Validation & Food Safety QA Specialist, Beilen, Drenthe

Company Our client is a well-established, international FMCG manufacturing organisation with a complex supply network. The environment is fast-moving and highly collaborative, with strong focus on customer service, inventory optimisation, product freshness, and continuous improvement across end-to-end supply chain operations. Job Description  We are looking for a Short-Term Supply Network Planner to manage finished goods availability for a defined portfolio across multiple markets and supply locations. This role is central to creating feasible plans, resolving supply/demand exceptions, and coordinating with key stakeholders to protect service levels while balancing cost, inventory, and freshness requirements. Responsibilities - Maintain accurate short-term production plans and communicate updates to factory scheduling teams in a timely way - Own short-term finished goods availability across the assigned portfolio (including semi-finished products where relevant) - Manage product deployments within the assigned supply network based on market needs and stock availability - Identify and resolve exceptions in the 0–12 week horizon (demand vs. supply imbalances), including root cause analysis and corrective/preventive actions - Escalate capacity and material supply risks through the relevant planning governance - Run scenario planning and adjust plans based on constraints such as demand sensing inputs, material availability, stock positions, expiry, allocation rules, and priorities - Monitor service level and inventory exceptions; drive replenishment actions within the distribution network - Follow up on holds, shipments, and past-due elements that impact availability for designated products - Propose inventory rebalancing options (e.g., between warehouses) to improve service and reduce aged stock risk - Support decisions around non-performing inventory movements - Contribute to planning for seasonal activities, activity management, and new product launches - Track, analyse, and report relevant performance metrics to support improvements in cash, cost, and customer service - Own supply-related case fill rate root cause analysis and prevention actions - Support master data set-up and accuracy (including periodic audits) for product, production, and network planning data - Provide back-up support for other planners when needed Requirements - Higher professional education or university degree, ideally with a Supply Chain background - Experience in production planning, short-term planning/S&OE, or supply network planning within a complex environment - Strong analytical skills, including scenario evaluation and structured problem solving - Strong communication skills and confidence working with multiple stakeholders across markets and sites - Fluent English; Dutch is a plus - Comfortable working in a hybrid model with regular on-site collaboration 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 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.

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!

Company  The client is an innovative biopharmaceutical manufacturing organisation working in a highly regulated environment. They deliver critical therapies and operate to strict safety, quality and compliance standards. The site is fast-paced and project-driven, with ongoing investments in equipment, facilities and utilities to support manufacturing operations. Job Description For this Project Manager (BioPharma Engineering) (Capital Projects) position, we are looking for an organised, proactive professional to lead small to medium-sized engineering investment projects on a manufacturing site in the Netherlands. The Project Manager (BioPharma Engineering) (Capital Projects) will manage projects from early definition and feasibility through design, construction and final handover, ensuring delivery meets safety, quality, cost and schedule expectations. Responsibilities - Lead engineering capital projects across equipment, facilities and utilities from definition through handover - Run feasibility studies and translate needs into clear technical scopes and project proposals - Create and execute project plans, coordinating multidisciplinary teams and external partners - Supervise construction and technical execution activities, keeping delivery on track - Align with stakeholders across engineering, operations and project sponsors to support business case development and approvals - Communicate project progress, risks and issues to cross-functional and leadership teams; escalate and drive resolution when needed - Ensure solutions fit site standards and applicable industry requirements - Lead project risk analysis and mitigation planning throughout the project lifecycle - Drive continuous improvement through lessons learned sessions and practical follow-up actions - Prepare and deliver project presentations to support effective phase transitions and stakeholder alignment Requirements  - BSc or MSc degree in Engineering or Technology - Minimum 5 years of technical project management experience, ideally in regulated manufacturing (e.g., pharma, biotech, medical devices, chemical, food, semiconductor) - Strong knowledge of project management tools and methods; experience with planning software is a plus - Understanding of GMP manufacturing environments and regulatory requirements - Familiarity with validation approaches (e.g., GAMP principles and ASTM E2500) and the equipment validation lifecycle (FAT, SAT, IQ, OQ, PQ) - Strong communication and stakeholder management skills, with the ability to lead cross-functional teams - Temporary Full-Time Contract (12 Months) Other Information The role requires a hands-on approach, strong coordination skills and the confidence to drive decisions in a regulated manufacturing environment. If you are interested and want to apply, please submit your application via the apply button below and contact me.

