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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Platform Architect
The Company Our client is one of the Netherlands’ leading financial institutions, with a strong presence in banking and a large-scale technology environment supporting critical financial services. The organisation is committed to innovation, security and resilience, continuously investing in modern technology platforms and secure digital solutions. Job Description As a Platform Architect, you will shape the architecture and roadmap for critical IT platform services across Linux, Windows, storage, backup, disaster recovery and cyber resilience. You will work closely with Engineering, Security and senior stakeholders, guiding Solution Architects and translating business, security and regulatory requirements into scalable, secure and resilient technology solutions. Responsibilities Develop and maintain the architecture blueprint for Platform Services, including operating systems, storage, backup, disaster recovery, and cyber resilience. Collaborate with stakeholders to translate business needs and regulatory demands into detailed technical strategies. Provide architectural guidance on Linux, Windows, SAN, NAS, object storage, and archiving solutions. Lead the design of backup, restore, disaster recovery, and cyber recovery strategies, balancing security, operational complexity, and costs. Co-lead the Platform Services area alongside the Area Lead and Tech Lead, providing strategic direction.…
LIMS Specialist
The company Our client is a global biopharmaceutical organisation committed to advancing innovative medicines that improve patients’ lives worldwide. Through advanced research, biologics manufacturing, and a strong focus on quality and innovation, the organisation delivers life-changing therapies across a wide range of therapeutic areas. Role Description As a LIMS Specialist, you will play a key role in the implementation, maintenance, and digitalisation of laboratory methods within a regulated Quality Control environment. You will focus on LIMS method templates, master data, validation, and the harmonisation of paper-based laboratory methods into digital workflows. You will also support laboratory teams with digital processes, instrument interfaces, and LIMS-related activities. Responsibilities – Lead the harmonisation and digitalisation of paper-based laboratory methods within a regulated QC environment. – Create, configure, and maintain method execution templates, master data, and digital laboratory methods in LIMS. – Support validation activities, change controls, and technical documentation related to digital laboratory processes. – Manage updates and improvements to existing digital methods in collaboration with laboratory SMEs and other sites. – Support the setup, testing, and validation of LIMS-to-instrument interfaces and related…
LIMS Specialist
The Company The client is part of the global pharmaceutical company. The facility is focused on the development and manufacturing of biologic medicines, particularly in the fields of immunology, oncology, and infectious diseases. They specialize in producing large-scale biologic drugs, which are typically made from living cells and are used to treat complex diseases. Role Description We are seeking an experienced LIMS Specialist to support the deployment, optimization, and ongoing maintenance of digital laboratory solutions within the Advanced Therapies Quality Control (QC) organization. Based in Leiden, the successful candidate will act as the key expert for paperless laboratory implementation, partnering closely with local method SMEs and cross-functional teams to transform paper-based laboratory processes into standardized digital workflows. This position plays a critical role in driving digitalization initiatives, ensuring alignment with global standards, supporting system harmonization across sites, and enabling efficient execution of laboratory methods within the LIMS environment. Responsibilities Lead the conversion of paper-based laboratory methods into standardized digital workflows and execution templates. Drive harmonization initiatives to ensure consistency of laboratory methods and processes across multiple sites. Develop, maintain, and update method execution templates…
Technical Operator – Semi-Automated Lines
About the Company Join a leading international pharmaceutical manufacturer where medicines are labeled, assembled, stored, and distributed worldwide. Working in a GMP-regulated production environment, you will help ensure reliable manufacturing processes while contributing to product quality and continuous improvement. Role Description As a Technical Operator – Semi-Automated Lines, you will operate and monitor semi-automated production equipment to ensure safe, efficient, and compliant manufacturing. You will perform machine set-ups, troubleshoot production issues, maintain accurate documentation, and support continuous improvement initiatives within a structured production environment. Key Responsibilities Operate and monitor semi-automated production and packaging lines Perform machine set-ups, changeovers, line clearances, and cleaning activities Troubleshoot equipment and process issues and perform minor machine adjustments Record production activities and batch data in SAP and MES systems Support deviation investigations and production triage activities Contribute to Lean and Continuous Improvement initiatives Ensure compliance with GMP, safety, and quality standards Follow SOPs and work instructions to maintain efficient production Support optimal equipment performance and production reliability Requirements MBO degree or equivalent technical background Experience operating production, assembly, labeling, or packaging equipment Technical understanding of…
Technical Operator – Automated Lines
About the Company Join a leading international pharmaceutical manufacturer where medicines are labeled, assembled, stored, and distributed worldwide. Working in a highly automated GMP manufacturing environment, you’ll help ensure reliable production while contributing to continuous improvement and operational excellence. Role Description As a Technical Operator – Automated Lines, you will operate, monitor, and optimize fully automated production equipment to ensure safe, efficient, and compliant manufacturing. You will play an important role in troubleshooting technical issues, improving equipment performance, and maintaining high quality standards within a regulated production environment. Key Responsibilities Operate and monitor fully automated production and packaging lines Perform machine set-ups, changeovers, line clearances, and cleaning activities Troubleshoot equipment and process issues using structured problem-solving methods Perform minor maintenance and mechanical or parameter adjustments Record production activities and batch data in SAP and MES systems Support deviation investigations and production triage activities Perform Root Cause Analyses (RCA, 5 Why) and implement corrective actions Contribute to Lean and Continuous Improvement initiatives Ensure compliance with GMP, safety, and quality requirements Support optimal equipment performance and production efficiency Requirements MBO degree or…
LIMS Subject Matter Expert
The Company Our client is a global biopharmaceutical company committed to advancing innovative medicines that improve patients’ lives worldwide. Through cutting-edge research, advanced biologics manufacturing, and a strong focus on quality and innovation, the company delivers life-changing therapies across a wide range of therapeutic areas. Role Description The LIMS Subject Matter Expert will lead the implementation and maintenance of digital laboratory methods within a regulated QC environment. The role focuses on LIMS method templates, master data, validation, paper-to-digital method harmonization, and supporting laboratory teams with digital workflows and instrument interfaces. Responsibilities Lead the harmonization and digitalization of paper-based laboratory methods within a regulated QC environment. Create and maintain method execution templates, master data, and digital methods in LIMS. Support validation activities, change controls, and technical documentation for digital laboratory processes. Manage updates to existing digital methods and coordinate with laboratory SMEs and other sites. Support the setup and validation of LIMS–instrument interfaces and related digital workflows. Provide training and act as the main point of contact for laboratory users on digital methods and LIMS-related questions. Requirements Bachelor’s degree or equivalent…
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.