Platform Services Architect, Utrecht, Utrecht

The Company A leading international industrial manufacturing organization with large scale operations and a strong focus on operational excellence, asset reliability, and procurement governance. The organization is currently investing in enhanced financial control, contract compliance, and risk management initiatives to strengthen transparency and ensure proper application of supplier agreements and payment processes. Role description We are seeking an experienced Procurement Specialist to join a temporary Spend Validation Team focused on reviewing and validating supplier related transactions and contract compliance activities. In this role, you will assess high value and complex Service Entry Sheet transactions, investigate commercial and contractual deviations, identify financial risks, and provide fact based recommendations. You will work closely with Procurement, Finance, Operations, Contract Management, suppliers, and senior stakeholders. Responsibilities - Review and validate Service Entry Sheet transactions against contractual agreements - Verify rates, quantities, materials, surcharges, and completed work - Analyze supporting documentation and evidence for transaction approval Investigate discrepancies, compliance concerns, and financial leakage risks - Interpret supplier contracts and assess correct commercial application - Communicate with suppliers, contract owners, operational teams, and stakeholders - Support reviewers on complex contractual and commercial cases - Escalate high risk findings to senior specialists and leadership teams - Document findings and provide evidence based conclusions - Contribute to process improvement initiatives and spend control measures - Assist with reporting, analysis, and risk management activities - Support a transparent and controlled payment process Requirements - HBO degree in Purchasing, Business Administration, Supply Chain Management, - - Finance, Commercial Economics, or a related field - Minimum 4 years of relevant experience - Experience in procurement, supplier management, contract management, or commercial controls - Strong contract interpretation and analytical skills - Experience reviewing financial, commercial, or contractual documentation - Strong risk awareness and control mindset - Ability to independently assess complex situations and make informed decisions - Strong stakeholder management and communication skills - Experience in industrial or technical environments is advantageous - Knowledge of SAP is preferred - Experience with Service Entry Sheet processes is highly desirable - Experience with compliance, audit, assurance, or control environments is advantageous - Fluent in Dutch and English - NEVI certifications are considered an advantage 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 financial institution in the Netherlands supporting critical banking services through a large and sophisticated technology environment. The organization is committed to investing in secure, resilient, and modern technology platforms to ensure seamless service delivery in a highly regulated setting. Role Description We are looking for a Senior Platform Architecture Specialist to define and drive the future architecture of our IT platform services. You will translate business, security, regulatory, and technical requirements into practical architecture strategies and roadmaps, with a focus on stability, security, scalability, and resilience. Responsibilities - Develop and maintain the Platform Services architecture and roadmap. - Translate business and security requirements into practical technical solutions. - Define strategies for Linux, Windows, storage, backup, and disaster recovery. - Develop cyber resilience and system recovery strategies. - Guide Solution Architects and technical teams across multiple squads. - Ensure architecture follows security, enterprise, and regulatory standards. - Advise Engineering, Security, and Senior Management on architecture decisions. - Drive standardisation, modernisation, and continuous improvement of platform services. Requirements - Master’s degree or equivalent professional experience. - Extensive experience in IT infrastructure and architecture. - Strong experience in Enterprise, Solution, Platform, or Infrastructure Architecture. - Strong knowledge of Linux and Windows. - Expertise in storage, backup, disaster recovery, and cyber resilience. - Experience with on-premises, cloud, and hybrid environments. - Strong communication and stakeholder-management skills. - Pragmatic, solution-oriented approach with the ability to influence without formal authority. - Fluent in English and Dutch. - Experience in a highly regulated environment, such as financial services, is a plus. Other Information If you are interested and want to apply, please submit your application via the apply button below and contact me.

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, Commerciële Economie of vergelijkbaar. Ervaring binnen procurement, contractmanagement, leveranciersmanagement of contractcontrole. Ervaring met het interpreteren van contracten en leveranciersafspraken. Sterke analytische vaardigheden en oog voor detail. Ervaring met commerciële, financiële of contractuele vraagstukken. Sterk risico- en controlbewustzijn. Zelfstandig complexe dossiers kunnen beoordelen en onderbouwde conclusies kunnen trekken. Sterke communicatieve en stakeholdermanagementvaardigheden. Goede beheersing van Nederlands en Engels. Ervaring met SAP/SES is een sterke pré. NEVI 1/2 of relevante opleiding/certificering in inkoop, contractmanagement of supply chain is een pré. Ervaring binnen een industriële of technische omgeving is een voordeel.

