The Company The client is a Dutch/Belgian food manufacturing company focused on frozen snacks, meal components, and private-label food products across Europe. Role Description As a Senior QA Officer, you will play a key role within a close-knit quality team of four, supporting the maintenance and continuous improvement of quality standards across the production sites in Venlo and Belfeld. This is a senior-level position where you will act as the right-hand to the QA (QE) Manager, contributing both strategically and operationally to quality assurance activities. You will work in a fast-paced, dynamic environment where no two days are the same, ensuring that quality and food safety remain central to all processes. Acting as a link between multiple departments, you will help embed a strong quality culture throughout the organization. Responsibilities Maintaining and updating quality systems and the quality handbook in collaboration with the QE Manager. Monitoring and handling internal and external complaints related to production. Managing product holds and following up on quality-related process deviations. Conducting inspections on products and production processes. Organizing and executing internal audits and hygiene checks. Preparing, reviewing, and maintaining product specifications and documentation.…

The Company The client is part of the global pharmaceutical company. The facility is focused on the development and manufacturing of biologic medicines, particularly in the fields of immunology, oncology, and infectious diseases. They specialize in producing large-scale biologic drugs, which are typically made from living cells and are used to treat complex diseases.  Role Description The Junior Quality Engineer is responsible for leading and coordinating investigations related to quality issues within manufacturing processes, systems, and products. The role focuses on identifying root causes, ensuring effective corrective and preventive actions (CAPA), and maintaining compliance with internal standards and regulatory requirements. Working cross-functionally with operations and quality teams, the Quality Engineer drives continuous improvement, ensures accurate documentation, and communicates outcomes to key stakeholders. This position requires strong analytical capabilities, attention to detail, and the ability to manage complex investigations with a high level of independence and professionalism. Responsibilities Leading and managing quality investigations, including non-conformances, CAPAs, and change controls, from initiation through completion. Applying in-depth knowledge of quality regulations and standards to support the handling and closure of quality records. Assembling and guiding cross-functional teams for investigation…

Company A reputable organisation in the manufacturing and engineering space, known for high standards, strong teamwork, and a continuous improvement mindset. Quality, compliance, and clear ways of working are key to how they deliver reliable products and services. Job Description We are looking for a Quality Engineering Specialist (Dutch & English Speaking) to support quality performance on-site in Leiden. The role focuses on ensuring products and processes meet defined specifications through inspections, testing, strong documentation, and effective collaboration with engineering and production teams. The successful candidate will help investigate quality issues, drive improvements, and support audit and compliance activities. Responsibilities – Carry out quality inspections and testing to confirm compliance with specifications and standards – Work closely with engineering and production teams to investigate issues and identify root causes – Support corrective actions and help prevent recurrence through structured problem solving – Prepare, maintain, and improve quality documentation (procedures, reports, records) – Contribute to continuous improvement initiatives to strengthen quality and efficiency – Support audit readiness and participate in compliance-related activities – Communicate clearly with stakeholders in both Dutch and English Requirements –…

Company: Our client is an international organization operating in a highly regulated environment, focused on delivering high-quality products that support people’s health and well-being. The site in the Netherlands works in close collaboration with global teams and offers a professional setting where quality, compliance, and continuous improvement are key. Job Description: For this assignment, we are looking for a Quality Engineering Specialist to strengthen the Quality Engineering team on site in Leiden. The Quality Engineering Specialist supports day-to-day quality activities, helps maintain high compliance standards, and works closely with stakeholders across operations, engineering, and quality. The role requires strong communication skills in English; knowledge of Dutch is a plus. Responsibilities: – Support quality engineering activities in a regulated production environment – Help ensure quality processes and documentation remain compliant and up to date – Collaborate with cross-functional teams to support smooth execution of operational quality topics – Contribute to continuous improvement initiatives within quality processes – Communicate clearly with stakeholders and follow up on actions to completion Requirements: – Experience in Quality Engineering (or a closely related quality/assurance role) – Professional working proficiency in English (Dutch is an advantage) –…

The Company  The company is a global biotechnology company dedicated to improving the lives of patients. In Breda they focus on preparing, planning, and coordinating the shipping and distribution of clinical trial materials.  Role Description The Temporary Manufacturing Technician supports operations within the manufacturing department as part of a central flexible workforce. This temporary position (7-month maternity cover) involves working across multiple production lines, including automated, semi-automated, and manual setups, within a 2- or 3-shift schedule. Responsibilities Operating production lines in accordance with standard operating procedures (SOPs) and GMP guidelines. Ensuring daily targets related to safety, quality, delivery, and efficiency are met. Maintaining accuracy, discipline, and adherence to defined workflows and production speeds. Collaborating closely with operators and Line Leads to achieve operational objectives. Switching effectively between production lines and tasks as required. Identifying and supporting continuous improvement initiatives within processes and workflows. Escalating issues in a timely and structured manner to the Line Lead (Tier 1 level). Taking ownership of assigned tasks and results, demonstrating accountability and professionalism. Actively participating in shift handovers to ensure continuity of operations. Ensuring all required training is completed within defined…

The Company A global organization in the pharmaceutical and biologics manufacturing sector, focused on maintaining high-quality standards, regulatory compliance, and continuous improvement across production processes. The company operates in a highly regulated environment with a strong emphasis on innovation, patient safety, and operational excellence. Role Description The Senior Quality Engineer acts as an Investigation Owner, leading complex quality investigations across manufacturing operations. The role focuses on identifying root causes, driving corrective and preventive actions, and ensuring compliance with regulatory and internal standards. You will collaborate cross functionally, oversee quality records, and contribute to continuous improvement initiatives. This position is ideal for a seasoned professional with strong analytical thinking and leadership capabilities. Responsibilities – Lead nonconformance investigations including CAPA and change control activities from initiation to closure. – Apply expertise in quality requirements to manage and support quality records. – Review and approve documentation related to manufacturing processes and operations. – Ensure accurate, compliant, and timely completion of quality records. – Maintain and update procedures aligned with regulatory and internal requirements. – Drive risk mitigation strategies and continuous improvement initiatives. –…