Co-Packing Operations Coordinator, Rijswijk, Zuid-Holland

Company A leading international organization in the life sciences sector is strengthening its regional distribution capabilities. The company operates in a highly regulated environment and works closely with external logistics and distribution partners to ensure product availability, quality, and compliance across multiple countries. Job Description For our client, we are looking for a Supply Chain Operations Manager to ensure reliable, compliant supply while managing logistics partners and improving end-to-end cold chain distribution solutions. The role focuses on service performance, supplier management, continuous improvement, and cross-functional project work across the region. Responsibilities Ensure supply continuity, service level performance, and cost control in a GDP-compliant environment. Develop, select, and implement cold chain distribution solutions within the regional supply chain. Lead regular performance and business reviews with logistics and supply chain partners, covering escalations, reporting, and improvement actions. Maintain strong relationships with third-party partners and support internal stakeholders when issues need to be escalated. Manage and maintain agreements with supply chain partners, including driving improvements in quality, performance, and compliance. Identify and deliver continuous improvement initiatives, including savings and operational efficiency opportunities. Monitor emerging trends and legislative changes that could impact distribution solutions or cold chain practices, and assess implications proactively. Build strong internal stakeholder networks (affiliates and corporate functions) and contribute to regional projects and key initiatives. Plan, build, and manage distribution lanes for the region to support strategic priorities. Requirements Master’s degree (or equivalent) in Supply Chain / Logistics, Industrial Engineering, Change Management, or similar. Strong experience in logistics and supplier/partner management (including process improvement). Solid knowledge of supply chain, cold chain, and warehousing. Proven project management experience across departments and geographies. Strong analytical skills (including Excel) with the ability to turn data into clear insights. Fluent in English (written and spoken). Self-starter who can work independently, handle pressure, and collaborate effectively. Strong stakeholder management, negotiation, and communication skills. Preferred: knowledge of GMP/GDP, Operational Excellence tools (e.g., Six Sigma, FMEA), and experience with SAP/BW and service level agreements. Other Information This position offers the opportunity to work in an international, regulated environment where cold chain performance, compliance, and supplier collaboration are critical to success. The successful candidate will play a key role in strengthening distribution performance and driving improvements across the region. If you are interested and want to apply, please submit your application via the apply button below and contact me.

Company: A leading manufacturing organization committed to delivering high-quality products and maintaining excellence in operational safety and efficiency. The company operates a modern, innovative environment with a focus on continuous improvement and employee development. Job Description: We are seeking an experienced Senior Electrical Equipment Engineer to oversee the electrical aspects of production equipment throughout its lifecycle. This key role involves supporting engineering projects, ensuring electrical safety, and providing troubleshooting support within a manufacturing setting. Responsibilities: •    Support and lead modifications and upgrades of existing production equipment and assist with the integration of new machinery. •    Provide expert advice on electrical safety and compliance in line with Dutch regulations and standards. •    Act as the primary electrical subject-matter expert for the production process, working closely with external vendors and internal teams. •    Perform equipment qualification reviews and manage electrical safety inspections, including periodic NEN 3140/NEN-EN-IEC 60204-1 checks. •    Support troubleshooting and emergency repairs on production lines. •    Review electrical modifications and ensure adherence to safety standards, GMP, and quality requirements. •    Manage electrical safety documentation, inspections, and personnel appointments in accordance with NEN 3140. •    Assist in developing test protocols, technical evaluations, and assessment reports for electrical systems. •    Collaborate cross-functionally with project teams, maintenance technicians, vendors, and other stakeholders to ensure optimal performance and safety of electrical equipment. Requirements: •    Bachelor’s or master’s degree in electrical engineering or a related field. •    At least 7 years of relevant experience, including 5+ years in a manufacturing or production environment. •    Proven experience as an Installation Responsible Person (IV) under NEN 3140. •    Strong practical knowledge of Dutch electrical safety laws and standards, including NEN 3140 and IEC 60204-1. •    Extensive hands-on experience with electrical safety, troubleshooting, and equipment lifecycle management. •    Excellent communication skills in Dutch (native or proficient) and English. •    Ability to work independently and manage multiple projects simultaneously. Other Information: If you are interested and want to apply, please submit your application via the apply button below and contact me.

