Supply Chain Specialist, Breda, Noord-Brabant

The Company A global healthcare and life sciences organization focused on pharmaceutical research, biotechnology innovation, and advanced therapeutic solutions. The company operates internationally, employing thousands of professionals dedicated to improving health outcomes through scientific research and development. Its research facilities support cutting edge work in cell therapy, gene therapy, RNA therapies, and vaccine development. Role description An experienced Environment, Health & Safety Engineer is required to support and strengthen EH&S programs within a complex research and development environment. The position focuses on improving EH&S systems, ensuring regulatory compliance, managing risk, and supporting sustainable safety performance across the organization. This role involves close collaboration with site leadership, technical experts, and operational teams to drive continuous improvement initiatives. Responsibilities - Oversee, maintain, and improve EH&S systems, processes, and practices - Lead or support implementation of EH&S standards and management systems - Coach and develop EH&S representatives, standards owners, and subject matter experts - Conduct EH&S risk assessments and recommend mitigation measures - Provide technical guidance on contractor safety, construction safety, and permit to work programs - Support EH&S evaluations for engineering and operational projects - Participate in internal and external audits, inspections, and compliance reviews - Support and verify incident investigations and corrective actions - Develop and deliver EH&S training programs - Collaborate with management and operational teams to improve site safety performance Requirements - Bachelor's degree or equivalent qualification - Minimum 5 years of experience in Environment, Health & Safety - Experience with ISO 14001 or similar international management system standards - Experience working within large, complex organizations and change management environments - Strong knowledge of regulatory compliance and safety management principles - Ability to identify systemic issues and implement sustainable solutions - Excellent communication and stakeholder management skills - Strong coaching and influencing abilities - Business oriented mindset with understanding of operational needs - Fluent Dutch and English, both written and spoken - Safety Manager Level 3, Industrial Hygiene qualification, or equivalent is advantageous Other Information If you are interested and want to apply, please submit your application via the apply button below and contact me.

Company Our client is an international manufacturing company known for operating within a highly regulated production environment. Using advanced automated manufacturing and packaging technologies, the organisation is committed to delivering high-quality products while maintaining the highest standards of safety, compliance, and operational excellence. Continuous improvement, teamwork, and innovation are key drivers of success across the site. Job Description We are currently seeking an Manufacturing Operator (GMP) to join a dynamic production team. In this position, you will be responsible for ensuring automated production lines operate efficiently, safely, and in accordance with GMP guidelines. You will play an important role in maintaining equipment performance, resolving technical issues, and supporting production continuity through proactive problem-solving and process optimisation. Key Responsibilities - Work with automated production and packaging equipment in accordance with GMP requirements and standard operating procedures. - Prepare production lines for operation by carrying out equipment set-ups, product changeovers, cleaning activities, and line clearance procedures. - Investigate and resolve equipment faults and process disruptions to minimise production downtime. - Fine-tune machine settings and process parameters to improve productivity, efficiency, and product quality. - Register and verify production information using SAP, MES, and related manufacturing systems. - Complete production documentation accurately, including batch records, equipment logs, and operational documentation. - Assist with deviation investigations and support root cause analysis using structured troubleshooting methodologies. - Collaborate with Production, Maintenance, and Quality teams to resolve technical issues and restore production performance. - Drive continuous improvement initiatives by applying Lean principles and identifying opportunities to optimise manufacturing processes. - Promote a safe working environment while ensuring effective communication during shift handovers. Requirement - Technical education at MBO level or an equivalent qualification such as VAPRO B. - Previous experience within automated production, assembly, packaging, or process manufacturing. - Strong technical aptitude with proven troubleshooting and analytical problem-solving skills. - Familiarity with structured improvement methodologies including Root Cause Analysis (RCA), 5 Why, Lean, or Kaizen. - Experience working within GMP or another regulated manufacturing environment is highly desirable. - Knowledge of SAP, Manufacturing Execution Systems (MES), or comparable production software. - Good communication skills in English. - Flexible to work rotating 3-shift and 5-shift schedules. - Available for a temporary full-time assignment via SIRE Life Sciences. Why Apply? This opportunity is ideal for someone who enjoys working with advanced manufacturing technology and takes pride in improving production performance. You'll become part of an environment where technical expertise, teamwork, and continuous improvement are valued every day. If you're looking for your next challenge in automated manufacturing, we'd love to hear from you. Apply today by clicking the application button below or contact me directly for more information.

