The Company Our client is a global healthcare company with a portfolio of therapies and products in women’s health, biosimilars, and established medicines across a wide array of conditions and diseases. Our mission is to deliver impactful medicines and solutions for a healthier every day.. Role Description We are seeking a dedicated Laboratory Specialist with expertise in materials characterization to join a dynamic team supporting global pharmaceutical projects. This role focuses on hands-on laboratory work involving the identification and analysis of unknown materials and particles, assisting in root cause investigations, and supporting scientific research activities within a fast-paced environment. Responsibilities -Conduct hands-on analytical testing using techniques such as FTIR, optical microscopy, Raman spectroscopy, SEM-EDX, and X-ray inspection. -Characterize unknown particles and materials, especially extraneous matter and packaging components. -Support global investigations into material defects, foreign particles, and other anomalies. -Collaborate on multiple international projects, executing experiments independently and supporting experimental design. -Prepare detailed technical reports documenting investigation findings, clearly presenting scientific conclusions in English. -Assist in root cause analysis related to drug products, excipients, and packaging materials. -Maintain laboratory equipment and ensure proper documentation of all activities. Requirements -Bachelor's, Master's, or equivalent in a scientific or technical discipline such as Materials Science, Analytical Chemistry, or Chemical Sciences. -Hands-on experience with techniques like FTIR, optical microscopy, Raman, SEM-EDX, and X-ray inspection. -Strong analytical skills with experience identifying unknown particles, foreign materials, or material defects. -Proven ability to work independently, troubleshoot, and handle multiple global projects simultaneously. -Excellent written communication skills in English for report writing and documentation. -Good teamwork, attention to detail, and ability to work under pressure. Other Information If you are interested and want to apply, please submit your application via the apply button below and contact me.

Associate Supply Chain Import/Export (Level 3) About the Company Join a leading global biotechnology company dedicated to improving patients' lives through innovative medicines. With a strong international supply chain network, the company ensures the reliable and compliant distribution of pharmaceutical products to patients worldwide. You'll be part of a collaborative, diverse team that values quality, continuous improvement, and operational excellence. About the Role As an Associate Supply Chain Import/Export (Level 3), you will coordinate the end-to-end movement of pharmaceutical products across global markets. You will manage customer orders, import/export documentation, shipment coordination, and logistics activities while ensuring compliance with GMP/GDP regulations and delivering exceptional customer service. Key Responsibilities Manage end-to-end customer orders and global import/export shipments. Prepare shipping documentation and monitor deliveries. Resolve logistics and transportation issues with internal teams and logistics partners. Coordinate product returns and support cross-functional supply chain projects. Ensure compliance with GMP/GDP standards and company procedures. Drive continuous process improvements and contribute to KPI reporting. Key Requirements Bachelor's degree with 2+ years of experience in Supply Chain, Logistics, Import/Export, or Customer Service, or a Master's degree in a relevant field. Experience within a GMP/GDP-regulated industry is preferred. Knowledge of international logistics, import/export operations, and ERP systems (SAP or similar). Strong communication, organizational, and problem-solving skills. Fluent in English with the ability to work effectively in an international environment. Other Information Are you interested in this or another role? click the apply button below and I will contact you as soon as possible.   

Company Overview: A leading cooperative in the dairy sector, dedicated to producing trusted and beloved brands used daily by millions. This organization combines a vibrant, international work environment with a strong focus on sustainability. They are committed to supporting employee growth through training, coaching, and internal development opportunities, enabling staff to make a meaningful impact with confidence and independence. Job Description: We are seeking an experienced Senior Maintenance Specialist to take technical ownership of part of a modern cheese manufacturing facility. This role demands a skilled professional with strong mechanical and electrical expertise, responsible for ensuring optimal maintenance and operational reliability of critical production equipment. Responsibilities: •    Take technical responsibility for a designated section of the plant’s machinery and systems. •    Serve as a knowledge expert in mechanical and electrical engineering. •    Analyze and resolve complex technical faults independently, prioritizing safety and efficiency. •    Plan, prepare, and coordinate maintenance activities carried out by internal technicians and external partners. •    Collaborate with production, planning, quality, and external suppliers to facilitate smooth maintenance operations. •    Investigate breakdowns and contribute to the development of maintenance strategies and improvement initiatives. •    Lead and develop a team of technicians, fostering their skills and knowledge to enhance overall technical competence. •    Drive continuous improvement efforts to increase reliability, availability, and performance of plant equipment. Requirements: •    At least 8 years’ technical experience with a relevant diploma (HBO level) or more than 4 years with a secondary vocational education (MBO level). •    Strong background in mechanical and electrical systems, preferably in food, dairy, or related industries such as chemie or pharma. •    Hands-on experience with mechanical, electrical, and control systems; practical tinkering is essential. •    Fluent in both Dutch and English, with excellent communication skills. •    Previous experience in a maintenance leadership or senior technician role would be advantageous. •    Ability to analyze problems independently and communicate effectively with both management and technical staff. •    Willingness to work approximately 38 hours per week; 32 hours considered for the right candidate. •    We are prioritizing continuous CV review and candidate screening to meet the current demand for seasoned technical profiles. Other Information: If you are interested and want to apply, please submit your application via the apply button below and contact me.