Company Overview Our client is a leading innovator in health technology, dedicated to developing advanced medical solutions that enhance patient care and improve health outcomes. They operate globally, integrating cutting-edge research and development to push the boundaries of medical device innovation. Job Description We are seeking a talented Computational Modeling Engineer to join the firm’s Innovation and Design team. In this role, you will apply your expertise in physics, mechanics, or computational modeling to support the development of new medical devices. Your work will focus on creating virtual prototypes and simulations to provide physical insights and predictive data, helping to streamline product development and reduce risk. Responsibilities Contribute to R&D projects by developing and running advanced computational simulations. Develop, validate, and apply physics-based models to optimize design decisions. Strengthen the team’s expertise in computational (bio)physics. Keep up-to-date with the latest modeling techniques and simulation tools. Support innovation initiatives in image-guided therapy, diagnostics, patient monitoring, and personal care by translating application needs into suitable modeling strategies. Requirements -Preferably a PhD in Mechanical Engineering, Applied Physics, or a related field, with experience in computational modeling. -Solid understanding of physics-based modeling of solid mechanics or dynamics. -Experience translating simulation results into insights for engineering and R&D teams. -Curious, innovative, and analytical mindset. -Proactive, flexible, and able to take ownership of technical challenges. -Experience with commercial or open-source simulation tools such as ANSYS, Abaqus, OpenFOAM, or Comsol 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 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  A leading organization in the pharmaceutical industry dedicated to ensuring the highest quality standards in manufacturing and product development. The company operates under strict regulatory guidelines and values excellence, compliance, and continuous improvement. Role Description We are looking for an experienced Quality Assurance Specialist Qualified Person (QP) to oversee and ensure the quality and regulatory compliance of pharmaceutical products. This role involves coordinating product release, managing quality investigations, and supporting inspections and audits to uphold the company’s high standards in production. Responsibilities - Review and approve master documents and specifications to ensure compliance - Initiate and evaluate quality investigations, making release or rejection decisions, and implementing improvement actions - Complete deviation and investigation reports promptly and accurately - Lead quality improvement initiatives to mitigate risks in production processes - Authorize ongoing stability studies and product quality reviews - Prepare for and manage inspections by government agencies and customers, including self-inspections and participation in overseas audits - Handle product complaints, investigate causes, and coordinate recalls when necessary - Maintain communication with external regulators, clients, and partners - Support technology transfer activities and ensure smooth knowledge transfer processes - Provide functional leadership to QA team members, including planning, structuring, and training staff Requirements - Degree in pharmacy, chemistry, biology, or a related field (per art 49 paragraph 2 directive 2001/83/EC) - Over 5 years of experience in aseptic production, with knowledge of lyophilization and visual inspection preferred - Strong understanding of pharmaceutical laws and regulations (EU and US) - Proficiency in analytical methods and automated processes - Decisive, results-oriented, and transparent communicators with a proactive approach 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 global leader in healthcare and pharmaceuticals, dedicated to delivering innovative solutions that improve patient outcomes. They operate within a highly regulated environment, prioritizing quality, compliance, and efficiency across their supply chain operations. Job Description: We are seeking an experienced Regional Supply Chain and Cold Chain Operations Manager to oversee and optimize the distribution of products across the region. The role focuses on ensuring reliable supply, maintaining service levels, and adhering to GDP regulations. The successful candidate will develop and manage cold chain solutions, build strong relationships with supply chain partners, and drive continuous improvement initiatives. Responsibilities: - Ensure the supply meets demand, service levels are maintained, and operations stay within budget, all in compliance with GDP standards. - Develop, select, and implement cold chain solutions within the supply network. - Conduct regular performance reviews with supply chain partners, identify issues, and drive improvements through reporting and escalation management. - Support internal stakeholders by maintaining excellent relationships with third-party logistics providers and escalating issues when necessary. - Manage agreements with supply chain partners, ensuring compliance and performance standards are met. - Identify savings and efficiency opportunities through continuous improvement practices, enhancing quality, performance, and GDP compliance. - Analyze emerging trends or legislative changes that could impact distribution strategies or cold chain practices. - Collaborate with internal teams and participate in projects aligned with regional distribution priorities and initiatives. - Plan, develop, and oversee distribution routes and lanes across the wider region. Requirements: - Master's degree or equivalent in Supply Chain, Logistics, Industrial Engineering, Change Management, or related fields. - Minimum of 5 years’ experience in logistics, with a focus on supplier management and supply chain operations. - Expertise in cold chain logistics, warehousing, and distribution. - Proven project management experience across departments and geographical locations. - Strong track record of supplier management and process improvement. - Excellent analytical skills, with proficiency in tools like MS Excel. - Fluent in English, both written and spoken. - Demonstrated ability to work independently under pressure and within teams. - Strong relationship-building, negotiation, and persuasion skills. - Results-oriented with a strong drive for excellence and continuous improvement. - High sense of responsibility with problem-solving capabilities. - Effective communication 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.

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 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.

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 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.