Company: We are supporting a leading manufacturing organization committed to operational excellence and safety. Their maintenance and engineering team is responsible for managing the lifecycle of their production equipment and systems, ensuring optimal performance, safety, and compliance across their facilities. Job Description: We are seeking a highly skilled Senior Electrical Engineer to oversee the electrical systems of production equipment throughout its lifecycle. This role is vital to supporting maintenance activities, project executions, and troubleshooting efforts, ensuring the safe and efficient operation of manufacturing assets. Responsibilities: - Act as the electrical expert for production equipment, supporting engineering and modification projects, including small adjustments to existing systems and the integration of new equipment. - Provide troubleshooting support during equipment breakdowns to minimise downtime. - Oversee electrical safety standards and ensure all activities comply with Dutch regulations, including NEN 3140. - Review equipment qualifications and define roles and responsibilities for electrical safety within projects. - Collaborate with external vendors to review electrical safety aspects of machinery. - Support the planning and execution of maintenance, modifications, and upgrades, managing the entire equipment lifecycle. - Conduct and follow up on electrical safety inspections, including periodic NEN 3140/NEN-EN-IEC 60204-1 inspections, testing, and documentation. - Manage personnel appointments and qualifications within the maintenance and engineering team per NEN 3140 standards. - Provide second-line technical support for complex electrical issues faced by shopfloor technicians. - Participate in cross-functional teams for project deployment, asset upgrades, and safety improvements. - Prepare test protocols, technical evaluations, and assessment reports as required. Requirements: - Bachelor’s or master’s degree in electrical engineering or a related field. - Minimum of 7 years of relevant experience, with at least 5 years in an operational or manufacturing environment. - Proven experience as an appointed Installation Responsible Person (IV) under NEN 3140. - Strong practical knowledge of NEN-EN-IEC 60204-1 and Dutch electrical safety laws and standards. - Hands-on experience supporting production equipment and troubleshooting electrical issues. - Experience with project management, especially CAPEX projects, is advantageous. - Fluent in Dutch; good English communication skills are essential. - Strong stakeholder management and interpersonal skills. Other Information: If you are interested and want to apply, please submit your application via the apply button below and contact me. The role is fully onsite with occasional opportunities to work from home. Candidates should ideally live within approximately one hour of Breda or be willing to relocate within the Netherlands. The position may require supporting emergency breakdowns, with some work outside regular hours. 

Company Our client is an international pharmaceutical and biotechnology organization with a modern manufacturing facility in Breda. The site combines advanced production technology with strict GMP, quality, and safety standards. To support growing production activities, we are looking for several hands-on professionals who enjoy working with machinery, solving technical problems, and improving production processes.   Job Description As a Production Operations Technician, you will help ensure that manufacturing and packaging equipment performs reliably throughout the production process. You will prepare equipment for production, respond to operational issues, complete required documentation, and contribute to maintaining a safe and efficient manufacturing environment.   Responsibilities - Keep manufacturing and packaging equipment running efficiently throughout production. - Prepare machines for different production runs, including set-ups, changeovers, line clearance, and shutdown activities. - Identify equipment or process issues and carry out first-line troubleshooting. - Perform minor machine adjustments to restore or improve equipment performance. - Complete GMP and production documentation accurately and on time. - Carry out required equipment and production-area cleaning activities. - Follow established GMP, SOP, quality, and safety procedures. - Identify recurring production issues and contribute to reducing downtime and improving efficiency. - Escalate complex technical problems to the appropriate technical specialists. - Collaborate with production, quality, and technical teams to maintain smooth operations. Requirements - MBO-level education or equivalent technical/production experience. - Previous hands-on experience within manufacturing, production, packaging, or process operations. - Experience working with automated  production equipment. - Knowledge of GMP, SOPs, or regulated manufacturing procedures. - Experience completing GMP or production documentation. - Familiarity with machine set-ups, changeovers, line clearance, and close-down activities. - Experience performing cleaning activities within a production environment. - Good technical troubleshooting skills and confidence making minor equipment adjustments. - Good communication skills in English. - Willingness to work within a rotating shift schedule. Interested? If you enjoy hands-on technical work, modern production technology, and problem-solving, we would like to hear from you.  

