Supply chain Coordinator, Breda, Noord-Brabant

The Company A global organization operating within the pharmaceutical and life sciences sector, focused on developing and manufacturing innovative therapies for patients worldwide. The company operates in a highly regulated environment and is committed to digital transformation, quality excellence, and continuous process improvement across laboratory operations. About the Role We are seeking an experienced Paperless Lab Design Lead to support the deployment, optimization, and maintenance of digital laboratory systems within an Advanced Therapies Quality Control environment in Leiden, Netherlands. This role serves as the subject matter expert for paperless laboratory initiatives, driving method digitalization, standardization, and harmonization while working closely with laboratory SMEs, quality teams, and system stakeholders. Responsibilities -Drive harmonization activities and convert paper based laboratory methods into digital workflows -Create, configure, and maintain method execution templates within the LIMS platform -Support change control impact assessments when required -Contribute to the design and management of master data used in digital laboratory methods -Coordinate master data validation activities -Create and update technical documentation following standardization processes -Manage enhancements and modifications to existing digital methods -Deliver training and support to laboratory personnel on newly deployed digital methods -Serve as the primary contact for laboratory system related questions -Assist with setup, testing, and validation of LIMS instrument interfaces Requirements -Bachelor’s degree in chemical sciences, Life Sciences, or a related scientific discipline -Advanced degree preferred -Minimum 5 years of experience in Quality Assurance, Quality Control, Analytical Testing, IT, or related    functions -Experience in pharmaceutical manufacturing, advanced therapies, or another highly regulated industry -Knowledge of laboratory testing techniques is preferred -Hands on experience with LIMS platforms, preferably Lab Vantage -Experience as a key user, business administrator, or system owner for digital laboratory systems -Understanding laboratory instrument integration with LIMS is an advantage -Experience participating in process improvement projects -Strong communication, stakeholder management, and presentation skills Other Information If you are interested and want to apply, please submit your application via the apply button below and contact me.  

The company Our client is a leading international organisation operating in a highly regulated food and consumer products environment. The organisation has a strong focus on innovation, product safety, sustainability, and the development of packaging solutions for global markets. As part of the global packaging development function, you will work in an international and multidisciplinary environment, collaborating with teams across Research & Development, Regulatory Affairs, Quality Assurance, Procurement, and Supplier Quality Management. Role Description As a Packaging Regulatory & Compliance Specialist, you will be responsible for assessing packaging materials and ensuring compliance with applicable food-contact, packaging, and product safety regulations across international markets. You will provide regulatory and technical advice to internal stakeholders and external customers, review and manage packaging compliance documentation, and support the implementation of new regulatory requirements. The role offers the opportunity to contribute to packaging development projects, sustainability initiatives, and global compliance activities. Responsibilities • Review, assess, and finalise packaging compliance documentation, ensuring alignment with internal standards and applicable regulatory requirements. • Assess packaging materials for food-contact and regulatory compliance across different international markets. • Draft, review, and manage compliance documentation, including Declarations of Compliance and related supporting documentation. • Assess packaging requirements related to PFAS, heavy metals, and other relevant chemical and material compliance standards. • Verify that packaging materials meet applicable local and international regulations in the markets where products are sold. • Advise and support cross-functional stakeholders on packaging compliance, food-contact materials, and regulatory requirements. • Support the resolution of packaging compliance challenges within product and packaging development projects. • Respond to food safety and packaging compliance questions from internal stakeholders and external customers. • Maintain accurate packaging compliance data, specifications, and documentation within relevant systems. • Support the assessment and implementation of Packaging and Packaging Waste Regulation (PPWR) requirements, including compliance checks and related projects. • Collaborate with Regulatory Affairs, Quality, Procurement, Supplier Quality, R&D, and other international teams to ensure effective compliance management. • Participate in regular compliance team meetings and contribute to continuous improvement of packaging compliance processes and standards. Requirement • Bachelor's or Master's degree in Material Science, Chemistry, Packaging, Food Science, Food Technology, or a related discipline. • Approximately 5–7 years of relevant professional experience in packaging compliance, regulatory affairs, technical compliance, food-contact materials, or a similar field. • Strong experience with European packaging and food-contact compliance regulations. • Experience working with packaging materials in the food, food ingredients, food chemicals, or another highly regulated industry. • Knowledge of packaging and food-contact regulations, compliance assessments, and regulatory risk evaluation. • Experience with compliance documentation, including Declarations of Compliance, is highly relevant. • Familiarity with Packaging and Packaging Waste Regulation (PPWR) and related requirements. • Experience with specification management systems; knowledge of SAP PLM is an advantage. • Strong analytical skills with a high level of accuracy and attention to detail. • Proactive, hands-on approach with a strong sense of ownership and willingness to develop new knowledge and processes. • Excellent communication and presentation skills, with the ability to work effectively with both technical and non-technical stakeholders. • Comfortable working in international, cross-functional teams. • Fluent in English; knowledge of Dutch is not required. Other information Looking for a new opportunity in packaging compliance and regulatory affairs? This could be your next challenge! If you're interested, please click the below button to apply for the job.

