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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Pharmaceuticals

Pharmaceutical Manufacturing Associate

📍 Breda, Noord-Brabant

⚙️ Ref: 59002

About the Company A global leader in pharmaceutical manufacturing, committed to delivering high-quality healthcare products that improve patients’ lives worldwide. The company operates within a highly regulated environment and is dedicated to maintaining the highest standards of quality, compliance, safety, and operational excellence. Role Description We are seeking a motivated and detail-oriented Pharmaceutical Manufacturing Associate to join a dynamic production team. In this role, you will be responsible for supporting manufacturing operations in a GMP-regulated environment, ensuring all production activities are carried out in accordance with approved procedures, quality standards, and safety requirements. Responsibilities – Execute manufacturing activities in accordance with Standard Operating Procedures (SOPs) and GMP regulations. – Perform manual production and operational tasks to support manufacturing processes. – Conduct in-process quality checks to ensure product quality and compliance. – Accurately complete batch records, logbooks, and production documentation. – Identify, report, and support the investigation of deviations and quality issues. – Assist with equipment preparation, setup, cleaning, and maintenance activities. – Support production changeovers and operational readiness activities. – Ensure the manufacturing area remains clean, organized, and audit-ready. – Follow…

Pharmaceuticals

Maintenance Engineer

📍 Leiden, Zuid-Holland

⚙️ Ref: 59245

Over het bedrijf Een internationale farmaceutische organisatie die innovatieve geneesmiddelen ontwikkelt binnen een sterk gereguleerde GMP-productieomgeving. Functieomschrijving Als Maintenance Engineer ondersteun je de Business System Owner bij het beheer van farmaceutische watersystemen, waaronder WFI/WDI, BMS en EMS. Je zorgt voor de betrouwbaarheid van installaties, GMP-compliance en operationele gereedheid en draagt bij aan onderhoudsstrategieën, investeringsplannen en technische projecten. Belangrijkste verantwoordelijkheden Beheren van clean utility-assets om betrouwbaarheid, beschikbaarheid, kwaliteit en kostenefficiëntie te waarborgen Ondersteunen van langetermijnonderhoudsstrategieën en CAPEX-investeringsplannen Beoordelen en beheren van wijzigingen (MoC) tijdens ontwerp, commissioning en kwalificatie Beoordelen van technische gegevens en de impact van voorgestelde wijzigingen Ondersteunen van engineeringprojecten en zorgen voor een goede overdracht en operationele gereedheid Bewaken van naleving van GMP-, EHS- en interne assetmanagementvereisten Identificeren en implementeren van verbeteringen aan clean utility-systemen Samenwerken met de Business System Owner en de Maintenance- en Engineeringteams Vereisten Minimaal 2 jaar ervaring binnen een farmaceutische/GMP-omgeving Praktische ervaring met WFI/WDI-clean utility-systemen — must-have Ervaring met assetmanagement en onderhoud van farmaceutische utilities Kennis van BMS en besturingssystemen voor clean utilities Kunnen lezen en aanpassen van P&ID’s Kennis van GMP, Management of Change,…

Pharmaceuticals

Senior Utility Systems Technician

📍 Breda, Noord-Brabant

⚙️ Ref: 59256

Company A leading pharmaceutical manufacturing facility committed to delivering life-changing medicines worldwide. The organization operates a modern and highly automated site, employing a diverse team dedicated to maintaining safety, quality, and efficiency across all operations. Job Description We are seeking a skilled and proactive Senior Utility Systems Technician to oversee and maintain critical utility systems that support manufacturing, warehousing, and office functions. The role combines technical expertise, leadership, and a focus on continuous improvement to ensure the reliable operation of essential infrastructure. Responsibilities – Coordinate and prioritize maintenance activities for utility systems and facility infrastructure. – Provide technical guidance, coaching, and support to technicians, contractors, and team members. – Assist in troubleshooting complex issues related to utilities and building systems. – Collaborate with facilities, engineering colleagues, vendors, and contractors to resolve technical challenges. – Drive initiatives to improve system reliability and operational efficiency. – Participate in an on-call rotation to support critical utility systems outside regular working hours. Requirements – Technical education at MBO+/HBO level or equivalent experience. – Experience in utilities, facilities maintenance, or industrial settings. – Strong troubleshooting…

Pharmaceuticals

Clinical Supply Chain QA Specialist

📍 Breda, Noord-Brabant

⚙️ Ref: 59254

Company Our client is a globally operating organization in the life sciences sector, focused on delivering high-quality medicines for patients worldwide. The site in the Netherlands plays a key role in labelling, packaging, storage, and distribution for both commercial and clinical supply chains, working in a fast-paced, international environment with high quality and compliance standards. Job Description For our client in Breda, we are looking for a Clinical Supply Chain Quality Assurance Specialist to provide QA oversight across the clinical supply chain and support production-related quality activities. The role ensures investigational medicinal products are handled in full compliance with GMP/GDP requirements, supporting smooth release, distribution, and packaging/labelling operations for clinical trials. Responsibilities – Provide quality guidance and oversight for investigational medicinal products to ensure GMP/GDP compliance – Review batch documentation to support batch certification activities – Review and approve clinical label artwork and support packaging/labelling quality checks – Assess and document temperature excursions during transport and at clinical sites/depots – Support investigation and resolution of quality/compliance issues related to manufacturing, packaging, and distribution – Review and approve minor deviations in…

Pharmaceuticals

Manufacturing Process Technician

📍 Breda, Noord-Brabant

⚙️ Ref: 59253

Company A global manufacturing organization operating within a GMP-regulated environment, focused on delivering quality products that improve patients’ lives. The company values innovation, teamwork, operational efficiency, and a strong culture of compliance and continuous improvement. Role Description As you are responsible for operating high-tech manufacturing equipment in a GMP-regulated environment, ensuring production runs smoothly, efficiently, and in full compliance with strict quality standards. As a Manufacturing Process Technician, you play a critical role in supporting the timely delivery of high-quality medicines, contributing directly to the organization’s commitment to patients and operational excellence. Responsibilities – Operate and monitor automated production and packaging equipment in line with GMP and SOP requirements. – Perform troubleshooting and root cause analysis (RCA) to resolve equipment and process issues. – Optimize machine settings and process parameters to improve efficiency and performance. – Maintain accurate GMP documentation, batch records, and production logs. – Record and verify production data using SAP, MES, or ERP systems. – Participate in cross-functional problem-solving and triage meetings with QA, Maintenance, and Production teams. – Carry out equipment setup, changeovers, line clearance, and…

Food

GMP Operator

📍 Breda, Noord-Brabant

⚙️ Ref: 59252

Company Our client is an international manufacturing company operating in a highly regulated production environment. The organisation uses advanced automated manufacturing and packaging technologies to deliver high-quality products while maintaining strong standards for safety, compliance, and operational excellence. The site values teamwork, continuous improvement, technical expertise, and innovation. Job Description We are looking for a Manufacturing Operator to join a dynamic production team. In this role, you will help keep semi-automated production and packaging lines running safely, efficiently, and according to GMP requirements. You will monitor equipment, handle basic technical issues, complete production activities, and support the team in keeping production running smoothly. Roles & Responsibilities – Run and monitor semi-automated production and packaging lines in a GMP environment. – Set up and start production equipment according to SOPs and production instructions. – Check and adjust machines and process settings when needed. – Carry out cleaning, product changeovers, line clearance, and basic equipment checks. – Identify and troubleshoot machine or process issues to reduce production downtime. – Make basic machine adjustments to keep the production process running smoothly. – Record 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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