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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Automated Production Technician
About the Company: Our client is a leading pharmaceutical manufacturing company that produces high-quality medicines in a clean, modern, and highly regulated production environment. Safety, quality, teamwork, and continuous improvement are key priorities across the organisation. About the Role: We are looking for an Automated Production Technician to join a GMP-regulated manufacturing team. In this role, you will operate and monitor automated production equipment, help resolve technical issues, complete production documentation, and ensure products are manufactured safely and according to quality standards. You will work closely with colleagues from Production, Quality, Engineering, and Maintenance to keep the production process running smoothly and efficiently. Key Responsibilities: -Operate and monitor automated production equipment in accordance with GMP guidelines and standard operating procedures (SOPs). -Identify, troubleshoot, and report equipment or production issues. -Perform basic machine adjustments to support efficient production and minimise downtime. -Accurately record production data and activities in SAP and MES systems. -Monitor the manufacturing process and escalate deviations or quality concerns when required. -Complete production documentation, including batch records and production logs. -Support line setup, product changeovers, and shutdown activities.…
Supply Chain Lead
Company We are representing a leading organization committed to excellence in logistics and supply chain management within the pharmaceutical and healthcare sectors. The company prioritizes quality, compliance, and continuous improvement, operating with integrity and a focus on innovative cold chain solutions. Job Description We are seeking a dedicated Supply Chain & Cold Chain Operations Manager to oversee the end-to-end management of regional distribution, ensuring service levels are met within budget while maintaining strict compliance with GDP standards. The role involves developing and optimizing cold chain logistics, building strong partner relationships, and supporting continuous process improvement initiatives. Responsibilities -Manage supply chain operations to ensure customer service levels are achieved efficiently and within budget, adhering to GDP standards. -Develop, select, and implement cold chain solutions as part of the Supply chain network. -Conduct regular performance reviews with supply chain partners, handle escalations, and foster continuous improvement initiatives. -Support internal stakeholders by maintaining excellent relationships and escalating issues when needed. -Oversee agreements and contracts with supply chain providers. -Drive continuous improvement initiatives to identify cost savings and efficiency opportunities, while -enhancing quality,…
Regulatory Affairs Specialist
About the Company Our client is an international organization within the food industry, operating across multiple markets and product categories. Within a global Quality and Regulatory environment, the organization focuses on ensuring product compliance while supporting innovation and business growth. Role Description As a Regulatory Affairs Specialist, you will ensure compliance with food legislation and customer requirements across an international product portfolio. You will monitor regulatory developments, assess their business impact and advise stakeholders on practical solutions. Working closely with Quality, R&D, Supply Chain, Sales and Marketing, you will support product development, labeling, market introductions and regulatory projects. Key Responsibilities Monitor food legislation and regulatory developments and assess their impact. Review and approve labels, packaging, claims and communication materials. Provide regulatory guidance throughout product development and innovation projects. Conduct regulatory risk assessments and impact analyses. Advise stakeholders on food legislation and compliance requirements. Support the resolution of compliance issues and non-conformities. Contribute to regulatory policies, guidelines and process improvements. Support customer and market-related regulatory questions. Collaborate with international Regulatory Affairs and Quality teams. Develop expertise in areas such as packaging,…
Automated Line Operator
The Company A leading pharmaceutical manufacturing organization with a strong focus on automation, quality, GMP compliance, and operational excellence. The company operates advanced production facilities where technology and continuous improvement are key to maintaining reliable manufacturing processes. Role description As an Automated Line Operator, you will play an important role in keeping automated production and packaging operations running safely and efficiently. You will operate and monitor equipment, troubleshoot technical issues, maintain GMP standards, and support improvements across the production process. You will work closely with Production, Maintenance, Quality, and Engineering teams to maintain smooth operations and quickly respond to production challenges. Responsibilities Operate and monitor automated production and packaging equipment Perform equipment setup, changeovers, and shutdown activities Monitor machine performance and production output Troubleshoot technical and process-related issues Adjust machine settings and parameters to maintain optimal performance Record production activities and data in SAP and MES Complete accurate GMP documentation and production records Identify and escalate deviations or abnormalities when required Support root cause analysis and structured problem-solving activities Work with Production, Quality, Maintenance, and Engineering teams to…
Food Regulatory Affairs Expert
Company: A leading organization dedicated to food innovation and safety, committed to ensuring compliance with international food regulations while supporting product development and business growth. The company values scientific expertise, collaboration, and continuous improvement to deliver high-quality products to consumers worldwide. Job Description: We are seeking a knowledgeable Food Regulatory Affairs Expert to join our client’s team. This key role involves ensuring that products and business processes adhere to food legislation and internal policies across a global portfolio. The successful candidate will translate complex regulations into practical solutions, support innovation, and act as a trusted advisor across various departments. Responsibilities: – Monitor changes in food legislation, regulations, and industry standards; evaluate their impact on products and processes. – Review and approve product labels, packaging, claims, and communication materials to ensure compliance. – Provide regulatory guidance throughout the product development cycle, from concept to launch. – Conduct risk assessments for new ingredients, packaging changes, and legislative updates. – Advise colleagues in Sales, Marketing, Supply Chain, R&D, and Manufacturing on regulatory requirements. – Assist in resolving compliance issues by identifying risks and…
Regulatory Affairs Specialist
Company A leading organization dedicated to delivering high-quality food products, committed to compliance, innovation, and sustainability. The company operates within a complex, international environment, collaborating across various functions to ensure products meet all regulatory standards and customer expectations. Role Description We are seeking a Regulatory Affairs Specialist to join our client’s dynamic team. In this role, you will ensure that all products and processes comply with food legislation, internal policies, and customer requirements on a global scale. You will work closely with teams across R&D, Quality, Supply Chain, Sales, and Marketing to facilitate innovation while maintaining compliance. Responsibilities – Monitor global food legislation, regulations, and industry standards, evaluating their impact on the business. – Review and approve product labels, packaging, claims, and communication materials to ensure regulatory compliance. – Provide regulatory guidance during product development and innovation projects, from initial concept to launch. – Conduct risk assessments and impact analyses for new products, ingredients, packaging changes, and legislative updates. – Advise internal teams on regulatory requirements and support resolution of compliance issues by identifying risks and developing practical solutions. –…
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.