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
Interim Senior L&D Programme Manager
The Company Our client is an international organisation operating across multiple markets, with a strong focus on developing its people, strengthening organisational capabilities and building a future-ready workforce. Learning, development and talent transformation are key priorities within its HR strategy. About the Role We are looking for an experienced Interim Senior L&D Programme Manager to lead several high-priority Learning & Development initiatives. In this strategic role, you will take primary ownership of the Digital Learning Ecosystem and contribute to the organisation-wide Skills Programme. You will also lead the implementation of SHL development assessments and coordinate selected High Performing Team interventions across EMEA. Working closely with Digital HR, internal L&D teams, HR stakeholders, business leaders and external partners, you will provide strategic direction, drive project delivery and ensure that learning initiatives align with wider organisational capability priorities Responsibilities – Lead the L&D roadmap and programme delivery for the Digital Learning Ecosystem. – Provide direction to internal teams and coordinate project planning and execution with Digital HR and external vendors. – Drive improvements in digital learning technologies, learner experience, accessibility and adoption.…
Food Safety and Quality Specialist
The Company: An international organization operating within food production and nutritional ingredients, supplying products to both business and consumer markets worldwide. The production environment has a strong focus on quality, food safety, compliance and continuous improvement. About the Role We are looking for a Food Safety and Quality Specialist for a full time assignment in Beilen. You will take ownership of the validation management system and act as the Quality Assurance representative within validation, technical and packaging projects. You will collaborate closely with Production, Engineering, Technology, Maintenance and R&D to ensure that processes meet applicable quality and food safety requirements. Responsibilities: – Set up, integrate, maintain and continuously improve the validation management system and associated documentation – Prepare, execute and periodically review the Site Validation Master Plan – Represent Quality Assurance in validation, technical and packaging projects – Translate and implement quality policies and quality documentation – Advise employees and management on quality, food safety and quality management systems – Support and verify CAPA and change management activities – Conduct internal audits and support external audits – Deliver training related…
Electronics UI Engineer
About the Company A global health technology company developing advanced medical systems and solutions to improve healthcare and patient outcomes worldwide. Role Description As an Electronics UI Engineer, you will contribute to the development and improvement of electronic hardware components and subsystems for advanced medical imaging systems. You will translate application and performance needs into technical requirements, evaluate supplier designs, conduct hands-on testing and solve engineering challenges in a multidisciplinary R&D environment. Key Responsibilities Provide technical expertise on non-graphical user interface hardware, components and configurations. Define technical requirements at subsystem and unit level, translating application performance needs into design improvements. Evaluate supplier prototypes and recommend technical design improvements. Perform feasibility studies and functional testing, including building test setups, gathering data and analysing results. Investigate and troubleshoot electronic subsystems and components. Assess component and subsystem performance, reliability, risks and safety. Collaborate with multidisciplinary teams, including Mechanical Engineering, Quality, Verification, Compliance, Lifecycle Management and Project Management. Take ownership of assigned units and contribute to wider engineering projects. Requirements At least 5 years of relevant engineering experience within the consumer or professional electronics…
Usability Engineer
About the Company An international organization operating in a highly regulated medical technology environment, focused on developing safe and reliable products for users worldwide. Role Description As a Usability Engineer, you will ensure that products are safe and intuitive to use throughout the design and development process. You will lead usability engineering and risk management activities, working closely with multidisciplinary teams to identify potential use-related risks, implement mitigations and demonstrate product safety in line with relevant regulatory requirements. Key Responsibilities Lead usability engineering activities throughout the product design and development lifecycle. Conduct workflow analysis, user research and task analysis to identify user needs and define usability requirements. Lead Usability FMEA and collaborate with Risk Management to identify, assess and mitigate potential risks. Develop usability engineering plans and coordinate activities with project teams and relevant stakeholders. Plan, conduct and document usability evaluations, ensuring critical findings are addressed. Analyse post-market data and identify potential usability-related issues. Advise design teams on usability aspects of product and design changes. Support the development of user-centred interfaces and safe-to-use products. Define and execute design validation strategies,…
QC Microbiology
Company Our client is a global pharmaceutical manufacturing organisation with a strong focus on quality, patient safety, and compliance. Their site operates in a highly regulated environment and is committed to continuous improvement, high standards of hygiene and safety, and reliable delivery of laboratory results that support product release. Job Description For our client, we are looking for a QC Microbiology Technician (Sterility & Endotoxin Testing) to perform routine and non-routine microbiological testing on a variety of samples in a regulated laboratory environment. The role is hands-on and includes testing, accurate documentation in digital systems, and supporting investigation and improvement activities to ensure quality standards and timelines are met. Responsibilities – Perform routine and non-routine microbiological analyses according to approved procedures and quality standards – Carry out bioburden testing using membrane filtration and plate-based methods – Test for specific microorganisms using selective/elective growth media – Perform endotoxin testing using gel-clot and kinetic chromogenic methods – Execute sterility testing on finished products – Support microorganism identification using methods such as Gram staining and/or MALDI-TOF – Perform growth media release testing…
Microbiology QC Analyst (GMP Laboratory)
Company Our client is a regulated, science-driven organisation operating in a GMP environment. The team supports product quality and patient safety through robust laboratory testing, strong documentation practices, and continuous improvement of quality processes. Job Description The Microbiology QC Analyst (GMP Laboratory) will perform routine and non-routine microbiological testing on a variety of samples in a controlled laboratory setting. The role combines hands-on analysis with accurate data recording in laboratory systems, while supporting deviations, investigations, and ongoing improvements to methods and documentation. Responsibilities – Perform routine and non-routine microbiological analyses according to approved procedures – Conduct key microbiology tests, including: Bioburden testing (e.g., membrane filtration, plate methods) Testing for specified microorganisms using selective/elective media Endotoxin testing (e.g., gel-clot and kinetic chromogenic techniques) Sterility testing on finished products Microorganism identification (e.g., Gram staining and/or MALDI-TOF) Media release testing – Work safely in controlled environments (e.g., safety cabinets/isolators) and follow aseptic practices – Record and report results accurately in laboratory systems (e.g., LIMS) – Maintain a clean, compliant work area; support equipment cleaning and basic upkeep – Identify, escalate, and help document…
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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