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
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Temporary Absence Management Case Manager
The Company The client is one of the Netherlands’ biggest dairy products manufacturers who is also active globally. Role Description We are seeking an experienced Absence Management Case Manager to support employees throughout their sickness absence and return-to-work journey. Acting as the central point of contact for employees, managers, and plant managers, you will oversee absence cases from the first day of absence in accordance with the Dutch Gatekeeper Improvement Act (Wet Verbetering Poortwachter). You will work closely with occupational health professionals, translate medical advice into practical action plans, and provide guidance throughout the reintegration process. As part of the Case Management team, you will support both office-based and operational employees across multiple locations, ensuring a compliant, employee-focused, and effective approach to absence management. In addition to day-to-day case management, you will contribute to continuous improvement initiatives and provide expert advice on absence prevention and wellbeing-related topics. Responsibilities Manage employee sickness absence cases from day one through to successful reintegration. Ensure compliance with the Dutch Gatekeeper Improvement Act (Wet Verbetering Poortwachter) and related legislation. Serve as the primary contact for…
Case Manager
The Company A leading international food production organization with operations across multiple locations and a strong focus on employee wellbeing, sustainable growth, and operational excellence. The company supports both manufacturing and office environments and offers a collaborative, people focused culture. About the Role As a Casemanager Verzuim, you will guide employees throughout their sickness absence and reintegration journey in accordance with Dutch legislation. You will act as the central point of contact for employees, managers, and site leaders, ensuring a smooth and compliant absence management process. This role combines operational case management with advisory responsibilities and continuous improvement initiatives aimed at reducing absenteeism and improving employee wellbeing. Responsibilities Manage employee sickness absence cases from the first day of absence Ensure compliance with the Wet Verbetering Poortwachter Conduct regular absence and reintegration meetings Translate occupational physician recommendations into actionable plans Advise employees, managers, and plant managers on absence related matters Support employees throughout reintegration processes Manage IVA and WIA application processes Contribute to absenteeism prevention strategies Participate in process improvement projects Travel regularly to multiple locations across Eastern Netherlands Requirements HBO…
Quality & Compliance Specialist
Company Our client is a leading organisation in the pharmaceutical manufacturing sector. They operate in a highly regulated environment and are committed to delivering safe, high-quality products through strong quality standards, continuous improvement, and a culture where compliance and collaboration are key. Job Description We are looking for a Quality & Compliance Specialist to support day-to-day production by ensuring activities are performed in line with GMP requirements and internal quality standards. The role focuses on deviation support, investigations, CAPA follow-up, and strengthening documentation practices across manufacturing and packaging operations. Responsibilities – Support manufacturing and packaging teams with deviations and quality-related questions. – Assess deviations and advise whether production activities should be paused or stopped when needed. – Monitor production processes and identify deviations from established procedures. – Investigate and document deviations and complaints, ensuring clear, compliant records. – Perform and document root cause investigations and drive CAPA actions to closure. – Propose and support improvements to production methods, processes, and product quality. – Contribute to continuous improvement initiatives, including actions from internal/external audits. – Review and support updates to SOPs,…
Customer Collaboration Specialist
The company A leading international consumer goods organisation with a global presence and a strong focus on sustainable growth, operational excellence, customer satisfaction, and continuous improvement. The organisation brings together commercial, supply chain, and operations teams to deliver excellent customer service and efficient end-to-end execution. Role Description As a Customer Collaboration Specialist, you play a pivotal operational role within the supply chain, connecting customers with internal teams across logistics, planning, sales, marketing, finance, and order management. You will act as a key point of contact for customers regarding customer service, logistics, order fulfilment, and operational supply chain topics. Through customer analytics and proactive collaboration, you will identify service and cost improvement opportunities, resolve operational issues, and drive continuous improvement across the order-to-cash process. Responsibilities – Act as the primary operational contact for customers regarding customer service and logistics-related topics. – Analyse customer operations, performance data, and supply chain processes to identify improvement opportunities. – Monitor customer KPIs and identify opportunities to improve service, cost, speed, and delivery performance. – Initiate, coordinate, and lead improvement projects within customer operations and order…
Facility Engineering Lead
The Company A global pharmaceutical manufacturing organization focused on delivering high quality medicines through advanced engineering, manufacturing, and packaging operations. The company operates large scale GMP regulated facilities and invests heavily in facility modernization, compliance, and operational excellence. Role description The Facility Engineering Lead will be responsible for leading the facility engineering scope of a major high potency secondary packaging expansion project. The role focuses on facility design, construction, commissioning, qualification, and operational readiness within a GMP regulated pharmaceutical environment. Working closely with engineering teams, contractors, operations, quality, and EHS stakeholders, the successful candidate will ensure facility systems are delivered safely, compliantly, and on schedule. Responsibilities – Lead facility engineering activities across design, procurement, construction, commissioning, qualification, and turnover phases – Support development and review of facility concepts, Basis of Design documentation, and detailed engineering packages – Review and approve technical specifications, calculations, vendor documentation, and engineering deliverables – Coordinate Civil Structural Architectural activities – Manage HVAC, Black Utilities, fire protection, and building infrastructure engineering scope – Ensure compliance with GMP requirements, engineering standards, local regulations, and EHS expectations –…
Facility Engineering Lead
About the Company Our client is a global pharmaceutical organization developing and manufacturing medicines in a GMP environment. The Haarlem site is expanding its facilities to support high-potency secondary packaging operations. Role Description As Facility Engineering Lead, you will lead the facility engineering scope for a major GMP facility project. You will coordinate Civil, Structural & Architectural (CSA), HVAC, utilities, fire protection, and related building systems from design through construction, commissioning, and qualification. Key Responsibilities Lead facility engineering activities across the project lifecycle Review designs, calculations, specifications, and vendor documentation Coordinate CSA, HVAC, utilities, fire protection, and building systems Ensure compliance with Dutch regulations, GMP, EHS, and engineering standards Coordinate interfaces with process equipment, automation, utilities, and site operations Support design reviews, risk assessments, constructability reviews, and GMP reviews Support commissioning, qualification, turnover, and operational readiness Coordinate with contractors, engineering partners, Quality, EHS, Operations, and Procurement Own assigned facility workstreams and resolve technical issues Requirements Strong experience in facility engineering within pharmaceutical or GMP environments Proven experience with large-scale engineering or construction projects Strong knowledge of HVAC, utilities, building systems,…
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.