Company Our client is a global, innovation-driven organisation in the food sector with an international R&D environment. The team works on developing and improving packaging materials and formats for diverse markets worldwide, with a strong focus on product quality, consumer safety, and compliance with evolving regulations. Job Description We are looking for a Packaging Compliance Specialist to support a global packaging team by ensuring packaging materials meet internal standards and regulatory requirements. The focus of this role is to review and finalise compliance documentation, advise stakeholders on food contact compliance topics, and help keep global compliance data accurate and up to date. Responsibilities - Review, assess, and finalise packaging compliance documentation in line with internal requirements and applicable regulations. - Evaluate packaging materials for compliance topics such as food contact requirements and market-specific rules. - Prepare, review, and manage compliance documentation, including Declarations of Compliance. - Support cross-functional stakeholders (e.g., Regulatory Affairs, Quality, Procurement, Supplier Quality) with compliance guidance during development projects. - Respond to packaging compliance and food safety-related questions from internal stakeholders and external customers. - Maintain and improve packaging compliance data and documentation to ensure accuracy and traceability. - Support the assessment and implementation of packaging regulatory changes (including Packaging and Packaging Waste Regulation-related requirements). - Participate in regular team meetings and contribute to continuous improvement of compliance processes. Requirements - Bachelor’s or Master’s degree in Material Science, Chemistry, Packaging, Food Science/Technology, or a related field. - Several years of relevant experience in food contact material regulation and packaging compliance. - Strong understanding of European packaging and food contact regulations and practical experience applying them. - Accurate, analytical, and proactive working style with strong ownership and attention to detail. - Strong communication and stakeholder management skills in an international environment. - Fluency in English. - Experience with specification management systems (preferably SAP PLM) is a plus. -Temporary Full-Time Contract (4 Months) Other Information The selection process typically includes an online interview. If you are interested and want to apply, please submit your application via the apply button below and contact me.

About the Company Join a global healthcare organization at a state-of-the-art manufacturing site in Leiden. As part of the Facilities team, you will play a key role in ensuring the reliability, safety, and compliance of facility infrastructure, utilities, and manufacturing support systems within a highly regulated GMP environment. Role Description As a Facilities Engineer, you will oversee the operation, maintenance, and continuous improvement of building services, utilities, and facility systems. Working closely with Engineering, Maintenance, EHS, Quality, and external contractors, you will ensure equipment reliability, regulatory compliance, and operational excellence while supporting site improvement projects. Key Responsibilities Coordinate the maintenance and operation of facility systems, utilities, and building infrastructure Ensure compliance with GMP, GxP, EHS, and quality standards Lead equipment reliability and preventive maintenance initiatives Support facility upgrades, maintenance projects, and infrastructure improvements Supervise contractors and monitor service quality, budgets, and project progress Identify operational risks and implement mitigation actions Drive continuous improvement initiatives focused on safety, reliability, and efficiency Support CAPA implementation, change controls, and regulatory compliance activities Monitor energy usage and contribute to sustainability and cost-saving initiatives Collaborate with cross-functional teams to support manufacturing operations Requirements 5+ years of experience in Facilities Engineering, Maintenance, or Technical Operations Experience within a GMP-regulated manufacturing environment (pharmaceutical, biotechnology, medical devices, or similar) Strong knowledge of facility utilities, maintenance systems, and infrastructure Experience with preventive maintenance, contractor management, and project coordination Good understanding of EHS, Quality Management Systems, and CAPA processes Strong troubleshooting and problem-solving skills Excellent communication and stakeholder management abilities Fluent in English