QC Microbiology Analyst (Microbiologist I) About the Company Join a leading global biotechnology company at the forefront of developing innovative cancer immunotherapies. You'll become part of a collaborative Quality Control Microbiology team dedicated to ensuring the highest standards of product quality and patient safety in a GMP-regulated manufacturing environment. Position Overview As a QC Microbiology Analyst, you will play a key role in monitoring and maintaining microbiological quality within cleanroom manufacturing areas. You will perform environmental monitoring, microbiological testing, data review, and laboratory support activities to ensure compliance with GMP and regulatory standards. Key Responsibilities Perform Environmental Monitoring (EM) in GMP cleanrooms. Conduct microbiological testing, including Sterility, Bioburden, Endotoxin, and Plate Reading. Record, review, and trend microbiological test results. Perform routine maintenance of laboratory equipment and work areas. Support laboratory projects and continuous improvement initiatives. Ensure compliance with GMP, SOPs, and quality standards. Candidate Profile Bachelor's degree or MLO Level 3 qualification in Microbiology or a related Life Sciences discipline. Experience in microbiology laboratories or environmental monitoring is preferred. Knowledge of microbiological techniques, including air, water, and surface monitoring. Experience working with aseptic techniques and cleanroom operations. Understanding of GMP regulations and Quality Control procedures. Proficiency in Microsoft Office (Word, Excel, and PowerPoint). Strong communication skills in English (Dutch is not required). Able to work in a fast-paced manufacturing environment and adapt to changing priorities. Additional Information Rotating 18-week shift schedule. Ability to work in cleanroom environments while wearing full gowning. Ability to lift up to approximately 12 kg. Excellent opportunity to develop your career within an innovative and growing biotechnology organization. Other Information  Are you interested in this or another role? click the apply button below and I will contact you as soon as possible.   

Company Our client is a well-established manufacturing organisation with a strong focus on safety, sustainability, and operational excellence. They offer a structured, professional environment where people are encouraged to improve processes, lead by example, and deliver results through teamwork and continuous improvement. Job Description For a manufacturing site in the Netherlands, our client is looking for a Stores & Facilities Team Leader (Manufacturing Site) to manage a team that supports Maintenance operations. This role combines hands-on leadership with process improvement, safety compliance, and people development. The Stores & Facilities Team Leader (Manufacturing Site) works closely with site leadership to ensure materials, equipment, and services are delivered safely, efficiently, and according to standards. Responsibilities The Stores & Facilities Team Leader (Manufacturing Site) will be responsible for: Leading the team that supports Maintenance through key service areas such as: - Stores & Receiving (inspection, inbound handling, storage, and issuing of MRO materials) - Kitting & staging of materials per work order - Safety shop activities (inspection, cleaning, repair of safety clothing/equipment, and related site safety support) - Managing distribution of PPE and supporting internal/external mail and printing needs - Coordinating general site facility services - Ensuring all activities are executed according to procedures and safety standards - Monitoring and improving work processes, team effectiveness, and day-to-day execution - Driving continuous improvement by analysing KPIs, trends, deviations, and operational bottlenecks, and translating these into practical improvement actions - Coaching and developing team members through performance management, feedback, and individual development plans - Managing key people-related topics such as planning, training, absence management, and performance reviews Requirements The ideal Stores & Facilities Team Leader (Manufacturing Site) has: - A completed HBO degree or the proven ability to operate at HBO level - Demonstrated experience leading and developing a team in a production, maintenance, logistics, or site services environment - Strong awareness of safety procedures and the discipline to work to standards in a regulated/industrial setting - A continuous improvement mindset (Lean experience is a strong advantage) - The ability to analyse data (KPIs, dashboards, tables) and convert findings into structured improvements - Strong communication skills and the ability to stay effective under pressure Other Information If you are interested and want to apply, please submit your application via the apply button below and contact me.  

