Customer Logistics Coordinator, Veghel, Noord-Brabant

Company For an international organization in the life sciences sector, we are looking for a hands-on laboratory professional to support ongoing research and testing activities. The environment is quality-driven, documentation-heavy, and highly collaborative, with close cooperation across multiple teams and projects. Job Description We are looking for a Laboratory Research Technician to join a busy on-site laboratory team in Boxmeer. The role focuses on practical lab support across a variety of techniques and projects, rather than one fixed routine. The successful candidate will contribute to reliable test execution, accurate documentation, and flexible support where the lab needs it most. Responsibilities - Support daily laboratory activities across changing research priorities and multiple teams. Perform sample processing and help ensure correct labelling, handling, and traceability. - Carry out and/or support laboratory tests such as ELISA and AlphaLISA. - Support microbiological and virological work, including activities such as virus titration and related testing. - Contribute to stability and potency testing activities (including work linked to vaccines). - Assist with preparation and support during animal-study related lab activities where required. - Maintain accurate documentation and laboratory records, following procedures and local documentation standards. - Work fully on site and collaborate closely with colleagues to deliver timely, high-quality lab output. Requirements - 2–4 years of relevant laboratory experience. - Fluent in Dutch (required for documentation and lab records). - Comfortable working in a flexible role where tasks vary by project and team needs. - Hands-on experience with one or more relevant techniques (e.g., ELISA/AlphaLISA, sample processing, virology/bacteriology testing, virus titration, stability testing). - Accurate, detail-oriented, and confident working with structured documentation. - Able and willing to work 100% on-site in Boxmeer. 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 an international organization operating across multiple markets, with a strong focus on developing its people, strengthening organizational capabilities and building a future-ready workforce. Learning, development and talent transformation are key priorities within its HR strategy. About the Role We are looking for an experienced Senior Learning & Development Digital Ecosystem Lead to lead several high-priority Learning & Development initiatives. In this strategic role, you will take primary ownership of the Digital Learning Ecosystem and contribute to the organization-wide Skills Program. You will also lead the implementation of SHL development assessments and coordinate selected High Performing Team interventions across EMEA. Working closely with Digital HR, internal L&D teams, HR stakeholders, business leaders and external partners, you will provide strategic direction, drive project delivery and ensure that learning initiatives align with wider organizational capability priorities. Responsibilities - Lead the L&D roadmap and program delivery for the Digital Learning Ecosystem. - Provide direction to internal teams and coordinate project planning and execution with Digital HR and external vendors. - Drive improvements in digital learning technologies, learner experience, accessibility and adoption. - Represent Learning & Development within the organisation's Skills Programme. - Translate workforce skills requirements into learning, upskilling and reskilling initiatives. - Ensure L&D requirements are incorporated into skills governance, taxonomy, architecture and operating model decisions. - Lead the implementation, rollout and adoption of SHL development assessment solutions. - Support assessment-related policies, governance, stakeholder communication and the transition from existing assessment providers. - Coordinate High Performing Team interventions across EMEA, supporting stakeholders and facilitators throughout the process. - Monitor program progress, evaluate outcomes and ensure follow-up actions are delivered. Requirements - Extensive experience in senior Learning & Development, Talent Development or HR transformation roles. - Proven track record of leading strategic, organization-wide L&D programs and complex projects. - Strong knowledge of digital learning ecosystems, LMS/LXP platforms and learning technologies. - Experience with skills-based organizations, skills frameworks, workforce capability development or skills transformation. - Experience implementing talent or development assessment solutions; SHL or comparable assessment platforms are an advantage. - Strong stakeholder management experience, working with senior business leaders, HR teams, Digital HR and external vendors. - Experience managing cross-functional and international programs. - Excellent communication, leadership and influencing skills. - Strategic mindset combined with a hands-on approach to program implementation and delivery. Other Information If you are interested in this opportunity, please submit your application via the apply button below and contact us for further information.