Company A leading global biotechnology organization dedicated to discovering, developing, and delivering innovative medicines for patients with serious illnesses. Driven by science and powered by advanced technology, the organization focuses on areas such as oncology, cardiovascular disease, inflammation, and rare diseases. Its mission is centered on improving lives by turning cutting-edge science into meaningful therapies that address unmet medical needs.   Job Description As a Senior Electrical Engineer you will support maintenance, engineering, and project activities within a modern manufacturing environment. You will act as the electrical expert, lead electrical safety initiatives, support equipment upgrades, and contribute to the successful delivery of capital projects.   Responsibilities Provide electrical expertise to maintenance and project teams. Act as Installation Responsible Person (IV) and oversee electrical safety compliance. Support new equipment installations, upgrades, and CAPEX projects. Manage electrical inspections in line with NEN 3140 and NEN-EN-IEC 60204-1. Review electrical modifications and ensure compliance with safety and quality standards. Troubleshoot complex electrical and equipment-related issues. Develop test protocols, technical assessments, and engineering documentation. Collaborate with cross-functional teams including Engineering, Automation, QA, Validation, Manufacturing, and Supply Chain.   Requirements Bachelor’s or Master’s degree in Electrical Engineering or a related field. 7+ years of relevant experience, including 5+ years in manufacturing or operations. Strong knowledge of industrial electrical systems and Dutch electrical safety regulations. Experience as an appointed IV under NEN 3140. Experience in project engineering and CAPEX projects. GMP or other regulated industry experience is preferred. Fluent in English and Dutch. Strong communication, stakeholder management, and problem-solving skills. Other Information Apply to our vacancy for more information. Looking forward to getting in touch!

Company  Our client is a global leader in dairy and plant-based ingredients, serving professional customers such as bakeries, fast-food outlets, hotels, restaurants, catering services, and industrial food and beverage companies. They are committed to delivering high-quality, innovative solutions through extensive market knowledge and operational excellence. Job Description We are seeking an experienced Supply Planning Team Leader to oversee the European Material Planning team. This role involves leading a team responsible for ensuring the timely procurement of raw materials and packaging supplies to support production across multiple locations. The ideal candidate will focus on optimizing inventory, managing supplier relationships, and supporting tactical planning to meet production and supply chain objectives. Responsibilities - Lead and manage the European Material Planning team, comprising three team members. - Oversee the end-to-end ordering process for raw and packaging materials. - Monitor inventory levels and optimize working capital. - Forecast material requirements based on production schedules and adjust plans accordingly. - Resolve supplier issues and manage purchase complaints. - Ensure accurate processing of orders and invoices. - Develop and support the team, and manage KPIs such as supplier OTIF and inventory value. - Collaborate with suppliers on tactical alignment, contract coverage, and contingency planning. - Drive continuous improvement initiatives within the supply planning process. - Support long-term planning and strategic alignment with procurement teams. - Facilitate regular team check-ins and performance reviews, providing coaching and escalation support. - Coordinate with production locations in the Netherlands and Germany, including weekly travel to Meppel and periodic visits to Lippstadt. Requirements - HBO/Bachelor’s degree in Supply Chain, Logistics, or a related field. - Preferably 1+ year of leadership experience in supply planning or ERP planning. - Strong knowledge of supply chain and production processes. - Proficiency in SAP. - Fluency in Dutch and English; German language skills are a plus. - Excellent communication and stakeholder management skills. - Ability to oversee complex operations, escalate issues when necessary, and look beyond daily tasks to strategic horizons. - Proactive, team-oriented, and customer-focused with a drive for operational excellence. - Willing to travel regularly to Meppel and occasional trips to Lippstadt. Other Information This is a temporary position initially lasting around six months, with the possibility of extension. The role involves flexible working, with hybrid options (office in Amersfoort, with weekly travel to Meppel). The candidate should be comfortable managing a team that operates independently and interacting with various departments and suppliers.  If you are interested and want to apply, please submit your application via the apply button below and contact me.

