Company Our client is a leading organisation in the life sciences sector, operating in a highly regulated manufacturing environment. They develop and produce innovative therapies and are known for strong quality standards, continuous improvement, and cross-functional collaboration across technical and operational teams. Job Description For our client in Leiden, we are looking for a Process Engineer – Biopharma Manufacturing Support (Leiden). The role supports manufacturing operations by improving process performance, helping resolve process-related issues, and working closely with stakeholders to ensure safe, compliant, and efficient production. Responsibilities – Support daily manufacturing operations by investigating and resolving process-related issues – Identify improvement opportunities and contribute to process optimisation initiatives – Collect, analyse, and interpret process data to support decision-making and performance tracking – Work cross-functionally with operations, quality, and technical stakeholders to align on priorities and actions – Contribute to documentation and standard ways of working to support a regulated environment – Participate in improvement projects and support implementation of changes on site Requirements – Background in process engineering within an industrial or manufacturing environment – Experience in a regulated setting (life sciences is a strong advantage)…

About the Company An international medical technology organization focused on developing and manufacturing innovative healthcare solutions that improve patient care worldwide. The company operates in a highly advanced and regulated production environment where technology, quality, and continuous improvement are central to daily operations. Role Description As Product Industrialization Engineer, you will play a key role in the successful industrialization and introduction of new products within a high-tech manufacturing environment. You will work in multidisciplinary project teams and act as the link between product development and manufacturing, ensuring a smooth and efficient transition from design to production. This role requires a technically strong and proactive engineer with experience in process development, validation, automated equipment, and manufacturing optimization within complex production environments. Key Responsibilities Participate in New Product Introduction (NPI) projects and ensure manufacturability of new products and processes. Design and optimize production processes, assembly flows, and testing solutions for manufacturing environments. Perform technical risk assessments using methodologies such as pFMEA and support continuous improvement initiatives. Define manufacturing, equipment, and process requirements based on product specifications and factory standards. Coordinate development, sourcing,…

The Company A global pharmaceutical organization focused on developing, producing and commercializing vaccines and antibody-based solutions to fight infectious diseases. The site operates in a highly innovative, fast-paced environment with strong emphasis on technical excellence, compliance and continuous improvement. Role Description We are looking for an experienced Senior EHS Engineer – Engineering & Maintenance to join a leading global healthcare organization within a highly regulated GMP environment. In this role, you will act as the main safety contact for multidisciplinary engineering and facility projects, ensuring safe execution, regulatory compliance, and continuous improvement of site safety standards while collaborating closely with engineers, contractors, maintenance teams, and project stakeholders. Responsibilities – Lead EHS and safety activities during engineering, maintenance, and facility upgrade projects. – Develop and manage work permits, risk assessments, LOTOTO procedures, and safety plans. – Supervise contractors and on-site activities to ensure safe and compliant execution. – Conduct safety inspections, audits, and incident investigations. – Support implementation and improvement of safety systems and procedures. – Deliver safety training and coach teams to strengthen the site safety culture. – Collaborate with cross-functional teams…

The Company Our client is a global health care company that delivers innovative health solutions through its prescription medicines, vaccines, biologic therapies, and animal health products. Its first European branch opened in Amsterdam and now has three other facilities in the Netherlands, serving countries all over the globe. Job Description Our client is seeking a proactive HR Data Analyst to join their Human Resources team. The successful candidate will provide administrative and tactical support, ensuring smooth HR operations and database management. Responsibilities – Input and update employee information in HR databases accurately according to guidelines. – Collaborate with managers and HR colleagues to coordinate tasks and ensure deadlines are met. – Support HR-related projects by assisting with various administrative tasks. – Work with moderate supervision, demonstrating knowledge and skills relevant to the role. – Provide general administrative support to the HR department as needed. Requirements – Proficiency in MS Office (Word, Excel, Outlook). – Strong organizational and administrative skills. – Excellent interpersonal and communication skills. – Ability to work with moderate supervision and prioritize tasks effectively. Other Information If you…

The Company Our client is a global biotechnology company focused on developing innovative antibody-based therapies to treat cancer and other serious diseases. With a strong international presence, they collaborate with leading pharmaceutical partners and are known for advancing cutting-edge science to improve patient outcomes. About the Role: The Medical Advisor supports clinical trials by providing medical and scientific expertise to study teams and stakeholders across the North Europe cluster. The role focuses on ensuring patient safety, scientific integrity, and operational feasibility throughout the clinical trial process. Responsibilities include advising on study protocols, feasibility assessments, stakeholder collaboration, and engaging with investigators and Key Opinion Leaders. Responsibilities: – Provide medical and scientific expertise to clinical trial teams to ensure patient safety and scientific integrity throughout the study lifecycle.  – Support study design, protocol development, feasibility assessments, patient recruitment strategies, and site selection activities.  – Act as the primary medical contact for investigators, clinical sites, and internal stakeholders including CSU, R&D, and Medical Affairs teams.  – Build and maintain strong relationships with Key Opinion Leaders (KOLs) to facilitate scientific exchange, gather study insights,…

The Company Our client is a  global leader in healthcare technology focused on developing advanced medical systems, diagnostic solutions, and patient-centered innovations that improve healthcare outcomes worldwide. Role Description We are seeking a skilled Product Industrialization Engineer  to join their team in Best. This role involves leading the transition of new medical products from development to manufacturing, ensuring processes are optimized for reliable, efficient, and high-quality production.  Responsibilities -Collaborate with product design teams during the development phase to ensure new products are designed with manufacturing and assembly considerations in mind. -Develop and validate production processes for new product introductions, including risk assessments like pFMEA. -Define Equipment, Process, and Manufacturing Requirements based on product specifications, test requirements from R&D, and factory standards. -Coordinate the sourcing, development, and installation of equipment and tools necessary for manufacturing. -Validate production processes and equipment through execution of pilot runs and Process Performance Qualification (PPQ). -Support ramp-up activities and assist in troubleshooting until processes are stable for mass production. -Manage manufacturing BOM and routing master data, ensuring accurate updates and changes according to PDLM guidelines. -Lead…