Company A leading financial institution in the Netherlands, operating in a highly regulated and complex environment. They invest heavily in building secure, resilient, and modern technology platforms to support critical banking services. Job Description We are seeking a Platform Services Architect to shape the future of the organization’s platform architecture. This role involves translating business needs, regulatory standards, and technology developments into clear, practical solutions. The focus is on designing and improving platform services across operating systems, storage, backup, disaster recovery, and cyber resilience, ensuring the infrastructure remains secure, scalable, and reliable. Responsibilities -Develop and maintain the architecture blueprint for platform services, ensuring it aligns with business goals and regulatory requirements. -Guide architectural decisions related to Linux, Windows, storage, backup, and recovery solutions. -Shape strategies for disaster recovery, cyber resilience, and data protection, balancing security and operational efficiency. -Collaborate closely with Solution Architects and cross-functional teams to ensure architectural -consistency and best practices. -Lead the development of technical roadmaps and communicate architectural vision to stakeholders across the organization. -Act as a trusted advisor for engineering, security, and senior management on complex infrastructure challenges. -Identify opportunities to standardize, improve, and modernize platform services for better efficiency and security. -Co-lead the Platform Services area alongside senior leaders and provide guidance to technical teams. Requirements -Master’s degree or equivalent professional experience in a relevant field. -Extensive experience working in complex IT infrastructure environments, with a focus on enterprise architecture. -Strong knowledge of Linux and Windows operating systems. -Deep understanding of storage, backup, disaster recovery, and cyber security strategies. -Experience with on-premise, cloud, and hybrid infrastructure environments. -Ability to communicate complex technical concepts effectively to both technical and non-technical audiences. -Experience working across multiple teams and stakeholders. -Collaborative and pragmatic approach to architecture and problem-solving. -Fluency in English and Dutch is essential. -Experience within regulated sectors, like financial services, is highly advantageous. Other Information If you are interested and want to apply, please submit your application via the apply button below and contact me.  

Location : Breda, North Brabant, Netherlands (On-site) / 3-5 Shift pattern About the Company Our client is a global biotechnology company dedicated to improving the lives of patients through innovative medicines. Their Breda site is an international manufacturing and supply chain hub where products are packaged, labeled, assembled, and prepared for distribution to patients around the world. Working in a modern GMP-regulated production environment, you'll become part of a diverse team focused on quality, safety, continuous improvement, and operational excellence. Whether you're starting your manufacturing career or already have extensive technical experience, there are opportunities to grow and develop within the organization. About the Role We are recruiting Production / Technical Operator for the manufacturing team in Breda. Depending on your experience and technical background, you will work on manual, semi-automated, or fully automated production lines. You'll help ensure production runs safely, efficiently, and according to strict quality standards. Some positions focus primarily on manual packaging and production activities, while others involve operating equipment, troubleshooting technical issues, and improving production processes. Responsibilities   Execute production and packaging activities according to established procedures. Prepare production lines, perform set-ups, changeovers, and cleaning activities. Supply materials and support smooth production flow. Monitor product quality and report deviations when necessary. Complete production documentation accurately and in compliance with GMP requirements. Operate and monitor production equipment, depending on the role. Troubleshoot production issues and support continuous improvement initiatives where applicable. Maintain a safe, clean, and organized working environment. Collaborate closely with colleagues from production, maintenance, and quality departments. Qualifications   Experience in a production, manufacturing, logistics, packaging, or technical environment. Good command of English. Comfortable working according to procedures and quality standards. Reliable, accurate, and safety-conscious with strong attention to detail. Willingness to work in a shift system (2, 3, and 5 shifts). Technical affinity is an advantage for operators working with automated production lines. Experience in a GMP or other highly regulated environment is beneficial but not essential. Candidates from industries such as food, automotive, electronics, or high-tech manufacturing are also encouraged to apply if they have strong technical skills and a structured way of working. Required Skills   Experience in a production, manufacturing, logistics, packaging, or technical environment. Good command of English. Comfortable working according to procedures and quality standards. Reliable, accurate, and safety-conscious with strong attention to detail. Willingness to work in a shift system (2, 3, and 5 shifts). Technical affinity is an advantage for operators working with automated production lines. Preferred Skills   Experience in a GMP or other highly regulated environment is beneficial but not essential. Candidates from industries such as food, automotive, electronics, or high-tech manufacturing are also encouraged to apply if they have strong technical skills and a structured way of working.

