The Company Our client is a leading global Animal Health organization dedicated to improving the health and well-being of animals through innovative pharmaceuticals, vaccines, and health management solutions. The company offers an international working environment with excellent opportunities for professional growth, collaboration, and continuous learning. Role Overview We are looking for a Quality Assurance Specialist to support quality master data management and ensure compliance with GMP and regulatory standards. In this role, you will work closely with cross-functional teams to maintain quality systems, support process improvements, and contribute to operational excellence. Key Responsibilities Maintain quality master data in SAP, LIMS, and other quality systems. Ensure compliance with GMP, GDocP, and internal quality procedures. Process regulatory changes and support quality system improvements. Collaborate with cross-functional teams to resolve quality issues and improve processes. Requirements HBO degree in Life Sciences, Biochemistry, Microbiology, or a related field. Experience with SAP; LIMS knowledge is an advantage. Understanding of GMP and Good Documentation Practices (GDocP). Fluent in Dutch and English with strong communication skills. Other Information Interested in this opportunity or exploring other roles? Click…

  About Our Client Our client is one of the world’s leading biotechnology companies, dedicated to developing innovative medicines that improve the lives of patients worldwide. Their international supply chain organization plays a vital role in ensuring these medicines reach healthcare providers and patients safely, efficiently, and on time. Working in a highly regulated GMP/GDP environment, you’ll join a collaborative team that values quality, continuous improvement, and operational excellence. About the Position As an Associate Supply Chain Import/Export, you will be responsible for coordinating the international movement of pharmaceutical products from manufacturing sites to customers around the globe. You’ll oversee the complete order-to-delivery process, working closely with logistics providers, manufacturing sites, distributors, and internal stakeholders to ensure shipments are delivered accurately and on schedule. This role combines supply chain coordination, customer service, and international logistics in a fast-paced global environment. Key Responsibilities Coordinate international import and export shipments from order through delivery Process daily supply orders and ensure accurate execution Prepare and manage shipping and export documentation Monitor shipments proactively and resolve transportation or service issues Coordinate product returns and…

The Company Our client is a global biopharmaceutical company committed to advancing innovative medicines that improve patients’ lives worldwide. Through cutting-edge research, advanced biologics manufacturing, and a strong focus on quality and innovation, the company delivers life-changing therapies across a wide range of therapeutic areas. Role Description As a MSAT Validation Engineer, you will plan, coordinate, and execute validation and qualification activities for biopharmaceutical manufacturing processes, including mixing, sterilization, and buffer/microbial hold time studies. You will ensure GMP compliance by preparing validation documentation, supporting process improvements, and driving performance qualification activities for clinical and commercial drug substance production. Responsibilities Plan, coordinate, and execute validation and qualification activities for biopharmaceutical manufacturing processes. Prepare, review, and maintain validation protocols, reports, and GMP-compliant documentation. Perform and support sterilization, mixing, and cleaning validation activities to ensure regulatory compliance. Collaborate with Operations, Quality, and cross-functional teams to execute validation projects and support change controls. Drive process improvements and provide technical support to the MSAT team during validation and qualification activities. Ensure all validation activities comply with GMP standards and applicable regulatory guidelines. Requirements Bachelor’s or…

Company A leading global healthcare and pharmaceutical organization committed to delivering high-quality medicines through a reliable, compliant, and efficient global supply chain. The company values operational excellence, continuous improvement, and collaboration to ensure products reach patients worldwide. Role Description We are looking for a proactive Supply Chain Coordinator to support global import and export operations within a GMP/GDP-regulated environment. In this role, you will coordinate international shipments, manage order execution, ensure accurate documentation, and collaborate with internal teams and logistics partners to maintain an efficient and compliant supply chain. Responsibilities – Process customer orders and manage import/export documentation. – Coordinate international shipments and monitor deliveries. – Resolve transportation, service, and logistics-related issues. – Collaborate with third-party logistics providers, distributors, and internal stakeholders. – Support order-to-cash activities and maintain accurate ERP records. – Ensure compliance with GMP/GDP and company procedures. – Identify and implement process improvements to enhance supply chain performance. – Monitor KPIs and contribute to continuous improvement initiatives. – Support cross-functional projects and supply chain planning activities. Requirements – Bachelor’s or Master’s degree with 2+ years of supply chain…

About Our Client Our client is a global biotechnology company pioneering the future of cell therapy by developing innovative treatments for patients with cancer. Their cutting-edge manufacturing facility in Hoofddorp is dedicated to producing personalized cell therapies in a highly controlled GMP environment. Here, science, technology, and teamwork come together to deliver life-changing medicines while providing employees with excellent opportunities to develop their careers in advanced biopharmaceutical manufacturing. About the Position As a Manufacturing Technician for cell therapy, you will be part of the Manufacturing team responsible for producing personalized cell therapy products. Depending on business needs and after completing your training, you’ll work within either the Production Team or the Production Support Team, ensuring manufacturing activities are carried out safely, efficiently, and in full compliance with GMP requirements. This hands-on role offers the opportunity to work in state-of-the-art cleanrooms using advanced manufacturing processes that directly impact patient care. Key Responsibilities Perform manufacturing and production support activities within GMP cleanroom environments Execute manufacturing processes by following batch records, SOPs, and work instructions Prepare materials, media, and equipment required for production Support…

About Our Client Our client is a global biotechnology company at the forefront of cell therapy, developing innovative treatments that are transforming the way cancer is treated. Their state-of-the-art manufacturing facility in Hoofddorp combines science, engineering, and advanced manufacturing to produce life-changing therapies in a highly regulated GMP environment. Employees have the opportunity to work alongside multidisciplinary teams while contributing directly to products that make a real difference for patients worldwide. About the Position As a Process Engineer, you will join the Manufacturing Operations & Compliance Support (MOCS) team within MSAT, where you’ll provide technical support to commercial manufacturing. You’ll play a key role in ensuring manufacturing processes remain robust, compliant, and efficient by investigating process deviations, supporting product release activities, driving continuous improvements, and implementing sustainable solutions. This is a highly collaborative position where you’ll work closely with Manufacturing, Quality, Validation, and Engineering teams. Key Responsibilities Perform technical assessments to support manufacturing and product release Lead investigations into process deviations and identify root causes Develop and implement effective CAPAs to prevent recurrence Support process optimization and continuous improvement projects…