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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Senior Specialist
The Company A global life sciences organization committed to improving health outcomes through a broad portfolio of healthcare products. Operating in a highly regulated environment, the company focuses on strengthening its global supply chain, managing supplier risks, ensuring regulatory compliance, and driving operational excellence. About the Role We are looking for an experienced Senior Specialist, Supplier Resiliency & Policy Compliance to lead and strengthen the organization’s Third Party Resilience program. In this role, you will be responsible for identifying, assessing, monitoring, and mitigating supplier-related risks across the global supply chain. You will work closely with Procurement, Supply Chain, Risk Management, and Internal Audit teams to ensure suppliers remain resilient, procurement policies are followed, and potential supply chain disruptions are identified and addressed proactively. Key Responsibilities Lead and enhance the Third Party Resilience program, ensuring supplier risks are identified, assessed, monitored, and mitigated. Develop and maintain supplier risk assessment methodologies, scoring models, and scorecards, including product risk assessments and mitigation plans. Drive N-Tier supplier mapping to improve supply chain visibility and identify potential supplier disruptions. Manage Procurement Policy Compliance and Internal…
Process Engineer
The Company A global pharmaceutical manufacturing organization focused on delivering high quality healthcare products within a highly regulated GMP environment. The company invests heavily in engineering excellence, validation, compliance, and continuous improvement to support complex manufacturing operations and ensure product quality and patient safety. About the Role The Commissioning Qualification Validation Engineer will support engineering and validation projects within a GMP manufacturing environment. This role focuses on developing and executing commissioning, qualification, and validation strategies for secondary packaging systems and computerized systems. The successful candidate will work independently while collaborating with project teams to ensure technical solutions comply with validation requirements, internal procedures, and regulatory standards. Responsibilities Develop and update validation documentation Lead commissioning, qualification, and validation activities for manufacturing systems. Support validation lifecycle activities from design through implementation and qualification. Provide technical validation guidance to project teams. Ensure project deliverables comply with GMP requirements and internal procedures. Drive execution of validation strategies for secondary packaging equipment and computerized systems. Coordinate testing activities and review validation outcomes. Support additional projects and tasks assigned by management. Requirements Experience with Assembly and…
Supply Network Planner
Company Our client is a well-established, international FMCG manufacturing organisation with a complex supply network. The environment is fast-moving and highly collaborative, with strong focus on customer service, inventory optimisation, product freshness, and continuous improvement across end-to-end supply chain operations. Job Description We are looking for a Short-Term Supply Network Planner to manage finished goods availability for a defined portfolio across multiple markets and supply locations. This role is central to creating feasible plans, resolving supply/demand exceptions, and coordinating with key stakeholders to protect service levels while balancing cost, inventory, and freshness requirements. Responsibilities – Maintain accurate short-term production plans and communicate updates to factory scheduling teams in a timely way – Own short-term finished goods availability across the assigned portfolio (including semi-finished products where relevant) – Manage product deployments within the assigned supply network based on market needs and stock availability – Identify and resolve exceptions in the 0–12 week horizon (demand vs. supply imbalances), including root cause analysis and corrective/preventive actions – Escalate capacity and material supply risks through the relevant planning governance – Run scenario planning and…
Project Manager (BioPharma Engineering)
Company The client is an innovative biopharmaceutical manufacturing organisation working in a highly regulated environment. They deliver critical therapies and operate to strict safety, quality and compliance standards. The site is fast-paced and project-driven, with ongoing investments in equipment, facilities and utilities to support manufacturing operations. Job Description For this Project Manager (BioPharma Engineering) (Capital Projects) position, we are looking for an organised, proactive professional to lead small to medium-sized engineering investment projects on a manufacturing site in the Netherlands. The Project Manager (BioPharma Engineering) (Capital Projects) will manage projects from early definition and feasibility through design, construction and final handover, ensuring delivery meets safety, quality, cost and schedule expectations. Responsibilities – Lead engineering capital projects across equipment, facilities and utilities from definition through handover – Run feasibility studies and translate needs into clear technical scopes and project proposals – Create and execute project plans, coordinating multidisciplinary teams and external partners – Supervise construction and technical execution activities, keeping delivery on track – Align with stakeholders across engineering, operations and project sponsors to support business case development and approvals –…
Microbiology Technician
Company Our client is a well-established organisation in the life sciences sector, working on research and development projects that support the creation, testing, and improvement of biological products. The environment is hands-on and collaborative, with strong focus on quality, accurate record-keeping, and working safely and consistently in the laboratory. Job Description We are looking for a Microbiology Technician to support a busy research laboratory in Boxmeer. The Laboratory Research Technician will work across different projects and activities, helping the team deliver reliable laboratory results and maintain accurate documentation. The work is fully on-site and requires flexibility, as the daily tasks can vary based on project needs. Responsibilities – Support laboratory research activities across multiple projects and teams – Perform sample processing and general laboratory tasks as required – Carry out testing activities such as immunoassays (e.g., ELISA/AlphaLISA) and other laboratory experiments – Support bacteriological and virological testing activities, depending on project requirements – Contribute to stability and potency testing activities for biological products – Assist with laboratory work connected to animal studies when needed – Record work accurately and maintain complete…
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.
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