The Company Our client is an international organization operating in the food and nutrition industry, with a strong focus on producing high-quality ingredients and nutritional products for customers worldwide. Quality, food safety and continuous improvement are central to its operations. About the Role As a QA Validation Specialist, you will play an important role in maintaining and improving the validation management system at the production site in Beilen. Working within the Local Quality Assurance team, you will act as the main point of contact for validation-related matters and represent Quality Assurance in technical, engineering and packaging projects. Responsibilities - Develop, implement, maintain and continuously improve the validation management system and related documentation. - Represent Quality Assurance in validation activities, technical projects and packaging projects. - Develop, execute and periodically review the Site Validation Master Plan. - Translate quality policies and requirements into practical procedures and documentation. - Advise employees and management on quality, food safety and quality management systems. - Support and verify CAPA activities and change management processes. - Conduct internal audits and support external audits. - Provide training on quality and food safety topics. - Act as a Subject Matter Expert for assigned quality-related topics. - Monitor developments in quality standards and regulations and translate them into practical improvements. Requirements - HBO or academic working and thinking level. - Several years of experience within the food, dairy or pharmaceutical industry. - Knowledge of HACCP, FSSC, GMP+ and relevant quality and food safety regulations. - Proven experience with validation processes and quality management systems. - Experience working on cross-functional projects. - Familiarity with systems such as SharePoint, SAP, KMS and MS Office. - Strong analytical and problem-solving skills with a continuous improvement mindset. - Excellent communication and stakeholder management skills. - Able to work independently and confidently advise different levels of the organization. Other Information If you are interested in this opportunity, please submit your application via the apply button below and contact us for further information.

About the Company Our client is a large, international production organisation in the food sector. The site manufactures ingredients and nutrition products for global B2B and B2C markets. Quality and food safety are central, and the QA team works closely with Production, Engineering, Technology, Maintenance, R&D and Continuous Improvement, as well as external stakeholders such as auditors, suppliers and certification bodies. Job Description For a production site in Beilen (Netherlands), our client is looking for a Validation & Food Safety QA Specialist to strengthen the local Quality Assurance team. This role focuses on building, maintaining and improving the site’s validation management system and ensuring processes consistently meet quality and food safety requirements. The Validation & Food Safety QA Specialist acts as the key QA contact for validation topics and represents QA in technical and packaging-related projects. Responsibilities -Set up, integrate, maintain and continuously improve the validation management system and related documentation. -Develop, execute and periodically review the Site Validation Master Plan. -Represent Quality Assurance in validation activities and in technical/packaging projects to ensure compliance with quality and food safety standards. -Translate quality policies into practical, workable procedures within the factory environment. -Advise employees and management on quality, food safety, and the quality management system. -Support and verify CAPA actions and contribute to effective change management. -Perform internal audits and support preparation and follow-up of external audits. -Provide training and guidance on quality and food safety topics to support operational teams. -Act as a Subject Matter Expert (SME) for assigned QA topics and actively track developments in the field, translating them into site improvements. Requirements -Higher professional education level (HBO) or academic level, preferably in a relevant discipline. -Several years of QA experience in a food and/or pharma manufacturing environment. -Solid hands-on experience with validation processes and quality management systems. -Knowledge of food safety and quality standards such as HACCP, FSSC, GMP+ and related regulations. -Comfortable working in a project environment and with cross-functional stakeholders. -Strong analytical skills, a continuous improvement mindset, and the confidence to challenge and escalate when needed. -Good communication skills and stakeholder management ability. -Able to work in Dutch and English. 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 operating in a highly regulated production environment. The organisation uses advanced automated manufacturing and packaging technologies to deliver high-quality products while maintaining strong standards for safety, compliance, and operational excellence. The site values teamwork, continuous improvement, technical expertise, and innovation. Job Description We are looking for a Manufacturing Operator to join a dynamic production team. In this role, you will help keep semi-automated production and packaging lines running safely, efficiently, and according to GMP requirements. You will monitor equipment, handle basic technical issues, complete production activities, and support the team in keeping production running smoothly. Roles & Responsibilities - Run and monitor semi-automated production and packaging lines in a GMP environment. - Set up and start production equipment according to SOPs and production instructions. - Check and adjust machines and process settings when needed. - Carry out cleaning, product changeovers, line clearance, and basic equipment checks. - Identify and troubleshoot machine or process issues to reduce production downtime. - Make basic machine adjustments to keep the production process running smoothly. - Record and verify production information in SAP, MES, and other manufacturing systems. - Complete batch records, equipment logs, and other production documentation accurately. - Check product quality during production and report deviations or abnormalities. - Perform first-line checks and basic maintenance when required. - Follow GMP, SOPs, safety rules, and site procedures at all times. - Coordinate with Production, Maintenance, and Quality teams to resolve technical or production issues. - Support root cause investigations using methods such as 5 Why and RCA. - Contribute to continuous improvement initiatives using Lean and Kaizen principles. - Communicate clearly during shift handovers and share relevant production information with colleagues. Requirements - Technical education at MBO level or an equivalent qualification such as VAPRO B. - Experience in automated production, assembly, packaging, or process manufacturing. - Good technical understanding and the ability to identify and solve production issues. - Familiarity with RCA, 5 Why, Lean, or Kaizen is an advantage. - Experience in GMP or another regulated manufacturing environment is highly desirable. - Knowledge of SAP, MES, or similar production systems. - Good communication skills in English. - Willingness to work rotating 3-shift and 5-shift schedules. - Available for a temporary full-time contract (1 year). Why Apply? This role is a great opportunity for someone who enjoys working with modern manufacturing technology and solving technical production challenges. If you're ready 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.