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 and quality. - Manage specialized shipping requests, ensuring compliance with customs and safety regulations. - Assist with end-of-life activities for clinical trial materials and SKUs as needed. - Contribute to team projects by gathering data, preparing reports, and supporting stakeholder communication. Requirements - Bachelor’s degree or higher, preferably in a relevant field. - At least 2 years of experience in supply chain operations, preferably within the pharmaceutical or healthcare sector. - Fluency in English, both spoken and written. - Strong communication and organizational skills. - Experience working in an international or global supply chain environment. - Knowledge of regulatory standards related to clinical supplies is a plus. - Analytical mindset with good attention to detail. - Customer-focused, proactive, and capable of working independently as well as part of a team. - Tech-savvy with proficiency in supply chain systems and tools. 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 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. -Carry out routine cleaning and basic maintenance tasks according to procedures. -Work closely with Production, Quality, Engineering, and Maintenance teams to resolve operational issues. -Participate in shift handovers and communicate important production updates. -Contribute to process improvements that enhance safety, quality, and operational performance. -Maintain a clean, safe, and organised working environment always. Requirements: -Experience working in a manufacturing, production, or operations environment. -Experience operating automated machinery or production equipment. -Experience within a GMP-regulated environment is preferred, ideally within pharmaceuticals, -biotechnology, food, or another regulated industry. -Comfortable following procedures, work instructions, and documentation requirements. -Good technical aptitude and problem-solving skills. -Ability to work effectively within a team environment. -Good communication skills and a good command of English, both written and spoken. -Willingness to work shifts as required. -Familiarity with production documentation and GMP working practices. Other Information: If you are interested in this opportunity and your experience matches the requirements, please apply using the Apply button or contact me directly for a confidential discussion about the role.  

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, sustainability, nutrition and food claims. Requirements Bachelor's or Master's degree in Food Technology, Food Science, Nutrition, Chemistry or a related field. Minimum 5 years of relevant Regulatory Affairs experience. Strong experience with food legislation and regulatory compliance. Proven experience within the dairy industry. Experience working in a B2B environment. Strong ability to translate legislation into practical business solutions. Excellent stakeholder management and communication skills. Analytical, proactive and able to work independently. Comfortable working across international and cross-functional teams. Fluent in English; German is a plus.

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 resolve issues Identify opportunities to reduce downtime and improve equipment performance Support Lean Manufacturing, Kaizen, and continuous improvement initiatives Perform scheduled cleaning activities and ensure effective shift handovers Maintain a safe, clean, and GMP-compliant working environment   Requirements - Minimum 3 years of experience in manufacturing or production - Experience operating automated production or packaging equipment - Background in pharmaceutical, food, assembly, packaging, or similar industries - Fluent English communication skills - Experience working with GMP documentation and procedures - Strong troubleshooting and problem-solving skills - Experience with SAP and MES systems - Knowledge of Lean Manufacturing and continuous improvement - Willingness to work a rotating 3-shift or 5-shift schedule   Other Information If you enjoy working with automated technology, solving technical challenges, and improving production performance, this could be a great opportunity to put your skills into practice. Please submit your application via the Apply button below and contact me if you would like to discuss the opportunity.

