Life Sciences Consultancy & Project Management in Netherlands

The Company Our client is a well-known global dairy cooperative with over 150 years of experience in delivering high-quality dairy products and nutritional solutions worldwide. Role Description As a Customer QA Manager, you’ll act as the key quality partner for customers, managing complex quality topics and translating customer requirements into practical internal solutions. You’ll work closely with QA, R&D, Regulatory, Operations and Sales while driving customer satisfaction and continuous improvement. Responsibilities – Serve as the main point of contact for customer quality inquiries and issues – Lead and coordinate complex customer cases and quality requests – Translate customer quality requirements into internal standards and ensure alignment across Operations, R&D, Regulatory, and Sales teams – Build and maintain strong relationships with key customer stakeholders to foster long-term partnerships based on trust – Ensure products and processes meet internal standards, regulatory requirements, and customer expectations – Analyse customer feedback and quality data to identify trends and implement continuous improvements – Drive initiatives for quality assurance and innovation based on customer insights Requirements – Master’s degree in Food Technology, Life Sciences, or a…

Company Our client is a global organisation operating in a highly regulated pharmaceutical manufacturing environment. The site combines production and quality expertise to ensure products are made safely, consistently, and in full compliance with GMP and internal quality standards. The culture values ownership, clear documentation, and practical collaboration between Quality and Production. Job Description We are looking for a Deviation Investigator to support a production organisation by managing deviations and leading quality investigations to timely closure. The focus of this role is on quality-system investigations rather than routine production work. The successful candidate will be analytical, structured, and confident working independently while partnering closely with Production stakeholders. Responsibilities – Write, manage, and coordinate deviations from start to closure. – Lead quality investigations, including defining scope, gathering evidence, and documenting findings. – Perform root cause analysis and support the definition and follow-up of corrective and preventive actions (CAPAs). – Work closely with Production teams to clarify facts, challenge assumptions when needed, and keep investigations moving. – Ensure investigation files are complete, traceable, and compliant with GMP and internal quality standards. – Review…

The Company A global leader in nutrition and food ingredients, supplying high quality solutions to customers across the food, beverage, and health sectors. The organization operates internationally and focuses on innovation, quality, sustainability, and customer satisfaction. About the Role We are seeking a senior Customer QA Manager to act as the primary quality partner for customers across Europe. In this role, you will bridge the gap between customer expectations and internal quality standards, ensuring product quality, compliance, and customer satisfaction. You will manage complex customer quality topics, build strong relationships, and drive continuous improvement initiatives across the business. Responsibilities Act as the main Quality Assurance contact for customers Lead and coordinate complex customer quality cases and escalations Translate customer quality requirements into internal standards and processes Ensure compliance with customer requirements and applicable regulations Analyse customer feedback and quality data to identify improvement opportunities Drive continuous improvement initiatives within Customer QA Represent quality during customer meetings and audits Support the development and execution of Customer QA strategy Requirements Master’s degree in Food Technology, Life Sciences, or a related field Minimum…

The Company A leading pharmaceutical manufacturing organization focused on producing high quality medicines in a highly regulated environment. The company emphasizes quality, compliance, continuous improvement, and operational excellence across its production activities. About the Role This role is responsible for supporting and maintaining quality assurance activities within pharmaceutical manufacturing operations. The position focuses on ensuring GMP compliance, investigating deviations, driving CAPA initiatives, and supporting continuous improvement efforts. The successful candidate will work closely with production teams to enhance quality systems and maintain regulatory standards. Responsibilities -Write and manage production deviations and quality events -Monitor manufacturing processes and identify deviations from established procedures -Investigate quality issues, complaints, and non-conformances -Perform root cause analysis and develop CAPA plans -Support compliance investigations and quality improvement initiatives -Review SOPs, validation protocols, production documentation, and batch manufacturing records -Ensure compliance with GMP and company quality standards -Recommend improvements related to product quality, safety, health, and environmental standards -Participate in cross-functional quality and compliance projects -Provide quality related guidance and support to manufacturing teams -Maintain accurate documentation and reporting of quality activities Requirements -Master’s degree or…

Company Our client is a global, innovation-driven organisation operating in a highly regulated manufacturing environment. The site focuses on reliable delivery of critical products and works to high quality and compliance standards. Teams collaborate closely across Manufacturing, Quality, Engineering and Technology to improve processes and keep operations running smoothly. Job Description We are looking for a Validated Systems Engineer to strengthen the Operations Technology team in Breda. This position sits at the intersection of digital technology and the production floor, helping to improve reliability, efficiency and compliance of packaging and labelling operations. The Validated Systems Engineer will support and improve a defined set of manufacturing systems (including SCADA and system integrations), working with site stakeholders and global teams to deliver practical solutions in a GMP-regulated environment. Responsibilities – Support the design, testing, qualification and change-control of manufacturing systems in line with GMP requirements and site procedures. – Maintain and troubleshoot a portfolio of operational manufacturing systems to ensure stable day-to-day performance. – Work with cross-functional stakeholders (Manufacturing, Quality, Engineering and Technology) to identify issues, root causes and improvement opportunities. –…

Company: We are working with a leading global biopharmaceutical company dedicated to developing and manufacturing innovative medicines. Their Breda site focuses on delivering high-quality products through advanced manufacturing and technology solutions, with a strong emphasis on compliance, reliability, and continuous improvement. Job Description: The Manufacturing Systems Support Engineer plays a vital role in ensuring the reliability, efficiency, and compliance of labelling and packaging operations. This position involves working at the intersection of digital technology and manufacturing, supporting critical systems such as SCADA, automated label printing, and mobile workstations. It is an active, hands-on role suited for someone who enjoys technical problem-solving and seeing the direct impact of their work on manufacturing continuity. Responsibilities: •    Assist in the design, testing, qualification, and change management of manufacturing systems in accordance with GMP guidelines. •    Collaborate with internal teams across Breda and globally, as well as external technology partners, to identify improvement opportunities. •    Maintain, troubleshoot, and support a portfolio of manufacturing systems supporting both commercial and clinical production. •    Document processes and train staff on new technologies and systems. •    Identify recurring…