The Company Our client is a leading dairy cooperative with a global presence and a rich 150+ year history. They focus on producing high-quality nutritional ingredients and dairy solutions, and are strongly committed to innovation, sustainability and operational excellence within a highly automated and hygienic production environment. Job Description As a Supply Chain Project Manager, you will lead supply chain integration projects, focusing on integrating production sites into existing Supply Planning, Scheduling and S&OP processes. You will collaborate with cross-functional teams across the Netherlands and Belgium to drive process improvements, support the new Milkpowder strategy and ensure alignment between operational and long-term supply chain planning. Responsibilities Lead and support the integration of a supply network into Supply Planning, Scheduling and MRP processes. Drive the integration into the Butter and Milk Powder S&OP cycle. Align planning activities across sites, departments and key stakeholders. Translate strategic objectives into effective planning and supply chain processes. Support the implementation of the new milk powder strategy. Manage projects from initiation through to completion, establishing clear frameworks and maintaining progress. Bring colleagues and stakeholders together and create support for changes across different organisational levels. Work with both operational and tactical planning processes. Requirements Bachelor’s or Master’s degree, preferably in Supply Chain Management. Experience with S&OP, Rough-Cut Capacity Planning, MPS, MRP and inventory management principles. Proven experience in supply chain projects, network integrations or business transformation programmes. Experience working in a matrix organisation and with multifunctional teams. Strong analytical and decision-making skills. Clear communication skills and the ability to work with stakeholders at all organisational levels. A proactive, decisive and adaptable approach. Fluent in English and Dutch Other Information Apply to our vacancy for more information. We look forward to hearing from you!

About the Company Our client is a large, highly regulated life-sciences organisation with an active site in the Netherlands. With many facility and engineering projects running at the same time, the business relies on strong change control, clear documentation, and close collaboration between Engineering, Quality, Safety, and operations. Role Description We are looking for a Quality Change Control & Commissioning Specialist. This role leads change control activities within quality and safety systems and supports commissioning work for facility infrastructure and technical assets. The Quality Change Control & Commissioning Specialist will coordinate impact assessments, drive stakeholder alignment, and ensure change records are followed through from initiation to closure in a live operational environment. Responsibilities -Initiate, manage, track, and close change control records within quality and safety systems. -Perform pre-assessments and impact assessments for engineering and facility changes. -Evaluate potential impact on GMP-relevant processes, safety, operations, and supporting documentation. -Coordinate information gathering, reviews, approvals, and follow-up actions with Quality, Safety, Engineering, and technical asset owners. -Maintain accurate, complete, and audit-ready change documentation. -Support commissioning activities for facility infrastructure and technical assets (e.g., HVAC, utilities, electrical systems, fire safety systems, and building finishes such as floors, walls, and ceilings). -Manage priorities effectively across multiple concurrent projects and stakeholders. Requirements -Strong experience in change control / change management, ideally in a GMP-regulated environment. -Experience working with quality and safety management systems; familiarity with electronic quality systems (e.g., Veeva-type tools) is a strong advantage. -Solid background in impact assessment and structured documentation management. -Confident stakeholder manager who can work independently and take ownership. -Fluent English; Dutch is a plus. 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 manufacturing organisation operating in a highly regulated environment. Quality, food safety, and continuous improvement are central to how the site works, with close collaboration between Quality Assurance, Production, Engineering, and R&D. Job Description The QA Validation Specialist (Food Manufacturing) will strengthen site quality and food safety by leading validation activities and developing the site’s validation approach and documentation. The role acts as the main point of contact for validation topics and represents Quality Assurance in technical and packaging-related projects, ensuring processes and changes remain compliant and well controlled. Responsibilities - Set up, maintain, and continuously improve the site validation management system and related documentation - Own and execute the Site Validation Master Plan and coordinate periodic reviews - Represent Quality Assurance in validation trajectories, technical projects, and packaging projects - Translate quality policies into practical site documentation and working standards - Advise teams and stakeholders on quality, food safety, and quality management system requirements - Support change management and CAPA follow-up, including verification of effectiveness - Perform internal audits and support external audits (e.g., certification or customer audits) - Deliver training and guidance on quality and food safety topics - Act as a subject matter expert for assigned quality topics and stay up to date with relevant developments Requirements - Bachelor’s or Master’s level working and thinking capability (or equivalent experience) - Several years of experience in food manufacturing and/or pharmaceutical environments - Hands-on knowledge of validation practices and quality management systems - Solid understanding of food safety and quality standards (e.g., HACCP and GFSI-related standards) and relevant regulations - Experience working in cross-functional project settings - Strong analytical skills and a proactive, improvement-driven mindset - Clear communication skills, able to influence and work with multiple departments - Comfortable working with common documentation and enterprise systems (e.g., MS Office and quality/process documentation tools) Other Information If you are interested and want to apply, please submit your application via the apply button below and contact me.

