Life Sciences Consultancy & Project Management in Netherlands

The Company A leading global biotechnology organization with a strong focus on innovative manufacturing, advanced automation, quality, and operational excellence. The organization operates in a highly regulated GMP environment and invests in reliable, secure, and sustainable manufacturing technologies. Role Description As a Senior Automation Engineer, you are responsible for the automation aspects of new and upgraded manufacturing equipment across Device Assembly, Inspection, Labeling, and Packaging. You will oversee automation throughout the equipment lifecycle, from design and installation through commissioning, qualification, and operational support, while ensuring reliability, compliance, security, and continuous improvement. Responsibilities – Lead and manage automation activities according to project timelines and requirements. -Support New Product Introduction (NPI) activities and equipment implementation. – Author and review automation design documents, including URS, FDS, HDS, and SDS. – Support FAT, commissioning, testing, and qualification activities at vendors and on-site. – Implement automation hardware, software, and security standards. – Ensure equipment complies with required cybersecurity and monitoring standards. – Participate in Data Integrity Assessments and Automation Preventive Maintenance activities. – Develop backup/restore procedures, work instructions, parameter lists, and audit trail review procedures.…

Duration: 6 months Location Hoofddorp    About our client Our client is a leading biopharmaceutical company focused on developing innovative treatments for cancer. The organisation operates a GMP-regulated manufacturing site in the Netherlands and works within a highly regulated quality environment. You will join a Quality Systems team that works across the site and collaborates with multiple departments to maintain and continuously improve the quality management system. About the position We are looking for a Senior Specialist I – Quality Systems for a 6-month assignment. In this role, you will support the management and continuous improvement of key Quality Systems, with a strong focus on Change Control, Deviations, CAPA, Material Review and quality metrics. You will work closely with different departments across the site, provide training on Quality Systems and support quality governance and compliance activities. Responsibilities Manage and maintain Change Control, Deviation and CAPA systems Support and act as backup chair for relevant quality review boards Manage the Material Review Board process Deliver and coordinate Quality Systems training Monitor site compliance with quality procedures and requirements Review and approve…

About our client Our client is a global biotechnology company developing and manufacturing innovative medicines for patients worldwide. The Breda site is a large-scale manufacturing operation focused on the assembly, inspection, labeling and packaging of pharmaceutical products. The site operates in a highly regulated GMP environment, where reliable equipment, automation and data integrity are essential to maintaining safe, compliant and efficient production.   About the position We are looking for a Senior Automation Engineer to join the Equipment Engineering team in Breda. In this role, you will take ownership of the automation side of new and upgraded manufacturing equipment — from design and vendor testing through installation, qualification and operational handover. You will work closely with Engineering, Manufacturing, Maintenance, IT and external equipment suppliers to make sure automation systems are reliable, secure, compliant and ready for production. This is a hands-on role for someone who enjoys combining automation engineering, project execution and troubleshooting in a regulated manufacturing environment.   Responsibilities Lead the automation activities for new and upgraded manufacturing equipment. Review and develop automation design documentation, including URS, FDS, HDS…

The Company Our client is a global leader in advanced cell therapy, specializing in developing and delivering cutting-edge treatments for patients with serious illnesses. The organization operates state-of-the-art manufacturing facilities and follows the highest GMP standards to ensure quality and safety. Role Description As a Senior Quality Systems Specialist, you are responsible for governing and improving key GMP Quality Systems, ensuring processes remain compliant, robust, and inspection-ready. You will work closely with Quality, Operations, and cross-functional stakeholders at site and cross-site level. Responsibilities – Manage and support Quality Systems including Change Control, Deviations, CAPA, and MRB. – Maintain and improve quality procedures and coordinate site training. – Monitor compliance, quality metrics, and management review inputs. – Identify and manage quality risks in line with EU GMP, ICH Q10, and internal policies. – Chair or support multidisciplinary quality boards and committees. – Support audits and regulatory inspections, including preparation and follow-up. – Review and approve quality documentation, changes, deviations, and CAPAs. – Drive continuous improvement of quality processes, reporting, and automation. – Provide backup support to the Quality Systems Lead/Manager when…

Over het Bedrijf Deze internationale producent binnen de voedingsmiddelenindustrie beschikt over een belangrijke productielocatie in Nederland waar hoogwaardige zuivelproducten worden geproduceerd voor de wereldwijde markt. Veiligheid, duurzaamheid en continue verbetering staan centraal binnen de organisatie, waarbij de HSE-afdeling een essentiële bijdrage levert aan een veilige en gezonde werkomgeving. Rolomschrijving Als HSE Specialist ben je verantwoordelijk voor het verbeteren en waarborgen van de prestaties op het gebied van Health, Safety & Environment binnen de productielocatie. Je werkt nauw samen met productie, management en externe instanties om een sterke veiligheidscultuur te creëren, wet- en regelgeving na te leven en structurele verbeteringen door te voeren. Het is een zelfstandige functie waarbij je zowel zichtbaar bent op de werkvloer als verantwoordelijk bent voor beleidsmatige en administratieve werkzaamheden. Belangrijkste Verantwoordelijkheden Adviseren en ondersteunen van productie en management op het gebied van HSE Initiëren en begeleiden van veiligheids- en milieuverbeteringen Uitvoeren en begeleiden van risicoanalyses, incidentonderzoeken en opvolgacties Bewaken van naleving van HSE-wetgeving, vergunningen en managementsystemen Beheren van het bedrijfsnoodplan en coördineren van de BHV-organisatie Ondersteunen bij audits, inspecties en continuous improvement initiatieven Monitoren en rapporteren…

About the Company Join a leading biotechnology company at the forefront of immunotherapy and engineered T cell therapy, revolutionizing cancer treatment with individually tailored therapies. Located in Hoofddorp, our client offers a dynamic, fast-paced, and ever-evolving environment where groundbreaking discoveries are made daily. About the Position We are seeking a motivated QC Microbiology Analyst (Microbiologist I) to join a diverse and collaborative team. In this role, you will perform essential microbiological assays and environmental monitoring to support innovative cancer immunotherapies. You will report to one of the Team Leads QC Microbiology and work alongside a team of 20+ professionals. Responsibilities Conduct environmental monitoring of cleanrooms. Perform microbiological assays, including Gram Stain, Endotoxin, Sterility, Microbial Identification, Growth Promotion, Bioburden, and Plate Reading. Enter, review, and trend assay results data. Maintain lab equipment and lab spaces. Support various department projects. Perform additional duties as required. Requirements Vocational Training (MLO level 4) or a bachelor's degree in Microbiology preferred. 0 to 4 years of experience in a Microbiology lab or Environmental Monitoring. Proficient in microbiological techniques like air monitoring, water testing, surface monitoring,…