The Company The client is one of the Netherlands’ biggest dairy products manufacturers who is also active globally.    Role Description As the MRP Lead you will lead a team of three Material Requirements Planning (MRP) professionals responsible for ensuring the timely availability of raw materials and packaging components for production sites in Meppel and Lippstadt. The role combines people leadership, supply planning expertise, supplier management, and tactical supply chain oversight. You will be part of the Encaps Supply Team, a global leader in dairy and plant-based ingredient solutions. In this position, you will ensure optimal material availability, support business continuity, drive supplier performance, and contribute to achieving the right balance between cost, service, and inventory levels. The role requires both operational involvement and a tactical outlook, partnering closely with suppliers, procurement, production, and other key stakeholders. Responsibilities Lead and coach a team of three Material Planners. Support team members in managing priorities, resolving issues, and handling escalations. Facilitate regular team check-ins and performance discussions. Foster professional growth and continuous development within the team. Oversee the end-to-end planning and ordering process for raw materials and packaging materials. Ensure material availability to support uninterrupted production and delivery performance. Adjust planning activities in response to changing production schedules and demand requirements. Forecast material requirements based on supply and production plans. Monitor and optimize inventory levels while balancing working capital and service performance. Build and maintain strong relationships with suppliers and internal stakeholders. Conduct tactical supplier performance reviews and drive continuous improvements. Manage supplier escalations and support resolution of supply-related issues. Collaborate with Procurement on long-term volume planning, contract coverage, and supply continuity strategies. Develop contingency plans and alternative sourcing options to mitigate supply risks. Own and monitor key MRP performance indicators, including Supplier OTIF and Raw & Packaging Inventory Value. Identify opportunities to improve planning processes, supplier performance, and operational efficiency. Challenge existing ways of working and implement sustainable improvements. Contribute to strategic and tactical supply chain initiatives beyond day-to-day operations. Requirements Bachelor's degree (HBO/University level) in Supply Chain Management, Logistics, Business Administration, or a related field. Experience in Supply Planning, Material Planning, ERP Planning, or a similar supply chain role. Previous leadership or team coordination experience is preferred, ideally around one year or more. Knowledge of manufacturing and supply chain processes. Strong SAP proficiency. Good understanding of inventory management, material planning, and supplier performance management. Experience working in complex, fast-paced production environments. Strong communication and stakeholder management skills. Proactive, hands-on, and solution-oriented mindset. Ability to escalate issues effectively and manage supply risks in a Just-in-Time (JIT) environment. Customer-focused with a strong drive for operational excellence. Commercially aware with a clear understanding of cost and working capital impacts. Continuous improvement mindset with the confidence to challenge the status quo. Strong team player capable of operating across multiple stakeholders and functions. Able to balance operational execution with tactical and longer-term planning horizons. Fluent in Dutch and English. German language skills are considered an advantage. Willingness to travel regularly to Meppel (approximately once per week) and occasionally to Lippstadt (approximately once every 1-2 months). Based primarily in Amersfoort with a hybrid working arrangement. Other Information Apply to our vacancy for more information. Looking forward to getting in touch! 

Company: Our client is a leading organization in the pharmaceutical industry, dedicated to ensuring the highest standards of product quality and compliance. They operate within a heavily regulated environment, committed to delivering safe and effective medicines to the market. Job Description: We are seeking an experienced Quality Assurance Specialist to oversee the release of pharmaceutical products, ensuring all are compliant with applicable laws, regulations, and internal standards. This key role involves inspecting, reviewing, and authorizing product documentation, managing quality investigations, and supporting regulatory inspections. Responsibilities: •    Review and approve master documents and specifications to support product release. •    Initiate and evaluate quality investigations, including deviations, to determine release or rejection, and implement improvement proposals. •    Ensure timely completion of deviation and investigation reports. •    Lead quality improvement initiatives to control production risks. •    Authorize ongoing stability studies and Product Quality Reviews. •    Prepare for and oversee inspections by government agencies and customers. •    Participate in self-inspections across production, laboratory, storage, and distribution areas. •    Support and coordinate handling of complaints, root cause analysis, and implementation of corrective actions. •    Manage product recalls and stock blockage proposals. •    Investigate and document deviations and complaints thoroughly. •    Develop and maintain relationships with external partners related to quality oversight. •    Participate in technology transfer activities and contribute to process improvements. •    Provide functional leadership to QA team members, including organizing work, implementing structured procedures, and contributing to staffing and training decisions. Requirements: •    Degree in pharmacy, chemistry, biology, or a related field (per EU Directive 2001/83/EC). •    Extensive experience with aseptic manufacturing processes (preferably over 5 years). •    Knowledge of lyophilization and visual inspection processes is a plus. •    Familiarity with automated pharmaceutical processes. •    Strong understanding of EU and US pharmaceutical laws and regulations. •    Proficient in analytical methods. Other Information: If you are interested and want to apply, please submit your application via the apply button below and contact me.

