Senior Data Engineer, Utrecht, Utrecht

Company A leading public organization dedicated to ensuring the safety, accessibility, and sustainability of national infrastructure. They are involved in large-scale projects that contribute to maintaining and improving key transport connections and public assets across the Netherlands. Job Description We are seeking an experienced Senior Project Controls Coordinator to support the management of maintenance and renewal projects for bridges in Zeeland. This role involves establishing and maintaining effective project control processes, providing vital oversight, and ensuring projects are delivered on time, within scope, and within budget. The successful candidate will be instrumental in building the project controls framework from the ground up, contributing to the safe and efficient operation of bridge infrastructure. Responsibilities -Develop, implement, and oversee project control systems across multiple bridge maintenance and renewal projects. -Ensure accurate tracking and reporting of project scope, schedule, finances, risks, quality, and documentation. -Provide clear insights and highlight potential issues or blind spots within project controls. -Collaborate with project teams to establish aligned processes for planning, budgeting, risk management, and quality assurance. -Translate findings into actionable recommendations for decision-making. -Liaise with colleagues to maintain high standards of project control quality and timeliness. -Lead and motivate a team of professionals, fostering a culture of accountability and continuous improvement. -Build the project controls framework in a relatively new environment, setting up processes and workflows from scratch. -Monitor project performance, anticipate challenges, and implement corrective measures where needed. -Ensure all project control activities comply with applicable frameworks and organizational standards. Requirements -Minimum of 5 years’ experience in project control or management. -Relevant higher education qualification (HBO level) in finance, economics, or business administration. -Solid understanding of the IPM model and the role of project controls within infrastructure projects. -Proven ability to establish project control processes independently from the ground up. -Strong leadership skills and experience in managing project control teams. -Excellent analytical skills, with the ability to identify and address control gaps. -Effective communicator, capable of working across disciplines and levels of the organization. -Flexibility to work on-site in Middelburg every Tuesday and adapt to project needs. -Proficiency in Dutch language. 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 global pharmaceutical organization with a GMP manufacturing environment. The site Engineering organization supports technical projects that ensure reliable, compliant, and efficient manufacturing operations. Role Description As a CQV Engineer, you support technical projects from commissioning through qualification and validation. You develop and execute test strategies, prepare CQV documentation, and provide technical guidance to project teams to ensure systems meet customer requirements and GMP standards. Key Responsibilities Develop and maintain CQV documentation, including validation plans, risk assessments, protocols, and reports Lead commissioning, qualification, and validation activities Develop test strategies and execute qualification testing Support project teams with CQV and GMP guidance Ensure technical solutions align with validation requirements and procedures Track project activities, issues, and timelines Report progress and escalate issues when required Requirements Minimum 3 years of CQV experience within pharmaceutical manufacturing Hands-on commissioning and qualification experience in secondary packaging operations Experience with print and inspection systems, such as Systech or Cognex Experience with Computerized Systems Validation (CSV) Strong knowledge of GMP validation practices Experience developing validation and qualification documentation Good technical writing skills in English Strong communication and stakeholder management skills Able to work independently with limited supervision Strong analytical and problem-solving skills

The Company A global pharmaceutical manufacturing organization focused on delivering high quality healthcare products through advanced production technologies and strict regulatory compliance. The company operates in a highly regulated environment and emphasizes innovation, quality, operational excellence, and patient safety. Role description The Validation Engineer supports engineering and validation projects within a GMP regulated manufacturing environment. This role focuses on commissioning, qualification, and validation activities for secondary packaging systems and computerized systems. The position requires strong technical expertise, documentation skills, and the ability to work independently while ensuring compliance with established quality standards and procedures. Responsibilities - Develop and maintain validation documentation including criticality assessments, qualification plans, validation plans, risk assessments, test protocols, traceability matrices, and summary reports - Lead commissioning, qualification, and validation activities for manufacturing systems - Execute testing activities and document results according to GMP requirements - Support project teams to ensure technical solutions comply with validation plans and internal procedures - Provide technical guidance throughout project execution - Ensure documentation is complete, accurate, and inspection ready - Support project delivery through design, implementation, testing, commissioning, and validation phases - Complete additional assignments and projects as requested by management Requirements - Minimum 3 years of commissioning, qualification, and validation experience within pharmaceutical manufacturing - Experience with secondary packaging systems - Experience with print and inspection systems such as Systech and Cognex Knowledge of computerized systems validation - Hands on commissioning and qualification experience within secondary packaging operations - Strong understanding of validation lifecycle documentation - Experience working in a GMP regulated environment - Excellent technical writing skills in English - Strong communication and stakeholder management abilities - Critical thinking and problem solving skills - Ability to work independently with limited supervision - Strong project coordination and prioritization capability Other Information If you are interested and want to apply, please submit your application via the apply button below and contact me.