Company A global, highly regulated manufacturing environment where quality, safety, and compliance are central to daily operations. The site works under strict GMP standards and follows detailed procedures to ensure reliable, audit-ready performance across production and support functions. Job Description For our client, we are looking for a Validation & Calibration Engineer to support validation and calibration activities on site. The role combines hands-on technical work with strong documentation responsibilities, ensuring equipment and processes remain compliant, accurate, and ready for inspection. Responsibilities - Execute validation and calibration activities in a GMP environment, following SOPs and work instructions. - Work with temperature measurements and process equipment, ensuring accurate results and traceable records. - Prepare and maintain clear technical documentation, including reports and supporting evidence. - Support compliant operation of site equipment and utilities by identifying issues, documenting findings, and following up on required actions. - Work independently on site while coordinating effectively with relevant stakeholders to keep work aligned and compliant. - Contribute to structured, accurate documentation in both Dutch and English, including Dutch-language procedures and reports. - Apply knowledge of autoclaves where relevant to validation/calibration activities. Requirements - Higher vocational level education (HBO) or equivalent. - Proven experience in a GMP/pharmaceutical manufacturing environment. - Hands-on experience with validation, calibration, and technical documentation. - Fluent Dutch (required) and good English skills. - Ability to work accurately, independently, and in a structured way. - Experience with autoclaves and/or process equipment and temperature measurements is a strong advantage. Other Information The work is performed fully on site in Boxmeer, and the interview process typically consists of 2 to 3 conversations, with a preference for face-to-face meetings.  

Company Our client is a large, highly regulated organization within the pharmaceutical sector, operating a modern production site where quality, compliance, and safety are critical. The site works under GMP standards and relies on robust processes, clear documentation, and well-maintained equipment to ensure reliable operations. Job Description For an on-site role in Boxmeer (Netherlands), we are looking for a GMP Validation & Calibration Specialist who can independently support validation and calibration activities in a GMP environment. The GMP Validation & Calibration Specialist combines hands-on technical work with strong documentation skills, ensuring all work is executed in line with SOPs and work instructions and recorded accurately in both Dutch and English. Responsibilities Perform validation and calibration activities on-site within a GMP pharmaceutical environment. Work strictly according to SOPs and work instructions, ensuring consistent compliance. Prepare, maintain, and deliver clear technical documentation, reports, and records with a high level of accuracy. Support reliable and compliant operations by recording results precisely and following good documentation practices. Support activities involving temperature measurements and process equipment; autoclave-related knowledge is relevant to the work. Communicate effectively in both Dutch and English, including working with Dutch-language procedures and documentation. Requirements Completed HBO-level education (or equivalent). Proven experience in a GMP/pharmaceutical environment. Hands-on experience with validation, calibration, and technical documentation/reporting. Fluent Dutch (required) and strong English skills (spoken and written). Able to work accurately and independently, with enough experience to be productive quickly in an autonomous role. Nice to have experience with autoclaves, temperature measurements, and process equipment. Other Information: If you are interested and want to apply, please submit your application via the apply button below and contact me.