Company  Our client is a well-established, international food production and ingredients organisation with multiple manufacturing sites in Europe. They operate in a fast-paced supply chain environment where service, quality, and continuity of production are critical. The culture is professional, collaborative, and focused on continuous improvement. Job Description  For our client, we are looking for a Materials Planner to lead a small European materials planning team and ensure the timely availability of raw and packaging materials for production. The Materials Planning Team Lead (SAP) balances day-to-day operational priorities with a more tactical, forward-looking approach, working closely with internal stakeholders and suppliers to protect supply continuity. Responsibilities  - Lead and support a small materials planning team responsible for raw and packaging material availability across multiple production sites. - Manage the end-to-end ordering process for materials, ensuring orders are placed accurately and on time. - Monitor and optimise inventory levels while supporting working capital targets. - Translate production plans into material requirements and adjust plans when schedules change. - Coordinate and resolve supplier-related issues, including delivery problems and purchase complaints. - Ensure accurate order handling and invoice control in collaboration with relevant internal teams. - Drive performance management for the materials planning scope, including supplier delivery performance (e.g., OTIF) and inventory value. - Prepare and run structured supplier performance reviews and align on improvement actions. - Build and maintain contingency approaches to reduce risk and improve supply reliability. - Support escalations when supply risks impact production, and align actions with key stakeholders. - Identify improvement opportunities and take ownership for implementing practical solutions. Requirements  - Bachelor-level education (Supply Chain, Logistics, or a related field). - Strong experience in materials planning / supply planning / ERP planning. - Proven ability to lead, guide, or coach a team (formal people leadership is a plus). - Solid SAP proficiency (required). - Fluent in Dutch and English (German is a plus). - Strong communication skills and confident stakeholder management. - Proactive, improvement-minded, and able to challenge the status quo constructively. - Willingness to travel regularly to a Dutch production site and occasionally to a German site. - Temporary Full-Time Contract (6 Months) Other Information The role is based in the Netherlands with a mix of on-site and hybrid working, depending on business needs. Regular interaction with production, procurement, and suppliers is key, and the successful candidate will be comfortable operating in a time-sensitive supply environment. If you are interested and want to apply, please submit your application via the apply button below and contact me.

The Company A global pharmaceutical organization focused on science driven innovation, technology excellence, and high quality manufacturing. The company operates across international markets and collaborates closely with manufacturing sites, technical operations teams, and external manufacturing partners to deliver compliant and efficient product supply. Role description The Technology Transfer Program Manager is responsible for leading Small Molecule drug product technology transfer projects across manufacturing sites. The role provides end to end oversight of transfer execution, ensuring projects are delivered on time, within quality standards, and in compliance with GMP and regulatory requirements. This position works closely with internal stakeholders, manufacturing facilities, contract manufacturing organizations, and global teams to drive successful technology transfer outcomes while continuously improving transfer methodologies and governance processes. Responsibilities - Lead and coordinate multiple Small Molecule technology transfer projects simultaneously - Manage site to site transfer execution activities across manufacturing networks - Monitor project timelines, milestones, risks, and project performance metrics - Ensure transfers are completed according to quality, compliance, and regulatory requirements - Coordinate activities between donor and receiving manufacturing sites - Collaborate with Manufacturing, Quality, Regulatory, Supply Chain, Procurement, Finance, PTS, and ATS teams - Facilitate stakeholder alignment on project objectives and deliverables - Act as the primary point of contact for technology transfer activities - Develop and maintain governance frameworks and project reporting structures - Coach project teams and support transfer sponsors throughout project execution - Support regulatory submission activities related to technology transfers - Assist with process validation, qualification, and technical documentation - Drive continuous improvement initiatives and technology transfer best practices - Provide expertise in technical problem solving and issue resolution Requirements - Bachelor of Science degree in Engineering, Chemistry, Biology, or a related scientific discipline - More than 10 years of experience in Technology Transfer, Product Development, Manufacturing Operations, or Technical Operations - Strong experience with Small Molecule pharmaceutical products - Knowledge of liquids, ointments, creams, sterile injectables, sterile pastes, and powder filling processes - Strong understanding of EU and FDA GMP regulations - Experience with change control, deviation management, technical protocols, and technical reports - Experience with regulatory licensing documentation - Expert level project management and project controlling skills - Advanced stakeholder management and communication skills - Experience working within complex matrix organizations - Ability to lead cross functional teams without direct authority - Strong negotiation and influencing capabilities - Experience using Microsoft Project and enterprise project management tools - Fluent English communication skills - Experience working with multicultural and geographically diverse teams - Knowledge of German or French is an advantage Other Information If you are interested and want to apply, please submit your application via the apply button below and contact me