Life Sciences Consultancy & Project Management in Netherlands
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Whether you are a life sciences organisation looking to strengthen your project and consultancy capabilities or a specialist seeking new opportunities, SIRE Life Sciences provides the expertise, data, and network to make success inevitable. We connect specialist life sciences consultants with projects that drive discovery, production, and healthcare innovation across the Netherlands. that drive discovery, production, and healthcare innovation across the Netherlands. Join the companies and professionals shaping the future of biotechnology, pharmaceuticals, and medical innovation. Empowering Life Sciences through People, Projects, and Performance.
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Project Controls Manager
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…
CQV Engineer
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…
Validation Engineer
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…
Project Controls Manager
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…
Senior Data Engineer
About the Company Join a leading international financial services organization where data, technology, and innovation drive business transformation. You will work within a technology-focused engineering environment, contributing to strategic data products that provide trusted insights and support enterprise-wide decision-making. Role Description We are looking for a Senior Data Engineer (Azure Synapse & Databricks) to support the development, optimization, and future evolution of enterprise data products. You will play a key role in enhancing existing solutions, building scalable data pipelines, and supporting the transition towards a modern Databricks-based platform. Responsibilities – Design, develop, and optimize data pipelines using Azure Synapse and Databricks. – Build scalable ELT/ETL frameworks and reusable data components. – Develop and maintain APIs and data products. – Improve data quality, reliability, performance, and maintainability. – Support platform modernization and migration initiatives. – Collaborate with Business Analysts, Architects, Product Owners, and engineering teams. – Contribute to CI/CD processes, testing, monitoring, and automation. – Drive knowledge transfer and reduce technical debt. Requirements – 5+ years of experience as a Data Engineer. – Strong experience with Azure Synapse Analytics and Azure…
Project Coordinator
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…
SIRE® Life Sciences
SIRE® Life Sciences is a leading partner in project management, consultancy and secondment services for the Life Sciences industry in the Netherlands. With a proven track record of excellence, we provide strategic workforce and project solutions that empower Life Sciences organizations across biotechnology, pharmaceuticals, clinical research, medical devices, and the food industry to achieve operational success and sustainable growth.
Our team of Life Sciences specialists combines scientific expertise with business insight to deliver customized project management, consultancy, and secondment services that align with the highest standards of quality and compliance. We support Life Sciences clients through every phase of the product lifecycle; from research and development (R&D) to clinical trials, manufacturing, and commercialization.
As the leading Life Sciences consultancy in the Netherlands, we have a strong network of exceptional consultants in areas such as biotech engineering, clinical operations, regulatory affairs, pharmacovigilance, manufacturing, quality assurance and medical affairs. Our consultants and project managers bring deep industry knowledge and a results-driven mindset, ensuring each project is delivered on time, within scope, and in full compliance with international standards.