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.
New Projects
Search for new Life Sciences Projects in the Netherlands
Response Planner
About the Company A global FMCG organization with a strong international presence and a highly integrated supply chain network. The company operates in a fast-paced environment focused on delivering excellent customer service, inventory performance, and operational efficiency across multiple markets. Role Description We are looking for a Response Planner to support the Benelux market during a temporary replacement assignment. In this role, you will be responsible for managing excess stock, monitoring service performance, mitigating supply risks, and coordinating with a wide range of stakeholders across the supply chain. This position requires a proactive and analytical professional who can quickly become operational and effectively manage changing priorities in a dynamic FMCG environment. Key Responsibilities Manage excess stock, blocked stock, residuals, and obsolescence activities. Identify supply chain risks and perform root cause analyses to drive corrective actions. Monitor inventory, service, and operational KPIs and communicate risks proactively. Coordinate with factories, planners, customer service teams, and business stakeholders. Support demand and supply reconciliation activities and mitigation planning. Own and maintain AATP business rules to optimize stock allocation and service levels. Drive local sell-off…
Drug Safety Case Study / Pharmacovigilance (Dutch Speaking)
Company Our client is a healthcare and life sciences organisation focused on patient safety, quality, and regulatory compliance. They work in a structured, international environment where accurate safety data and strong documentation are critical to protecting patients and meeting global regulatory expectations. Job Description We are looking for a Drug Safety Case Specialist to support the day-to-day pharmacovigilance activities related to adverse event intake, assessment, and reporting. The Drug Safety Case Specialist ensures safety information is processed accurately and on time, following internal procedures and applicable regulations, while working closely with cross-functional stakeholders to keep safety documentation complete and audit-ready. Responsibilities – Collect, review, and evaluate adverse event and safety information from internal and external sources – Triage incoming safety information and perform follow-up to obtain missing or unclear details – Process safety cases in line with internal procedures and regulatory requirements – Support timely and accurate safety reporting and documentation, as required – Perform data quality checks and ensure records are complete, consistent, and compliant – Maintain high-quality pharmacovigilance documentation and support audit/inspection readiness – Contribute to safety trend monitoring and…
Demand and Service Planning Specialist
Company: We are a supply-chain focused organization working to ensure products are available when customers need them. We support planning and operational execution through strong data, clear processes, and close collaboration with business stakeholders. Job Description: We are looking for a Demand and Service Planning Specialist to manage key availability and service performance drivers. The role focuses on short-term demand/supply reconciliation, effective use of allocation and availability rules, and proactive actions to protect customer service levels—while also addressing risks such as residuals, blocked stock, provisions, and obsoletes. Responsibilities: • Own accountability for residuals, blocked stock, provisions, and obsoletes to support effective service delivery. • Manage and continuously improve periodic AATP Business Rule review and adaptation to ensure accurate allocation decisions. • Deliver service in line with the operations strategy, including clear communication of service risks to the business. • Align escalation, allocation, and priority decisions for each customer in partnership with Sales and the Customer Service team. • Drive service performance against agreed service targets, ensuring corrective actions when needed. • Support short-term Demand/Supply reconciliation (
MSAT Process Development Specialist
The Company A global leader in healthcare innovation, dedicated to developing advanced therapies that improve patient outcomes worldwide. The company fosters a collaborative, science-driven environment focused on innovation, technology, and operational excellence. Role Description We are seeking an MSAT Process Development Specialist to join the Emerging Technologies team. In this role, you will support process development, technology deployment, and new product introduction projects while driving manufacturing efficiency, product quality, and continuous improvement across pharmaceutical operations. Responsibilities – Support process development, optimization, troubleshooting, and technology transfer activities. – Collaborate with R&D, Manufacturing, Quality, and cross-functional teams on innovation and improvement projects. – Assist with new product introductions, lifecycle management, and operational excellence initiatives. – Conduct data analysis, feasibility studies, and process improvement activities. – Ensure compliance with GMP requirements, validation standards, and regulatory guidelines. Requirements – Bachelor’s degree in chemistry, Pharmaceutics, Materials Science, Chemical Engineering, or a related scientific field. – 0–2 years of experience in pharmaceutical, biotech, chemical, or related industries. – Knowledge of process development, analytical techniques, and material characterization. – Understanding of cGMP, QbD, PAT, and validation principles.…
Associate Scientist – MSAT Pharmaceutical Process Development
Company We are a global healthcare organisation focused on innovation in manufacturing science and technology. In this role, you’ll support cross-functional teams to develop and deliver technology and science projects that strengthen product performance, reliability, compliance, and efficiency across the end-to-end product life cycle. Role Description Support MSAT and Emerging Technologies projects focused on pharmaceutical manufacturing, new product introductions, process improvements, technology transfer, and advanced manufacturing initiatives. Work with cross-functional teams to improve product quality, manufacturing efficiency, compliance, and cost performance. Key Responsibilities – Support new product introductions (NPI) and technology transfer activities. – Provide technical support for formulations, manufacturing processes, and analytical methods. – Assist with process development, process characterization, and manufacturing improvements. – Support quality, compliance, and cost reduction (COGS) initiatives. – Conduct feasibility studies, troubleshooting, and data analysis. – Collaborate with MSAT, Manufacturing, R&D, and external manufacturing sites. Requirements – Education – BS in Chemistry, Pharmaceutics, Chemical Engineering, Pharmaceutical Sciences, Materials Science, or related field. – Experience: 1–2 years of experience in pharmaceutical, biotech, MSAT, process development, analytical development, or formulation development. – Technical Skills Material characterization…
Quality Engineering Engineer (Level 3)
Company A leading engineering-focused organisation operating in the Netherlands. We support teams that value quality, collaboration, and continuous improvement in product and service delivery. Job Description Job Title: Quality Engineering Engineer (Level 3) We are looking for an experienced Quality Engineering Engineer (Level 3) to strengthen our engineering quality efforts in a hybrid working environment from Leiden, Netherlands. This role focuses on quality engineering practices and ensuring products and processes meet the expected standards. Responsibilities -Own and support quality engineering activities across relevant engineering workstreams -Collaborate with engineers and stakeholders to identify quality risks and improvement opportunities -Help define, maintain, and apply quality processes and standards to support reliable delivery -Conduct and support quality checks to ensure outcomes meet agreed requirements -Work as an effective member of a hybrid team, coordinating activities with colleagues onsite and remotely Requirements -Proven experience in quality engineering (Level 3 experience required) -Strong collaboration skills and ability to work closely with engineering teams -Knowledge of quality engineering principles and practices -Netherlands (NL) language proficiency required -No freelancers Other Information The supplier will need to provide a laptop for…
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.