Job Vacancy — Project Controls Manager | Zeeland About the company A major Dutch public-sector organisation responsible for the development, management and maintenance of the Netherlands’ primary infrastructure. Its work covers major roads, waterways, bridges and other critical infrastructure, with a strong focus on safety, accessibility and long-term asset management. For its regional activities in Zeeland, our client is working on a range of infrastructure maintenance and renewal projects, including bridge projects currently underway and in preparation. About the position We are looking for an experienced Project Controls Manager to join a relatively new bridge-focused project cluster in Middelburg, Zeeland. In this role, you will be responsible for the integrated control of one or more infrastructure contracts. You will bring together planning, costs, risks, quality, scope and project information to give project teams a clear overview of progress and potential issues. A key part of the role is building structure. The project-control function is still being developed, so you will help establish processes, improve ways of working and ensure that reliable management information is available for decision-making. You will work within an Integrated Project Management (IPM) environment and collaborate closely with project managers, technical, contract and other project-control professionals. Hybrid working is possible, with Tuesday as the fixed team collaboration day in Middelburg. Responsibilities Lead the integrated project-control activities for infrastructure maintenance and renewal contracts. Monitor and connect scope, planning, budget, risks, quality and progress. Identify gaps, risks and dependencies and bring them to the attention of the project team. Translate project-control analysis into clear recommendations and decision-making information. Establish and improve project-control processes, structures and working methods. Coordinate different project-control disciplines, including planning, financial control, risk and quality management. Ensure project-control information and reporting are delivered accurately and on time. Provide direction to project-control professionals and encourage consistent ways of working. Work closely with the wider IPM team and relevant internal and external stakeholders. Help create a structured and reliable project-control environment within a developing project cluster. Requirements Minimum 5 years of professional experience in project controls / projectbeheersing. Completed HBO-level or higher education in a relevant field such as Finance, Economics, Business Administration or a comparable discipline. Demonstrable knowledge of the IPM model and the role of Project Controls Manager within an integrated project environment. Strong understanding of several project-control disciplines, such as planning, financial management, risk management and quality management. Experience working in complex projects, preferably within infrastructure, construction, maintenance or another technical environment. Strong analytical and organisational skills, with the ability to create structure from complex information. Able to take ownership, work independently and proactively identify areas for improvement. Strong communication and stakeholder-management skills. Fluent Dutch. Able to work onsite in Middelburg on Tuesdays, with additional onsite presence when required by the projects.

