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.

Life Sciences Consultancy & Project Management

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Biotechnology

Senior Project Manager

📍 Breda, Noord-Brabant

⚙️ Ref: 59186

The Company Our client is one of the leads from the Biotechnology industry who try to improve patients’ lives, by distributing their medicines to hospital and pharmacies in 100 different countries in the world, to over 10 million patients, in Europe, Turkey, Middle East and Africa Regions. Job Description As a Senior Project Manager, you will lead complex manufacturing technology and digital innovation projects from planning and design through implementation, validation, and operational handover. You will coordinate cross-functional teams, vendors, and technology stakeholders to deliver automation, MES, IT/OT, digital manufacturing, and data-driven solutions within a regulated manufacturing environment. Key Responsibilities Lead construction and installation of manufacturing technology and digital projects from initial planning to operational launch. Define project scope, objectives, timelines, budgets, and resource needs. Develop detailed project plans, including milestones, dependencies, risks, and decision points. Manage project execution, monitor progress, and communicate with stakeholders to align expectations. Oversee the deployment of automation systems, data platforms, and digital manufacturing solutions. Coordinate requirements gathering, design reviews, testing, validation, and system qualification processes. Ensure technical solutions meet business needs and adhere to…

Biotechnology

Commercial Contracts & Pricing Coordinator

📍 Breda, Noord-Brabant

⚙️ Ref: 59191

Company: A global leader in biotechnology and pharmaceuticals, dedicated to discovering, developing, and delivering innovative medicines that improve patient outcomes worldwide. The organization operates with a strong commitment to scientific excellence, technological innovation, and patient-centric values. Their diverse and inclusive teams work across various regions to support health solutions in complex, regulated environments. Job Description: We are seeking a detail-oriented and proactive Commercial Contracts & Pricing Coordinator to join a dynamic, international team. In this role, you will support the operational execution and governance of contracts and pricing processes across multiple ex-US markets. The position plays a critical part in ensuring compliance, process efficiency, and accurate implementation of contractual terms within operational systems. Responsibilities: – Act as the main point of contact for external stakeholders and internal teams across approximately 112 countries, providing guidance on contracts and pricing activities. – Support governance and continuous improvements in contracts and pricing processes, policies, and systems. – Translate contractual agreements into operational system configurations, ensuring correct tax classifications and compliance with financial standards. – Collaborate with affiliates and global teams to implement contractual…

Pharmaceuticals

Senior Project Manager – Manufacturing Technology & Digital Innovation

📍 Breda, Noord-Brabant

⚙️ Ref: 59190

About our client   Our client is a global biopharmaceutical company with a major manufacturing site in Breda, the Netherlands. The site plays an important role in the production and supply of medicines and continues to invest in manufacturing capacity, technology, automation and digital innovation. As part of this ongoing development, the organization is working on projects that connect manufacturing, engineering, automation, IT/OT, digital systems and operational teams.   About the position We are looking for a Senior Project Manager to lead complex technology and digital manufacturing projects from initial concept through implementation and operational handover. You will work across Engineering, Manufacturing, Automation, IT/OT, Quality, Validation and external suppliers, making sure technology projects are delivered on time, within scope and in line with the requirements of a regulated manufacturing environment. The projects can cover areas such as manufacturing systems, automation, digital manufacturing, data solutions and technology infrastructure. This is a hands-on project leadership role for someone who is comfortable taking ownership, coordinating multiple stakeholders and driving projects from planning through to go-live.   Responsibilities Lead complex manufacturing technology and digital…

Pharmaceuticals

Quality Assurance Specialist

📍 Haarlem, Noord-Holland

⚙️ Ref: 59188

Company: A leading pharmaceutical manufacturing facility based in Haarlem, dedicated to distributing over 2,500 different medicines and vaccines to more than 140 countries. The organisation operates through integrated process teams and centres of excellence, ensuring high standards of quality and compliance across its global supply network. Job Description: We are looking for a detail-oriented Quality Assurance Specialist to join our client’s team. The role involves supporting the quality release process for pharmaceutical products, ensuring all batches meet rigorous quality standards, and maintaining compliance with regulatory requirements. The position offers an opportunity to work within a dynamic team in a fast-paced manufacturing environment. Responsibilities: -Review and support investigations into deviations, complaints, and corrective and preventive actions (CAPAs). -Contribute to fostering a strong culture of quality awareness within the Haarlem production site. -Act as the quality representative in various projects, especially during the introduction of new products. -Assist different departments with GMP practices and implementing change controls. -Review and approve GMP documentation such as SOPs, validation/qualification reports, and change control records. -Collaborate closely with the vaccination packaging team, quality control laboratories, and…

Food

Production Site Manager

📍 Noordwijk, Groningen

⚙️ Ref: 58870

Company Our client is a well-established food manufacturing organization supplying products to professional and consumer markets. The site operates in a dynamic, safety- and quality-driven environment, running a continuous production schedule and investing in operational improvement and technology upgrades. Job Description For a production site in Noordwijk, we are looking for an experienced Interim Production Site Manager (Food Manufacturing) to lead the factory through an important transformation phase. This role has full responsibility for day-to-day operations, performance improvement, and the further development of the site, with a strong focus on safety, food safety, quality, and operational excellence Responsibilities – Lead the site and ensure stable daily operations in a 24/7 production environment – Manage and develop the site leadership team across Production, Maintenance, – Technology/Operational Excellence, SHE, Quality, Planning & Logistics, and Finance – Drive improvements in safety performance, food safety standards, quality, and operational results – Strengthen processes, structure, and ways of working to improve performance and consistency – Lead change initiatives that build capability, ownership, and a continuous improvement culture on the shop floor – Support and guide technology upgrades…

Pharmaceuticals

Quality Assurance Specialist – Deviation Management

📍 Haarlem, Noord-Holland

⚙️ Ref: 59180

Company Our client is a leading organization in the pharmaceutical manufacturing industry, committed to maintaining the highest standards of quality in their production processes. They focus on ensuring product safety, compliance, and continuous improvement through innovative quality management practices. Job Description We are seeking a dedicated Senior Quality Assurance Specialist to join the team and support ongoing quality processes. The key focus of this role is to assist in reducing the current backlog of deviation investigations, with an emphasis on deviation handling and writing. The role involves working closely with production and the qualified person (QP) team to ensure compliance and quality standards are maintained, without participation in batch release activities. Responsibilities -Manage and resolve deviation reports, including investigating, writing, and documenting deviations. -Support the QA department in reducing deviation backlog and implementing quality improvements. -Review and approve master documents and specifications for product release. -Initiate and assess quality investigations, making informed decisions about product release or rejection. -Ensure timely completion of deviation reports (gDR/gLIR) and supervise corrective actions. -Oversee quality investigations to control risks in manufacturing processes. -Authorize and…

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Life Sciences Consultancy & Project Management Services

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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