing, and clinical research activities to serve millions of patients globally. Role Description We are seeking a proactive and detail-oriented Supply Chain Associate to join our Clinical Supply Operations team. In this role, you will support the end-to-end management of our clinical supply chain, ensuring the safe and timely delivery of investigational medicines to clinical sites across the globe. Responsibilities – Assist in managing the lifecycle of clinical supplies, from labeling and packaging to distribution and final disposal. – Support the coordination of product labeling, assembly, storage, and shipment activities in accordance with regulatory standards. – Collaborate with cross-functional teams including Regulatory Affairs, Manufacturing, and Clinical Operations to facilitate product launches and updates. – Maintain accurate documentation and track all supply activities within the relevant systems. – Support inventory management, tracking shipments, and resolving supply chain issues. – Participate in process improvement initiatives aimed at increasing efficiency…

About the Company: Our client is a leading pharmaceutical manufacturing company that produces high-quality medicines in a clean, modern, and highly regulated production environment. Safety, quality, teamwork, and continuous improvement are key priorities across the organisation. About the Role: We are looking for an Automated Production Technician to join a GMP-regulated manufacturing team. In this role, you will operate and monitor automated production equipment, help resolve technical issues, complete production documentation, and ensure products are manufactured safely and according to quality standards. You will work closely with colleagues from Production, Quality, Engineering, and Maintenance to keep the production process running smoothly and efficiently. Key Responsibilities: -Operate and monitor automated production equipment in accordance with GMP guidelines and standard operating procedures (SOPs). -Identify, troubleshoot, and report equipment or production issues. -Perform basic machine adjustments to support efficient production and minimise downtime. -Accurately record production data and activities in SAP and MES systems. -Monitor the manufacturing process and escalate deviations or quality concerns when required. -Complete production documentation, including batch records and production logs. -Support line setup, product changeovers, and shutdown activities.…

About the Company Our client is an international organization within the food industry, operating across multiple markets and product categories. Within a global Quality and Regulatory environment, the organization focuses on ensuring product compliance while supporting innovation and business growth. Role Description As a Regulatory Affairs Specialist, you will ensure compliance with food legislation and customer requirements across an international product portfolio. You will monitor regulatory developments, assess their business impact and advise stakeholders on practical solutions. Working closely with Quality, R&D, Supply Chain, Sales and Marketing, you will support product development, labeling, market introductions and regulatory projects. Key Responsibilities Monitor food legislation and regulatory developments and assess their impact. Review and approve labels, packaging, claims and communication materials. Provide regulatory guidance throughout product development and innovation projects. Conduct regulatory risk assessments and impact analyses. Advise stakeholders on food legislation and compliance requirements. Support the resolution of compliance issues and non-conformities. Contribute to regulatory policies, guidelines and process improvements. Support customer and market-related regulatory questions. Collaborate with international Regulatory Affairs and Quality teams. Develop expertise in areas such as packaging,…

The Company A leading pharmaceutical manufacturing organization with a strong focus on automation, quality, GMP compliance, and operational excellence. The company operates advanced production facilities where technology and continuous improvement are key to maintaining reliable manufacturing processes.   Role description As an Automated Line Operator, you will play an important role in keeping automated production and packaging operations running safely and efficiently. You will operate and monitor equipment, troubleshoot technical issues, maintain GMP standards, and support improvements across the production process. You will work closely with Production, Maintenance, Quality, and Engineering teams to maintain smooth operations and quickly respond to production challenges.   Responsibilities Operate and monitor automated production and packaging equipment Perform equipment setup, changeovers, and shutdown activities Monitor machine performance and production output Troubleshoot technical and process-related issues Adjust machine settings and parameters to maintain optimal performance Record production activities and data in SAP and MES Complete accurate GMP documentation and production records Identify and escalate deviations or abnormalities when required Support root cause analysis and structured problem-solving activities Work with Production, Quality, Maintenance, and Engineering teams to…

Company: A leading organization dedicated to food innovation and safety, committed to ensuring compliance with international food regulations while supporting product development and business growth. The company values scientific expertise, collaboration, and continuous improvement to deliver high-quality products to consumers worldwide. Job Description: We are seeking a knowledgeable Food Regulatory Affairs Expert to join our client’s team. This key role involves ensuring that products and business processes adhere to food legislation and internal policies across a global portfolio. The successful candidate will translate complex regulations into practical solutions, support innovation, and act as a trusted advisor across various departments. Responsibilities: – Monitor changes in food legislation, regulations, and industry standards; evaluate their impact on products and processes. – Review and approve product labels, packaging, claims, and communication materials to ensure compliance. – Provide regulatory guidance throughout the product development cycle, from concept to launch. – Conduct risk assessments for new ingredients, packaging changes, and legislative updates. – Advise colleagues in Sales, Marketing, Supply Chain, R&D, and Manufacturing on regulatory requirements. – Assist in resolving compliance issues by identifying risks and…