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 Our client is a well-established organisation in the life sciences sector, working on research and development projects that support the creation, testing, and improvement of biological products. The environment is hands-on and collaborative, with strong focus on quality, accurate record-keeping, and working safely and consistently in the laboratory. Job Description We are looking for a Microbiology Technician to support a busy research laboratory in Boxmeer. The Laboratory Research Technician will work across different projects and activities, helping the team deliver reliable laboratory results and maintain accurate documentation. The work is fully on-site and requires flexibility, as the daily tasks can vary based on project needs. Responsibilities - Support laboratory research activities across multiple projects and teams - Perform sample processing and general laboratory tasks as required - Carry out testing activities such as immunoassays (e.g., ELISA/AlphaLISA) and other laboratory experiments - Support bacteriological and virological testing activities, depending on project requirements - Contribute to stability and potency testing activities for biological products - Assist with laboratory work connected to animal studies when needed - Record work accurately and maintain complete laboratory documentation and records - Work in a structured way, follow agreed procedures, and communicate clearly with colleagues and stakeholders Requirements - 2–4 years of relevant laboratory experience - Strong written and spoken Dutch (needed for laboratory documentation and records) - Available for 40 hours per week - Willing and able to work 100% on-site in Boxmeer (5 days per week) - Hands-on experience with one or more relevant techniques/activities such as: ELISA, AlphaLISA, virus titration, bacteriological/virological testing, sample processing, stability testing, or potency testing - Flexible mindset and comfortable working on changing priorities across different projects -Temporary Full-Time 12 Months Contract Other Information This role requires full-time, on-site availability in Boxmeer and offers the chance to contribute to varied laboratory activities in a dynamic research setting. 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 leading organisation within a highly regulated manufacturing environment. The site operates complex production and utility systems and places strong emphasis on safety, quality, and reliable operations. The teams work closely together across production, engineering, and technical services to keep equipment available and maintenance activities well controlled Job Description For our client, we are looking for a Maintenance Work Preparation Coordinator who will prepare and plan preventive and corrective maintenance activities for technicians on site. The role focuses on creating safe, efficient, and well-documented maintenance plans, coordinating permits, and aligning work with production to minimise disruption. Responsibilities - Prepare, prioritise, and plan preventive and corrective maintenance work. - Create and coordinate work permits and required safety documentation, including lock-out/tag-out procedures. - Ensure equipment can be safely shut down and made ready before maintenance activities begin. - Prepare clear work packages, job descriptions, instructions, and supporting documentation for technicians. - Coordinate schedules and align maintenance activities with production planning and site stakeholders. - Arrange required materials, spare parts, tools, and internal/external resources to execute planned work. - Maintain clear communication between technical teams, production, and external parties when needed. - Follow up on progress and support proper documentation and closure of completed maintenance activities. - Support shutdowns, modifications, and improvement initiatives by coordinating preparation and planning. Requirements - Fluent in Dutch (spoken and written). - Experience in maintenance planning and/or work preparation in an industrial production environment. - Strong understanding of work permit processes and safe isolation procedures (lock-out/tag-out). - Technical education at MBO+/HBO level, preferably in Mechanical, Electrical, Automation, or similar. - Strong organisational skills and the ability to coordinate multiple stakeholders. - Clear communication style and a practical, hands-on mindset. - Experience in a regulated environment (e.g., GMP) is a strong advantage. -Temporary Full-Time Contract - 12 Months Other Information The position is fully on-site and involves close collaboration with production and technical teams. The hiring process may include up to two interviews, with on-site meetings preferred. If you are interested and want to apply, please submit your application via the apply button below and contact me.