Company Overview A global leader dedicated to sustainability, innovation, and excellence in chemical manufacturing. The company values diversity, inclusion, and safety while striving to make a meaningful impact through their innovative solutions. Job Description We are seeking a highly experienced Asset Care Manager to lead proactive maintenance and reliability initiatives at our client’s facility in Dordrecht. The successful candidate will oversee the development and execution of strategic asset management programs to optimize operational performance, safety, and environmental standards. Responsibilities -Lead a team of around 10 specialists, including Maintenance Engineers, Reliability Engineers, and a Turnaround Coordinator. -Develop, implement, and continuously improve the Asset Care program to meet global objectives -for Overall Equipment Effectiveness (OEE), environmental compliance, efficiency, and safety. -Manage day-to-day escalations related to corrective maintenance issues. -Monitor, analyze, and report on key performance indicators (KPIs), communicating progress and challenges to stakeholders. -Build, develop, and motivate a high-performing team, fostering a culture of continuous improvement and safety. -Ensure adherence to best practices in maintenance and reliability, including Root Cause Failure -Analysis (RCFA), FMEA, 5-Why analysis, Non-Destructive Testing (NDT), and Condition-Based Monitoring. -Collaborate effectively with local and global teams to align maintenance strategies and organizational goals. Requirements -Bachelor’s or master’s degree. -Over 10 years’ experience in Maintenance, Reliability, or Turnarounds. -Proven leadership experience, managing teams of at least five people, with a strong background in change management. -Knowledge of reliability tools like RCFA, FMEA, 5-Why, NDT, and Condition-Based Monitoring. -Strong stakeholder management skills, both locally and globally. -Good understanding of Maintenance Excellence principles and Total Productive Maintenance (TPM). -Excellent communication skills in English and Dutch. Other Information If you are interested and want to apply, please submit your application via the apply button below and contact me.  

The company Our client is a leader in immunotherapy and engineered T cell therapy, driving innovation in cancer treatment. They are transforming the landscape with personalized, patient-specific therapies. Role Description As a QC Microbiology Analyst, you'll be part of a diverse team of 20+ Analysts, Senior Analysts, and Lead Analysts, reporting to one of the Team Leads in QC Microbiology. Your role involves performing various microbiological assays, environmental monitoring of cleanrooms, data entry and review, and supporting department projects in a fast-paced, collaborative work environment. Knowledge of GMP, aseptic techniques, and microbiological processes are essential for success. Responsibilities - Perform environmental monitoring of cleanrooms.  - Conduct microbiological assays such as Gram Stain, Endotoxin, Sterility, Microbial Identification, Growth Promotion, Bioburden, and Plate Reading.  - Data entry, review, and trending of assay results.  - Perform routine maintenance of lab equipment and lab spaces.  - Support department projects.  Requirements - MLO level 4 (Vocational Training) or a Bachelor's degree in Microbiology preferred.  - 0 to 4 years of Microbiology lab/Environmental Monitoring experience.  - Experience with microbiological techniques such as air monitoring, water testing, surface monitoring, and genus/species identification of microorganisms.  - Knowledge of aseptic techniques and clean room operations.  - Ability to gown for clean room entry and lift approximately 12Kg.  - Familiarity with GMP regulations and quality control processes.  - Proficiency in MS Word, Excel, PowerPoint, and other applications.  Other Information Apply to our vacancy for more. Looking forward to chatting with you!  