The company Our client is a global biopharmaceutical organisation committed to advancing innovative medicines that improve patients' lives worldwide. Through advanced research, biologics manufacturing, and a strong focus on quality and innovation, the organisation delivers life-changing therapies across a wide range of therapeutic areas. Role Description As a LIMS Specialist, you will play a key role in the implementation, maintenance, and digitalisation of laboratory methods within a regulated Quality Control environment. You will focus on LIMS method templates, master data, validation, and the harmonisation of paper-based laboratory methods into digital workflows. You will also support laboratory teams with digital processes, instrument interfaces, and LIMS-related activities. Responsibilities - Lead the harmonisation and digitalisation of paper-based laboratory methods within a regulated QC environment. - Create, configure, and maintain method execution templates, master data, and digital laboratory methods in LIMS. - Support validation activities, change controls, and technical documentation related to digital laboratory processes. - Manage updates and improvements to existing digital methods in collaboration with laboratory SMEs and other sites. - Support the setup, testing, and validation of LIMS-to-instrument interfaces and related digital laboratory workflows. - Act as a key point of contact for laboratory users regarding LIMS, digital methods, and laboratory workflows. - Provide training and guidance to laboratory teams on digital methods and LIMS functionality. - Collaborate with laboratory, Quality, IT, and technical stakeholders to ensure effective implementation and maintenance of digital laboratory solutions. Requirement - Bachelor's degree or equivalent qualification in Chemical Sciences, Life Sciences, or a related field. - Minimum 5 years of experience in Quality Control, Quality Assurance, analytical testing, laboratory systems, or IT within a regulated environment. - Hands-on experience working with LIMS; experience with LabVantage is highly desirable. - Experience as a LIMS Key User, Business Administrator, Subject Matter Expert, or in a similar role is preferred. - Good knowledge of GMP/GxP requirements, laboratory testing, validation, and change-control processes. -  Strong communication and stakeholder-management skills. - Ability to work effectively with both laboratory and technical teams in a regulated environment. - Structured and analytical approach with strong attention to detail. Other information Looking for a new opportunity? Well, it's right here! If you're interested, please click the below button to apply for the job.

The Company A leading international industrial manufacturing organization with large scale operations and a strong focus on operational excellence, asset reliability, and procurement governance. The organization is currently investing in enhanced financial control, contract compliance, and risk management initiatives to strengthen transparency and ensure proper application of supplier agreements and payment processes. Role description We are seeking an experienced Procurement Specialist to join a temporary Spend Validation Team focused on reviewing and validating supplier related transactions and contract compliance activities. In this role, you will assess high value and complex Service Entry Sheet transactions, investigate commercial and contractual deviations, identify financial risks, and provide fact based recommendations. You will work closely with Procurement, Finance, Operations, Contract Management, suppliers, and senior stakeholders. Responsibilities - Review and validate Service Entry Sheet transactions against contractual agreements - Verify rates, quantities, materials, surcharges, and completed work - Analyze supporting documentation and evidence for transaction approval Investigate discrepancies, compliance concerns, and financial leakage risks - Interpret supplier contracts and assess correct commercial application - Communicate with suppliers, contract owners, operational teams, and stakeholders - Support reviewers on complex contractual and commercial cases - Escalate high risk findings to senior specialists and leadership teams - Document findings and provide evidence based conclusions - Contribute to process improvement initiatives and spend control measures - Assist with reporting, analysis, and risk management activities - Support a transparent and controlled payment process Requirements - HBO degree in Purchasing, Business Administration, Supply Chain Management, - - Finance, Commercial Economics, or a related field - Minimum 4 years of relevant experience - Experience in procurement, supplier management, contract management, or commercial controls - Strong contract interpretation and analytical skills - Experience reviewing financial, commercial, or contractual documentation - Strong risk awareness and control mindset - Ability to independently assess complex situations and make informed decisions - Strong stakeholder management and communication skills - Experience in industrial or technical environments is advantageous - Knowledge of SAP is preferred - Experience with Service Entry Sheet processes is highly desirable - Experience with compliance, audit, assurance, or control environments is advantageous - Fluent in Dutch and English - NEVI certifications are considered an advantage Other Information If you are interested and want to apply, please submit your application via the apply button below and contact me.

