Company We are looking for candidates for a site engineering team supporting pharmaceutical technical projects within a regulated GMP environment. Job Description This role is for a CQV Commissioning Qualification Validation Engineer (GMP). The engineer will support technical projects with minimal supervision and report to the Senior Manager Validation & Compliance. You will take a hands-on approach to commissioning and qualification activities, develop and execute test strategies, and drive the creation of system commissioning qualification and validation documentation. Responsibilities – Develop and update validation documentation, including system-level criticality assessments, validation and commissioning/qualification plans, risk assessments, test protocols, and requirement traceability matrices – Prepare and maintain commissioning, qualification, and validation summary reports – Lead commissioning, qualification, and validation activities for technical solutions – Provide technical guidance to project teams to ensure implemented solutions follow the validation plan and meet internal customer requirements – Support delivery in line with established site procedures (SOPs) – Carry out additional tasks or projects as requested by your supervisor Requirements – At least 3 years of experience executing commissioning, qualification, and validation within pharmaceutical manufacturing – Hands-on commissioning and qualification experience in secondary packaging…

About the Company A leading global biotechnology organization focused on developing and manufacturing innovative medicines for patients worldwide. Operating in a highly regulated GMP environment, the company continuously invests in advanced manufacturing technologies, engineering projects, and operational excellence to support its growing product portfolio. Role Description We are looking for a CQV Engineer to support commissioning, qualification, and validation activities within a GMP manufacturing environment. In this role, you will be responsible for developing validation documentation, leading testing activities, and ensuring that new and modified systems are implemented in compliance with internal quality standards and regulatory requirements. The position requires a hands-on validation professional with experience in secondary packaging systems and computerized systems validation. Key Responsibilities Develop and maintain CQV documentation, including plans, protocols, risk assessments, and summary reports. Lead commissioning, qualification, and validation activities for manufacturing systems. Support the implementation of technical solutions in accordance with validation requirements. Perform system risk assessments and requirement traceability activities. Execute and document testing activities within GMP environments. Provide validation guidance to project teams and stakeholders. Ensure compliance with internal procedures and regulatory…

The Company The client is a French multinational that has an R&D-driven presence in the Netherlands, focusing on the research, development, and manufacturing of pharmaceutical products and vaccines, including treatments for oncology, cardiology, and rare diseases.  Role Description A global healthcare leader is seeking a Pharmacovigilance Associate to join its team in the Netherlands. This role focuses on ensuring patient safety through the effective management and evaluation of pharmacovigilance (PV) data. Operating within a diverse and cross-functional environment, you will contribute to safeguarding public health while gaining exposure to a broad product portfolio across multiple therapeutic areas. As part of the North Europe Multi-Country Organization, you will collaborate closely with regional and local teams, supporting pharmacovigilance activities in compliance with local regulations and internal policies. The position also plays a key role in maintaining strong relationships with stakeholders and promoting awareness of PV requirements across the business. Responsibilities Managing personal workload effectively, ensuring timely delivery of pharmacovigilance activities. Handling and process Individual Case Safety Reports in line with regulatory requirements and company procedures. Conducting case assessments and ensuring accurate data entry and reporting. Monitoring…

Company: A global food and nutrition organization with strong roots in dairy production, focused on delivering high-quality products through innovation, sustainability and operational excellence. The company operates across multiple international markets with complex supply chain networks. Job Description: This is a high-impact interim procurement role focused on capital expenditure projects across a regional European scope. The position requires taking full ownership of multiple sourcing initiatives, ensuring timely delivery, cost efficiency and adherence to quality standards. You will be driving tender processes, negotiations and supplier engagement while operating in a fast-paced, high-pressure environment. Responsibilities: – Lead and execute CapEx sourcing projects and supplier negotiations across multiple ongoing initiatives – Prepare and manage RFQ processes, evaluate proposals and finalize procurement contracts – Ensure project delivery within timelines, budget and quality requirements – Manage multiple stakeholders, suppliers and projects simultaneously while maintaining clear priorities – Drive compliance with procurement policies, processes and contract standards – Support and implement regional sourcing strategies and align with global category teams – Identify risks, cost-saving opportunities and potential bottlenecks in projects – Strengthen relationships with suppliers and…

The Company The client is one of the Netherlands’ biggest dairy products manufacturers who is also active globally.    Role Description We are seeking an O2C Customer Service Specialist to join a leading multinational in the dairy industry based in Amersfoort. In this role, you will act as a key point of contact for customers, ensuring the smooth execution of the entire order-to-cash cycle. You will work cross-functionally with internal stakeholders to deliver high-quality service, maintain strong client relationships, and support operational excellence within the commercial function. Responsibilities  Managing the end-to-end order-to-cash process, including order entry, order validation, and invoicing. Serving as the primary contact for customer inquiries related to orders, deliveries, and account status. Ensuring accurate and timely processing of customer orders in line with company policies. Collaborating with supply chain, logistics, and finance teams to resolve order or billing issues. Monitoring order fulfillment and proactively communicating delays or discrepancies to customers. Handling customer complaints professionally and driving timely resolution. Maintaining and updating customer data in internal systems to ensure accuracy. Supporting continuous improvement initiatives within the O2C process to optimize efficiency and service quality. Ensuring compliance with internal controls, procedures,…

Company A global healthcare business focused on improving prevention, treatment, and patient outcomes through science and innovation. Job Description We are looking for a Pharmacovigilance Officer (Junior) to support patient safety within a cross-functional team in Amsterdam. This role focuses on accurate and timely handling of pharmacovigilance information, assisting with assessment of incoming safety data, and helping to identify any emerging safety, quality, or regulatory concerns. Responsibilities – Manage your own workload and ensure timely processing of incoming pharmacovigilance information – Handle inbox management and support case assessment and processing activities – Follow up with relevant reporters (including patients, healthcare professionals, and associated vendors) to obtain additional details needed for case assessment – Ensure potential safety, quality, and regulatory issues are identified quickly and escalated appropriately – Support compliance activities and maintain local pharmacovigilance quality documentation – Contribute to educational materials management – Participate in safety data review to spot trends, clusters, and pattern variances – Provide pharmacovigilance training to key stakeholders (both internally and externally) Requirements – Approx. 2 years of relevant experience in pharmacovigilance or a closely related safety role – Dutch required…