Company: Our client is a leading public organization responsible for maintaining the safety, accessibility, and sustainability of national infrastructure, including roads, waterways, tunnels, bridges, and flood defenses across the Netherlands. They focus on delivering large-scale projects that support the country’s vital transportation and water management systems. Job Description: We are seeking a dedicated Project Coordinator to support the Dredging & Salvage cluster within a major waterway maintenance program. The ideal candidate will provide crucial organizational, coordination, and administrative support to ensure smooth project operations and facilitate effective communication within the team. Responsibilities: Organize and coordinate meetings, workshops, and work sessions, including preparing agendas and gathering input. Manage calendars and assist with scheduling for project leaders and team members. Draft, distribute, and archive meeting minutes, reports, and decision documents. Monitor and follow up on actions, decisions, and deadlines to ensure timely progress. Support project management with organizational tasks such as preparing reports, memos, and presentations. Maintain the accessibility and organization of project documents and information flows using platforms like SharePoint and Microsoft 365. Facilitate internal communication by structuring and maintaining project files and updates. Assist in preparing periodic progress reports for management and stakeholders. Identify opportunities to improve work processes and contribute to a well-organized project environment. Serve as a point of contact within the team for procedural and informational issues, ensuring smooth information exchange and decision-making support. Requirements: Higher professional education (HBO) in a relevant field such as Public Administration, Business Administration, or Management Support. Minimum of 5 years’ proven experience in project coordination, supporting project teams, or similar roles within complex, multi-stakeholder environments. At least 3 years’ experience organizing and supporting intricate meetings, including agenda setting, minute-taking, and action tracking. Fluency in Dutch, both spoken and written, with strong skills in reporting and document creation. Proficiency in Microsoft 365, SharePoint, and digital collaboration tools. Ability to work independently, prioritize tasks, and proactively address organizational needs. Available to work on-site in Rotterdam on Tuesdays and Thursdays. 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 asset management organization committed to building a robust data-driven environment to support responsible AI and ensure trusted data practices across its operations. Job Description We are seeking an experienced Head of Data Governance and Data Architecture to lead the development and execution of data governance strategies within the organization. This key leadership role involves guiding a multidisciplinary team to establish a clear, scalable, and trustworthy data landscape that supports innovative AI initiatives and compliance. Responsibilities - Lead the team responsible for implementing and operationalizing data governance frameworks across the organization. - Develop and embed governance foundations to ensure data is well-defined, owned, traceable, and of high quality, supporting responsible AI use. - Connect established data governance practices with AI governance needs, including data ownership, lifecycle management, metadata, lineage, quality, and oversight. - Collaborate closely with senior stakeholders such as Data Owners, Data Stewards, AI Leads, Business Owners, Data Management, and Legal teams to create clarity and alignment. - Ensure data architecture supports governance outcomes and aligns with enterprise standards and decisions. - Oversee aspects of data architecture and modelling, ensuring they support governance objectives. - Drive a transformation from fragmented data practices towards a transparent, scalable, and governed data environment. - Lead a team with expertise in data governance, metadata, data quality, business analysis, architecture, and modelling. Requirements - Proven experience in leading data governance and data architecture initiatives. - Strong understanding of data quality, metadata management, and data lifecycle controls. - Experience supporting AI governance and responsible data use. - Ability to work strategically and practically, guiding teams and stakeholders effectively. - Excellent leadership and collaboration skills, with experience working with senior management. Other Information If you are interested and want to apply, please submit your application via the apply button below and contact me.