About the Company An international biotechnology organization active in cell therapy for oncology treatments. The company operates a highly regulated GMP manufacturing facility in Hoofddorp, closely connected to global hospital networks to process patient-derived cellular products for clinical and commercial use. Role Description As a Haematology Therapy Manufacturing Specialist, you will support the manufacturing of autologous cell therapy products in a GMP cleanroom environment. After completing the initial training program, you will be assigned to either the Production Team (PT) or the Production Support Team (PST). This is a hands-on, operational role with a strong focus on aseptic processing, documentation accuracy, and compliance. The position follows a two-shift system, including weekends, and requires working in full gowning within Grade A/B/C cleanroom environments. Key Responsibilities Production Support Team (PST) Perform apheresis material accessioning and transfer to manufacturing areas Prepare growth media in Grade C cleanroom environments Supply manufacturing suites with required materials and components Perform material decontamination prior to cleanroom entry Manage batch documentation flow to and from cleanroom nests Support batch record review to ensure timely release Perform visual inspection of final product Cryopreserve excess cells and final product Transfer and submit samples to QC for testing Production Team (PT) Execute clinical and commercial manufacturing steps in Grade A/B cleanrooms according to batch records and SOPs Support GMP runs in collaboration with PST, Product Sciences, QA, QC, and Material Management Draft and revise batch records, SOPs, and work instructions Support deviation investigations and change management activities Troubleshoot process- and equipment-related issues Ensure strict compliance with cGMP requirements and accurate documentation Maintain cleanroom nests in an optimal state Identify opportunities for process improvements to enhance quality and efficiency Working Conditions Two-shift system: Morning: 07:00 – 15:00 Evening: 16:30 – 23:30 / 00:00 Weekend shifts included On-site role Full cleanroom gowning required Training period of approximately 2 months (day shift) Working with blood-derived biological materials (hepatitis B vaccination recommended) Requirements Vocational / technical education (MBO level or equivalent); maximum completed level: BSc Experience in a GMP-regulated manufacturing environment (biotech, pharma, medical devices) Knowledge of pharmaceutical or biotechnology manufacturing processes Comfortable working in aseptic cleanroom environments Strong attention to detail and ability to strictly follow SOPs Willingness to work shift schedules, including weekends Professional working proficiency in English

The Company Our client is one of the Netherlands’ leading financial institutions, with a strong presence in banking and a large-scale technology environment supporting critical financial services. The organisation is committed to innovation, security and resilience, continuously investing in modern technology platforms and secure digital solutions. Job Description As a Platform Architect, you will shape the architecture and roadmap for critical IT platform services across Linux, Windows, storage, backup, disaster recovery and cyber resilience. You will work closely with Engineering, Security and senior stakeholders, guiding Solution Architects and translating business, security and regulatory requirements into scalable, secure and resilient technology solutions. Responsibilities Develop and maintain the architecture blueprint for Platform Services, including operating systems, storage, backup, disaster recovery, and cyber resilience. Collaborate with stakeholders to translate business needs and regulatory demands into detailed technical strategies. Provide architectural guidance on Linux, Windows, SAN, NAS, object storage, and archiving solutions. Lead the design of backup, restore, disaster recovery, and cyber recovery strategies, balancing security, operational complexity, and costs. Co-lead the Platform Services area alongside the Area Lead and Tech Lead, providing strategic direction. Support Solution Architects across multiple teams, ensuring alignment with enterprise standards and regulations. Develop roadmaps and communicate technical strategies effectively to both technical and senior business stakeholders. Facilitate cross-team collaboration and promote best practices for platform standardisation, modernisation, and improvement. Requirements Master’s degree or equivalent professional experience in a relevant field. Extensive experience in complex IT infrastructure and architecture, especially within regulated environments. Proven track record in Business, Enterprise, Solution, or Platform Architecture. Strong expertise in Linux and Windows environments. Deep knowledge of storage solutions, backup & restore, disaster recovery, and cyber resilience. Experience with both on-premise and hybrid cloud infrastructures. Ability to communicate technical concepts clearly to diverse audiences, including non-technical stakeholders. Proven experience working across multiple teams and disciplines collaboratively. Fluency in English and Dutch is essential. Other Information Apply to our vacancy for more information. We look forward to hearing from you!