Over het Bedrijf Deze internationale farmaceutische organisatie ontwikkelt en produceert geneesmiddelen voor patiënten wereldwijd. Binnen Pharmaceutical Technical Operations (PTO) werken multidisciplinaire engineeringteams aan de implementatie van nieuwe verpakkingstechnologieën, procesoptimalisatie en het waarborgen van GMP-compliance binnen de productieomgeving. Rolomschrijving Als Packaging Equipment Engineer ben je verantwoordelijk voor de technische ondersteuning van verpakkingsprocessen en -apparatuur binnen de farmaceutische productie. Je werkt aan de introductie van nieuwe technologieën, kwalificatie van apparatuur en procesverbeteringen. Daarnaast speel je een belangrijke rol in technische onderzoeken, CAPEX-projecten en het waarborgen van kwaliteit, veiligheid en compliance binnen een GMP-omgeving. Belangrijkste Verantwoordelijkheden Implementeren, kwalificeren en optimaliseren van farmaceutische verpakkingsapparatuur en -processen Opstellen en uitvoeren van technische documentatie, waaronder URS'en, risicoanalyses, kwalificatieprotocollen, rapportages en projectplannen Leiden en uitvoeren van technische onderzoeken, root cause analyses, wijzigingen en CAPEX-projecten Coördineren van kwalificatie- en validatieactiviteiten van verpakkingsapparatuur Initiëren en realiseren van proces- en technologieverbeteringen binnen de verpakkingsomgeving Werken volgens QMS-, GMP-, SHE- en change control-processen Intensief samenwerken met Operations, Quality, Engineering, Regulatory Affairs, Supply Chain en andere stakeholders Deelnemen aan of leiding geven aan technische expertgroepen binnen Packaging Vereisten Enkele jaren relevante werkervaring binnen de farmaceutische industrie of een andere sterk gereguleerde productieomgeving Ervaring met apparatuurkwalificatie, validatie en technische documentatie Kennis van secundaire en tertiaire farmaceutische verpakkingstechnieken en verpakkingsmaterialen Goede kennis van GMP, EHS/SHE en Lean-principes Sterke analytische vaardigheden en ervaring met root cause analyses Goede communicatieve vaardigheden en stakeholdermanagement Uitstekende beheersing van zowel de Nederlandse als Engelse taal

The Company Our client is a global healthcare company with a portfolio of therapies and products in women’s health, biosimilars, and established medicines across a wide array of conditions and diseases. Our mission is to deliver impactful medicines and solutions for a healthier every day. Role Description As an Associate Scientist, you will be responsible for performing hands-on material characterization and analytical investigations to support pharmaceutical products and packaging. You will utilize advanced analytical techniques to identify and resolve product-related issues, contribute to root cause investigations, and support laboratory activities that ensure product quality, compliance, and continuous improvement. Responsibilities Conduct hands-on analysis using techniques such as SEM-EDX, FTIR, Raman spectroscopy, optical microscopy, tensile and compression testing, and X-ray inspection to support projects focused on extraneous matter and packaging. Assist in organizing and executing global laboratory activities within a pharmaceutical environment, ensuring compliance with quality standards. Support investigations into pharmaceutical materials, root cause analysis, and characterization of drug products and raw materials. Prepare technical investigation reports and document findings clearly and accurately. Collaborate with cross-functional teams to troubleshoot and resolve material-related issues. Requirements Bachelor’s degree with hands-on laboratory experience, preferably in pharmaceutical, physical, chemical, or analytical sciences. Experience with research, development, manufacturing, or testing of pharmaceutical products is a plus. Familiarity with analytical techniques such as SEM-EDX, FTIR, Raman, microscopy, and mechanical testing. Ability to write technical reports and communicate effectively in English. Capable of working independently, taking responsibility, and performing under pressure. Other Information Apply to our vacancy for more information. looking forward to hearing from you.

The Company A global manufacturing organization operating within supply chain and production environments, focused on digital transformation and process optimization. The company drives innovation through advanced planning systems, cross-functional collaboration, and large-scale implementation programs across international sites. Role Description This role focuses on leading the deployment of key supply chain systems across international manufacturing locations. You will act as the bridge between central teams and local plant operations, ensuring successful implementation and adoption of planning tools. The position combines project management, stakeholder engagement, and hands-on support during critical deployment phases. Responsibilities - Lead deployment of supply chain systems including scheduling and planning tools. - Translate central implementation requirements into local execution plans. - Support plant teams in production, quality, maintenance, and planning. - Coordinate closely with stakeholders across multiple regions. - Drive readiness for system go-live and ensure smooth transition. - Act as the key link between headquarters and plant operations. - Support training, system adoption, and user alignment. - Monitor progress and address operational challenges during deployment. Requirements - Strong project management experience. - Experience with system implementations in large organizations. - Knowledge of SAP and OMP systems. - Background in supply chain, production, or manufacturing environments. - Ability to influence and energize cross-functional teams. - Strong communication skills in English. - Willingness to travel internationally for extended periods. - Experience working with stakeholders across multiple functions. - Ability to operate in dynamic and fast-paced environments. Other Information Travel Frequent travel to the United States for key project phases