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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Automation Operator
The Company A global pharmaceutical manufacturing organization focused on innovation, quality, and operational excellence. The company operates highly automated production facilities within a GMP regulated environment and invests heavily in advanced manufacturing technologies and continuous improvement initiatives. Role Description As an Automation Operator, you will be responsible for operating, monitoring, and optimizing automated production lines to ensure safe, efficient, and compliant manufacturing processes. This role combines technical troubleshooting, equipment operation, and GMP documentation while supporting process improvements and production performance. Responsibilities – Operate and monitor automated production equipment according to SOPs and GMP standards – Perform troubleshooting and root cause analysis on automated systems – Adjust machine parameters and settings to improve operational performance – Record and verify production data within SAP and MES systems – Monitor process performance and report deviations when required – Complete batch records, production logs, and GMP documentation accurately – Participate in cross functional problem solving and triage meetings – Execute equipment startup and shutdown procedures – Perform routine cleaning activities according to production schedules – Identify and support continuous improvement opportunities – Contribute to…
Cell Therapy Manufacturing Associate
Company Our client is an international life sciences organisation operating in a highly regulated environment. They develop and manufacture innovative therapies and are committed to high standards in quality, compliance, and continuous improvement. The working environment is dynamic, fast-paced, and strongly focused on teamwork and operational excellence. Job Description For a manufacturing site in Hoofddorp, we are looking for a GMP Cell Therapy Production Specialist to support the production of clinical and commercial cell therapy products in a cleanroom setting. This role sits within either the production team or the production support team and is focused on safe, compliant execution of manufacturing activities, accurate documentation, and proactive support of process improvements. Responsibilities The GMP Cell Therapy Production Specialist will be responsible for: – Executing manufacturing and/or production support activities in a GMP-regulated cleanroom environment (including aseptic areas). – Following SOPs and cGMP requirements and completing batch records accurately and on time. – Performing activities such as material preparation, material decontamination, and transferring materials and documentation into cleanroom areas. – Supporting aseptic processing steps and ensuring consistent process execution to meet…
Cell Therapy Manufacturing Specialist
The Company A leading organization in the biotechnology and advanced cell therapy sector focused on developing and manufacturing innovative treatments. The company operates in a highly regulated GMP environment with a strong emphasis on quality, patient safety, process excellence, and continuous improvement. Role Description This position supports the manufacturing of clinical and commercial cell therapy products within a GMP regulated environment. Successful candidates will be assigned to either the Production Team or Production Support Team after completing initial training requirements. The role requires hands on manufacturing activities, strict adherence to SOPs and GMP standards, and close collaboration with multiple operational and quality functions. Responsibilities – Perform apheresis accession and transfer to manufacturing areas – Complete batch records according to SOPs and GMP requirements – Support batch documentation review for product release activities – Supply manufacturing suites with required materials and components – Transfer batch records and documentation into cleanroom environments – Conduct final product visual inspections – Perform cryopreservation of excess cells and final product – Submit manufacturing samples to Quality Control – Manufacture clinical and commercial products in Grade…
Manufacturing Operations Specialist
Company Our client is an international pharmaceutical and biotechnology organization with a modern manufacturing facility in Breda. The site combines advanced production technology with strict GMP, quality, and safety standards. Job Description As a Manufacturing Operations Specialist, you will help ensure that manufacturing and packaging equipment performs reliably throughout the production process. You will prepare equipment for production, respond to operational issues, complete required documentation, and contribute to maintaining a safe and efficient manufacturing environment. Responsibilities – Keep manufacturing and packaging equipment running efficiently throughout production. – Prepare machines for different production runs, including set-ups, changeovers, line clearance, and shutdown activities. – Identify equipment or process issues and carry out first-line troubleshooting. – Perform minor machine adjustments to restore or improve equipment performance. – Complete GMP and production documentation accurately and on time. – Carry out required equipment and production-area cleaning activities. – Follow established GMP, SOP, quality, and safety procedures. – Identify recurring production issues and contribute to reducing downtime and improving efficiency. – Escalate complex technical problems to the appropriate technical specialists. – Collaborate with production,…
QC Microbiology analyst
The company Our client is a leader in immunotherapy and engineered T cell therapy, driving innovation in cancer treatment. They are transforming the landscape with personalized, patient-specific therapies. Role Description As a QC Microbiology Analyst, you’ll be part of a diverse team of 20+ Analysts, Senior Analysts, and Lead Analysts, reporting to one of the Team Leads in QC Microbiology. Your role involves performing various microbiological assays, environmental monitoring of cleanrooms, data entry and review, and supporting department projects in a fast-paced, collaborative work environment. Knowledge of GMP, aseptic techniques, and microbiological processes are essential for success. Responsibilities – Perform environmental monitoring of cleanrooms. – Conduct microbiological assays such as Gram Stain, Endotoxin, Sterility, Microbial Identification, Growth Promotion, Bioburden, and Plate Reading. – Data entry, review, and trending of assay results. – Perform routine maintenance of lab equipment and lab spaces. – Support department projects. Requirements – MLO level 4 (Vocational Training) or a Bachelor’s degree in Microbiology preferred. – 0 to 4 years of Microbiology lab/Environmental Monitoring experience. – Experience with microbiological techniques such as air monitoring, water testing,…
Automated Production Systems Technician
The Company A leading global biotechnology organization, dedicated to developing and delivering innovative medicines to improve patient outcomes. Operating worldwide, the company combines science, technology, and quality-driven processes to ensure safe and effective clinical products. Role Description We are seeking a skilled Automated Production Systems Technician to support the operation and optimization of advanced, automated manufacturing lines. The role involves ensuring production runs smoothly, adhering to GMP standards, and contributing to process improvements within a regulated environment. Responsibilities -Operate and oversee automated production equipment following SOPs and GMP requirements. -Troubleshoot issues and conduct root cause analysis to resolve technical problems. -Adjust mechanical and process parameters to maximize machine performance. -Record, verify, and manage production data in SAP/MES systems accurately. -Monitor process performance, identify deviations, and escalate when necessary. -Prepare accurate GMP documentation, including batch records and logs. -Participate in problem solving sessions with QA, Engineering, and Production teams. -Carry out equipment setup and shutdown procedures. Requirements -Minimum of 3 years’ experience in a similar production or manufacturing role, ideally in assembly and packaging. -Proven experience working with automated production…
SIRE® Life Sciences
SIRE® Life Sciences is the market-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.