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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Quality Assurance Specialist
The Company A leading pharmaceutical manufacturing organization focused on producing high quality medicines in a highly regulated environment. The company emphasizes quality, compliance, continuous improvement, and operational excellence across its production activities. About the Role This role is responsible for supporting and maintaining quality assurance activities within pharmaceutical manufacturing operations. The position focuses on ensuring GMP compliance, investigating deviations, driving CAPA initiatives, and supporting continuous improvement efforts. The successful candidate will work closely with production teams to enhance quality systems and maintain regulatory standards. Responsibilities -Write and manage production deviations and quality events -Monitor manufacturing processes and identify deviations from established procedures -Investigate quality issues, complaints, and non-conformances -Perform root cause analysis and develop CAPA plans -Support compliance investigations and quality improvement initiatives -Review SOPs, validation protocols, production documentation, and batch manufacturing records -Ensure compliance with GMP and company quality standards -Recommend improvements related to product quality, safety, health, and environmental standards -Participate in cross-functional quality and compliance projects -Provide quality related guidance and support to manufacturing teams -Maintain accurate documentation and reporting of quality activities Requirements -Master’s degree or…
Validated Systems Engineer
Company Our client is a global, innovation-driven organisation operating in a highly regulated manufacturing environment. The site focuses on reliable delivery of critical products and works to high quality and compliance standards. Teams collaborate closely across Manufacturing, Quality, Engineering and Technology to improve processes and keep operations running smoothly. Job Description We are looking for a Validated Systems Engineer to strengthen the Operations Technology team in Breda. This position sits at the intersection of digital technology and the production floor, helping to improve reliability, efficiency and compliance of packaging and labelling operations. The Validated Systems Engineer will support and improve a defined set of manufacturing systems (including SCADA and system integrations), working with site stakeholders and global teams to deliver practical solutions in a GMP-regulated environment. Responsibilities – Support the design, testing, qualification and change-control of manufacturing systems in line with GMP requirements and site procedures. – Maintain and troubleshoot a portfolio of operational manufacturing systems to ensure stable day-to-day performance. – Work with cross-functional stakeholders (Manufacturing, Quality, Engineering and Technology) to identify issues, root causes and improvement opportunities. –…
Manufacturing Systems Support Engineer
Company: We are working with a leading global biopharmaceutical company dedicated to developing and manufacturing innovative medicines. Their Breda site focuses on delivering high-quality products through advanced manufacturing and technology solutions, with a strong emphasis on compliance, reliability, and continuous improvement. Job Description: The Manufacturing Systems Support Engineer plays a vital role in ensuring the reliability, efficiency, and compliance of labelling and packaging operations. This position involves working at the intersection of digital technology and manufacturing, supporting critical systems such as SCADA, automated label printing, and mobile workstations. It is an active, hands-on role suited for someone who enjoys technical problem-solving and seeing the direct impact of their work on manufacturing continuity. Responsibilities: • Assist in the design, testing, qualification, and change management of manufacturing systems in accordance with GMP guidelines. • Collaborate with internal teams across Breda and globally, as well as external technology partners, to identify improvement opportunities. • Maintain, troubleshoot, and support a portfolio of manufacturing systems supporting both commercial and clinical production. • Document processes and train staff on new technologies and systems. • Identify recurring…
Senior Quality Investigator
The Company A leading global pharmaceutical manufacturing organization focused on producing high quality medicines within a highly regulated GMP environment. The business operates large scale production facilities and places strong emphasis on quality, compliance, continuous improvement, and patient safety. The organization is currently strengthening its quality investigation capabilities to support production operations and ensure timely closure of quality events and deviations. Role description This role focuses on managing pharmaceutical quality investigations and supporting production teams with deviation management activities. The successful candidate will work closely with manufacturing teams to investigate production related deviations, perform root cause analysis, drive CAPAs, and ensure investigations are completed according to GMP requirements. This is an excellent opportunity for someone with hands on pharmaceutical quality experience who can quickly contribute within a fast paced production environment and independently drive investigations to closure. Responsibilities – Write, review, and manage deviation records – Conduct quality investigations within GMP environments – Perform root cause analysis for production related deviations – Develop and document CAPAs – Drive investigations toward timely closure – Support production teams with quality and compliance…
Maintenance Technician (Shift Based)
Company Our client is an established production organisation in the food industry, operating in a safety- and quality-driven environment. The site works with modern technical installations and relies on a strong maintenance team to keep operations running smoothly and reliably. Job Description We are looking for a Maintenance Technician (Mechanical & Electrical) to support daily production by resolving breakdowns quickly and performing preventive maintenance. The Maintenance Technician (Mechanical & Electrical) ensures equipment and facilities remain in good technical condition, with a strong focus on safe working and minimal downtime. Responsibilities – Diagnose and repair mechanical and electrical faults in installations inside and outside production areas. – Assess the type and impact of malfunctions and determine whether immediate repair is required. – Carry out preventive and corrective maintenance to keep equipment in good technical condition. – Supervise and coordinate external engineers/contractors when needed. – Identify and report important technical issues to the Chief Engineer. – Provide instructions to colleagues and keep them informed about technical matters. – Use hand tools and machine tools to process materials when required. – Work in…
Plant Manager Hay19|GLB_0969
The Company A reputable food manufacturing organization focused on producing high-quality food products in a safe, efficient, and well-organized production environment. The organization places strong emphasis on safety, quality, hygiene, technology, and continuous improvement.. About the Role The Production Supervisor will be responsible for managing a team and ensuring smooth and efficient production operations within one or more departments. The role focuses on safety, quality, production output, technical priorities, team development, and effective communication between shifts. Responsibilities Manage and coach a team of employees, providing clear direction and leading by example. Take operational responsibility for safety, quality, quantity, hygiene, and technology within one or more departments. Ensure production planning and targets are achieved while setting priorities for technical work. Analyse production complaints and identify causes to support effective corrective actions and improvements. Ensure effective shift handovers, contribute to work instructions, and maintain continuity between shifts. Requirements Proven experience managing and leading teams within a production or manufacturing environment. Strong understanding of production operations, with responsibility for safety, quality, hygiene, and output. Experience working with production planning and prioritising technical or…
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.