Company Overview: Our client is a global leader in animal health, committed to improving the well-being of animals and supporting the world’s food supply. They operate within a high-tech, innovative environment that develops and produces veterinary medicines. Their site in Boxmeer is part of an international network and specializes in the manufacturing and packaging of vaccines and medicines for a wide range of livestock and companion animals. Their production teams focus on vaccine development, viral and bacterial antigen production, working under strict GMP and EHS standards to ensure the highest quality and safety. Job Description: We are seeking an experienced Senior Bioprocess Technician to join their dynamic team in the Bioreactor Facility at the Boxmeer site. In this role, you will be responsible for supporting large-scale biotechnological production processes for animal vaccines, ensuring smooth operation, compliance, and continuous improvement within a high-tech environment. Responsibilities: Prepare production cultures and media meticulously for each production cycle Independently execute complex production tasks, including cell and virus culture management, fermenter control, centrifugation, filtration, and vessel handling Document all production activities precisely, ensuring batch records are complete and accurate Follow strict GMP and EHS guidelines and observe all safety and quality regulations Identify, report, and document deviations or issues in the production process Contribute to process improvement initiatives and participate in project teams Support deviation management through thorough documentation of any process variations Lead or participate in troubleshooting and technical tasks related to process control systems and mechanical aspects such as valves and fittings Train and mentor colleagues through knowledge transfer and on-the-job training Assist in organizational and logistical improvements to optimize production flow Support on-call and weekend shifts, with potential for future shift work or rotation Requirements: MBO level 3 or 4 in Biotechnology, Process Technology, or a related field Previous experience in bioprocessing, ideally within animal health or pharmaceutical manufacturing (entry-level candidates are encouraged to apply) Familiarity with aseptic techniques and working in controlled environments such as cleanrooms or biosafety cabinets (applicants with limited experience are encouraged to apply) Technical interest in virology, bacteriology, microbiology, and process technology, with willingness to undergo further training Strong understanding of process trending and change management High awareness of quality and safety standards Stress-resilient with good prioritization skills Excellent communication skills in Dutch and English Team-oriented with a proactive approach 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 an international manufacturing company operating in a highly regulated production environment. The organisation uses advanced automated manufacturing and packaging technologies to deliver high-quality products while maintaining strong standards for safety, compliance, and operational excellence. The site values teamwork, continuous improvement, technical expertise, and innovation. Job Description We are looking for a Manufacturing Operator (GMP) to join a dynamic production team. In this role, you will help keep semi-automated production and packaging lines running safely, efficiently, and according to GMP requirements. You will monitor equipment, handle basic technical issues, complete production activities, and support the team in keeping production running smoothly. Roles & Responsibilities - Run and monitor semi-automated production and packaging lines in a GMP environment. - Set up and start production equipment according to SOPs and production instructions. - Check and adjust machines and process settings when needed. - Carry out cleaning, product changeovers, line clearance, and basic equipment checks. - Identify and troubleshoot machine or process issues to reduce production downtime. - Make basic machine adjustments to keep the production process running smoothly. - Record and verify production information in SAP, MES, and other manufacturing systems. - Complete batch records, equipment logs, and other production documentation accurately. - Check product quality during production and report deviations or abnormalities. - Perform first-line checks and basic maintenance when required. - Follow GMP, SOPs, safety rules, and site procedures at all times. - Coordinate with Production, Maintenance, and Quality teams to resolve technical or production issues. - Support root cause investigations using methods such as 5 Why and RCA. - Contribute to continuous improvement initiatives using Lean and Kaizen principles. - Communicate clearly during shift handovers and share relevant production information with colleagues. Requirements - Technical education at MBO level or an equivalent qualification such as VAPRO B. - Experience in automated production, assembly, packaging, or process manufacturing. - Good technical understanding and the ability to identify and solve production issues. - Familiarity with RCA, 5 Why, Lean, or Kaizen is an advantage. - Experience in GMP or another regulated manufacturing environment is highly desirable. - Knowledge of SAP, MES, or similar production systems. - Good communication skills in English. - Willingness to work rotating 3-shift and 5-shift schedules. - Available for a temporary full-time contract (1 year). Why Apply? This role is a great opportunity for someone who enjoys working with modern manufacturing technology and solving technical production challenges. If you're ready for your next challenge in automated manufacturing, we'd love to hear from you. Apply today by clicking the application button below or contact me directly for more information.