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 developing practical solutions. - Support the creation and implementation of policies, guidelines, and standards to strengthen compliance. - Deliver training sessions to raise regulatory awareness within the organization. - Collaborate with international colleagues to ensure compliance in a complex business environment. - Develop expertise in specific areas such as sustainability, contaminants, nutrition, or food claims and serve as a trusted resource internally. Requirements: - Minimum of 5 years’ experience in food or dairy industry compliance and regulation. - Proven track record in a B2B environment with strong analytical and proactive skills. - Ability to communicate complex regulatory information clearly and pragmatically. - Experience working in cross-functional teams with a collaborative mindset. - Fluent in English; German language skills are a plus. - Comfortable working in a hybrid environment with some office presence. 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 dedicated to delivering high-quality food products, committed to compliance, innovation, and sustainability. The company operates within a complex, international environment, collaborating across various functions to ensure products meet all regulatory standards and customer expectations. Role Description We are seeking a Regulatory Affairs Specialist to join our client’s dynamic team. In this role, you will ensure that all products and processes comply with food legislation, internal policies, and customer requirements on a global scale. You will work closely with teams across R&D, Quality, Supply Chain, Sales, and Marketing to facilitate innovation while maintaining compliance. Responsibilities - Monitor global food legislation, regulations, and industry standards, evaluating their impact on the business. - Review and approve product labels, packaging, claims, and communication materials to ensure regulatory compliance. - Provide regulatory guidance during product development and innovation projects, from initial concept to launch. - Conduct risk assessments and impact analyses for new products, ingredients, packaging changes, and legislative updates. - Advise internal teams on regulatory requirements and support resolution of compliance issues by identifying risks and developing practical solutions. - Contribute to creating and updating policies, standards, and processes to strengthen compliance across the organization. - Deliver training sessions to raise regulatory awareness within the company. - Collaborate with international colleagues to ensure compliance across different markets. - Develop expertise in areas such as sustainability, contaminants, packaging, nutrition, and food claims, becoming a trusted internal advisor. Requirements - Minimum of 5 years’ experience in food regulation, ideally within the dairy industry. - Proven experience working in a B2B environment. - Strong understanding of food legislation and compliance processes. - Excellent communication skills in English; German language skills are a plus. - Analytical, proactive, and capable of working effectively in cross-functional teams. - Ability to interpret complex regulations and develop pragmatic, business-friendly solutions. Other Information If you are interested and want to apply, please submit your application via the apply button below and contact me.

The Company A global food and dairy organization operating across multiple international markets. The business focuses on delivering high quality food products while maintaining strong compliance, quality, and regulatory standards throughout the product lifecycle. The organization works closely with customers in a Business to Business environment and emphasizes innovation, product development, sustainability, and food safety compliance. Role description As a Regulatory Affairs Specialist, you will ensure compliance of food products, labels, packaging, and business processes with international food legislation and customer requirements. You will act as a trusted advisor to stakeholders across Quality, Research and Development, Supply Chain, Sales, and Marketing. This position combines regulatory expertise, business partnering, and project support, helping the organization translate complex legislation into practical business actions while supporting innovation and market expansion. Responsibilities Monitor global food legislation, regulatory developments, and industry standards Assess compliance risks and business impact of legislative changes Review and approve product labels, packaging artwork, and marketing claims Support innovation and product development projects from concept to launch Conduct regulatory impact assessments for ingredients, products, and packaging changes Advise internal stakeholders on food regulations and compliance requirements Support market expansion activities by evaluating regulatory requirements in different countries Investigate compliance issues and develop practical corrective solutions Develop and improve regulatory policies, guidelines, and internal processes Deliver regulatory training and awareness sessions to business teams Collaborate with international regulatory affairs colleagues Act as a subject matter expert in areas such as packaging, sustainability, contaminants, nutrition, and food claims Respond to regulatory and compliance questions from customers Support manufacturing transfer and cost reduction projects from a regulatory perspective Requirements Minimum 5 years of Regulatory Affairs experience Strong experience within the dairy industry Experience working in a Business to Business environment Degree in Food Science, Regulatory Affairs, Nutrition, Quality, or a related field Deep understanding of European and international food legislation Experience reviewing labels, claims, and packaging compliance Strong risk assessment and problem solving skills Ability to translate legislation into practical business actions Experience working in cross functional project teams Excellent stakeholder management skills Strong communication skills in English German language skills are advantageous Able to work independently with minimal supervision Experience supporting commercial and innovation projects Other Information If you are interested and want to apply, please submit your application via the apply button below and contact me.