Company Our client is a global organization active in animal health, developing and manufacturing innovative veterinary medicines and vaccines for worldwide distribution. The Boxmeer site is a high-tech production location operating under strict quality and safety standards, where teams work in an international environment with a strong focus on continuous improvement. Job Description For our client in Boxmeer, we are looking for a Bioprocess Manufacturing Technician to support large-scale cell and virus culture processes used to produce vaccine antigens. This role is hands-on in a GMP-regulated manufacturing environment and focuses on executing and coordinating production activities safely, accurately, and within planned timelines. The Bioreactor Operations Technician also contributes to improvement initiatives to optimize processes and ways of working. Responsibilities - Prepare and support production runs, including culture preparation and media preparation - Execute production activities in a complex bioprocess environment, such as: Cell culture and virus culture, Inactivation steps, Operating and monitoring bioreactors/fermenters, Working with centrifuges, filtration systems, vessels, and single-use bioreactor equipment - Record all activities accurately and complete batch documentation in line with procedures - Work strictly according to GMP and EHS requirements in classified/controlled areas - Identify, report, and help investigate deviations; contribute to accurate deviation documentation - Support continuous improvement by proposing and driving process and workflow optimizations - Share knowledge within the team through training-on-the-job and daily collaboration - Participate in project groups focused on process and supporting-process improvements - Support production trending and help assess process performance over time - Be flexible to support on-call duties and occasional weekend work, with the possibility of shifted working patterns in the future Requirements - Completed vocational education (MBO level 3/4) in Biotechnology, Process Technology, or similar - Interest in bioprocessing within a regulated manufacturing environment (GMP) - Experience in aseptic/controlled environments (e.g., cleanroom or biosafety cabinet) is a plus, but starters are also welcome - Affinity with virology, bacteriology, microbiology, and/or pharmaceutical manufacturing techniques - Strong quality and safety mindset; able to follow procedures and work accurately - Able to stay calm under pressure and set priorities - Good communication skills in Dutch and English - Team player with a proactive, hands-on attitude Other Information This position is based on-site in Boxmeer, Netherlands. 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 Nederlandse overheidsorganisatie die verantwoordelijk is voor veilige, bereikbare en goed onderhouden infrastructuur in Nederland. Binnen de afdeling Programma's, Projecten en Onderhoud is het cluster Baggeren & Berging verantwoordelijk voor het onderhoud van vaarwegen en bergingswerkzaamheden langs de Nederlandse kust. Functieomschrijving Als Clustercoördinator ben je het centrale aanspreekpunt voor de organisatie en coördinatie binnen het cluster. Je ondersteunt de Projectmanager, Projectcontrolmanager en het IPM team door structuur te creëren, informatiestromen te coördineren, overleggen en besluitvorming voor te bereiden en acties op te volgen. Je werkt zelfstandig binnen een complexe en multidisciplinaire projectomgeving. Belangrijkste verantwoordelijkheden Organiseren en coördineren van overleggen, workshops en bijeenkomsten Voorbereiden van agenda's, vergaderstukken, rapportages en presentaties Notuleren en beheren van actie- en besluitenlijsten Bewaken van acties, deadlines en gemaakte afspraken Ondersteunen van de Projectmanager en het IPM-team bij coördinatie en rapportage Beheren van projectdocumentatie en informatiestromen Opstellen en coördineren van memo's, nota's en managementrapportages Signaleren van procesverbeteringen en bijdragen aan de uitvoering hiervan Vereisten HBO-opleiding in een relevante richting, zoals Bestuurskunde, Bedrijfskunde, Communicatie of Management Support Minimaal 5 jaar ervaring als Projectsecretaris, Projectcoördinator, Clustercoördinator of vergelijkbaar Ervaring binnen een complexe project- of programmaomgeving Minimaal 3 jaar ervaring met het ondersteunen van complexe overleggen en besluitvorming Uitstekende beheersing van de Nederlandse taal, mondeling en schriftelijk Ervaring met Microsoft 365, Teams en SharePoint Sterke organisatorische en communicatieve vaardigheden Proactief, nauwkeurig, zelfstandig en samenwerkingsgericht Beschikbaar op dinsdag en donderdag op locatie in Rotterdam