Quality Assurance Coordinator – Laboratory Operations, Boxmeer, Noord-Brabant

Company Our client is a well-established food production company that manufactures and packs high-quality frozen products. The site operates with strict hygiene and food safety standards and runs a structured shift system to keep production moving efficiently. Job Description We are looking for a Packaging Line Operator (3-Shift) to support daily packaging operations in a fast-paced production environment. The Packaging Line Operator (3-Shift) will operate, set up, and monitor packaging and end-of-line equipment to ensure products are packed safely, correctly, and on time. Responsibilities -Set up, operate, change over, and monitor packaging lines and related equipment (including carton forming and palletising). -Keep product flow running smoothly and adjust when issues or deviations occur. -Perform quality and safety checks and record results according to procedures. -Resolve minor technical issues and involve the technical team when required. -Coordinate day-to-day work with packing colleagues and support operators on the assigned line(s). -Ensure products are packed, processed, and palletised according to the production plan. -Maintain cleanliness, order, and a safe working environment in line with food safety and quality standards. -Participate in shift handovers and communicate clearly with colleagues and supervisors. Requirements -LBO/MBO level of working and thinking. -At least 2 years of relevant experience in a production or packaging environment. -Knowledge of HACCP and food safety practices (including allergens). -Familiar with safety instructions and disciplined working methods. -Comfortable working in a 3-shift rotation (morning, afternoon, night). -Practical, hands-on mindset with basic troubleshooting ability. -Able to coordinate tasks with colleagues and work well in a team. Other Information This role is based on-site and operates in a 3-shift schedule (morning/afternoon/night).  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 life sciences manufacturing site in the Breda area, operating in a highly regulated GMP environment. The business is growing quickly, which means a fast-paced production setting, close cross-functional collaboration, and a strong focus on doing things right first time. Job Description: We are looking for a Senior Quality Assurance Associate to provide hands-on QA support on the shop floor, with a strong focus on packaging and labelling. This is a dynamic role where the successful candidate will be the key quality point of contact for Production, helping to resolve issues in real time while ensuring full GMP compliance. The role also includes batch record review, finished product checks during production, and supporting investigations and deviations. Responsibilities: •    Act as the main QA point of contact for Production during packaging and labelling operations, answering quality-related questions and supporting daily decision-making •    Provide on-the-floor quality oversight during production and perform routine GMP compliance checks •    Review and approve batch record entries before production activities take place and compile/review completed batch records for disposition preparation •    Perform finished product checks during commercial production runs •    Review, approve, initiate, and own deviations as required, and support investigations when issues occur •    Support continuous improvement by contributing to production-related QA projects and site improvement initiatives •    Write, review, and update operational SOPs and work instructions where needed •    Support GMP training activities for QA and Production teams •    Prepare weekly/monthly quality metrics and maintain departmental performance boards •    Build strong working relationships with Production, Warehouse, Maintenance, Engineering, QA Management, and the Qualified Person Requirements: •    BSc or MSc in Pharmaceutical Sciences, Life Sciences, or a related field (strong academic background preferred) •    Around 3 years’ experience in Quality Assurance and/or manufacturing within pharma or medical devices (flexibility for strong recent MSc graduates or relevant internships) •    GMP knowledge is preferred (QA experience in a GMP setting is an advantage but not strictly required); candidates with a QC background are also welcomed •    Experience with batch record review and supporting investigations/deviations is highly beneficial •    Fluent English •    Strong communication, problem-solving, and decision-making skills; able to stay calm under pressure and handle resistance professionally •    Willing to work shifts and fully commit to the current 3-shift rotation and the planned future 5-shift rotation •    Able to commute within approximately 1 hour by car Other Information: This position is based on-site in Breda and requires full commitment to shift work. The current schedule is a 3-shift rotation (early/late/night). A transition to a 5-shift rotation is planned from 01/01/2027 at the earliest, so only candidates who are willing and able to work the future pattern will be considered. 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 global biopharmaceutical organization with a large manufacturing and supply chain operation in Breda. The site supports the production, packaging, storage and distribution of medicines to markets across Europe, Turkey, the Middle East and Africa, operating in a complex and highly regulated environment. Role Description As a Supply Chain – Detailed Scheduler, you will be responsible for managing short-term production planning for packaging lines and ensuring a stable and reliable supply of medicines. You will develop production plans, coordinate activities across departments and remove operational flow stoppers to support timely delivery. Working closely with manufacturing, quality, warehouse and supply chain teams, you will also contribute to continuous improvement, standardization and process automation within the supply planning organization. Key Responsibilities Manage short-term production planning for packaging lines. Create production plans, manage orders and support product launches and phase-in/phase-out activities. Monitor supply chain performance and proactively remove flow stoppers. Measure weekly and monthly KPIs, including MPS stability, and drive improvement actions. Facilitate daily operational meetings and coordinate actions across departments. Lead weekly capacity meetings with manufacturing, quality, warehouse and supply chain stakeholders. Drive standardization, simplification and automation of planning processes. Lead continuous improvement initiatives and root cause analyses. Collaborate cross-functionally to ensure realistic and achievable supply plans. Ensure stable operations and supply chain efficiency while working within GMP and GDP guidelines. Requirements Experience in supply chain planning within a GMP-regulated environment Strong analytical and problem-solving skills. Excellent interpersonal and collaborative skills. Ability to perform root cause analysis and work effectively in a team environment. Strong interest in standardization, process improvement and automation. Experience or interest in tools such as Tableau, Smartsheet, Databricks or RPA is preferred. Detail-oriented and able to coordinate multiple priorities. Willingness to work at least 3 days per week on-site in Breda.

About Our Client Our client is a global healthcare and pharmaceutical organization dedicated to developing and delivering innovative medicines that improve patients’ lives worldwide. Its Leiden site is an important biopharmaceutical manufacturing and supply hub, operating in a highly regulated environment where quality, reliability, and continuous improvement are essential. About the Position We are looking for a Logistics Process Owner to take ownership of material supply processes at a biotherapeutics site in Leiden. In this role, you will look at how materials move through the warehouse, distribution, and supply processes, identify where things can be improved, and help implement more efficient and reliable ways of working. You will work closely with warehouse, distribution, operations, and planning teams and use data and process insights to improve performance. The role combines logistics, process improvement, documentation, stakeholder management, and continuous improvement. Responsibilities Take ownership of material supply and related logistics processes. Analyze existing processes to identify inefficiencies, bottlenecks, risks, and improvement opportunities. Develop, update, and maintain SOPs and other process documentation. Ensure documentation remains accurate, compliant, and reviewed on time. Work with warehouse, distribution, operations, and planning teams to solve process issues. Identify opportunities to improve logistics processes through technology, automation, WMS/TMS, and other digital solutions. Define and monitor KPIs to measure process performance. Use data and performance trends to identify improvement opportunities and support decision-making. Drive continuous improvement initiatives and help implement sustainable process changes. Communicate process improvements and align stakeholders across different teams. Requirements Bachelor’s degree in Logistics, Supply Chain, Industrial Engineering, or a related field. 2+years of experience in logistics, supply chain optimization, process improvement, or a comparable role. Strong analytical and problem-solving capabilities. Experience analyzing processes and translating findings into practical improvements. Strong attention to detail, particularly around data and process documentation. Experience working with SOPs and within a regulated or quality-driven environment. Good knowledge of logistics systems, data analysis tools, and Microsoft Office, particularly Excel and PowerPoint. Strong communication and stakeholder management skills. Comfortable working with multiple teams and managing different priorities. Fluent in English; Dutch is a strong advantage. Lean/Six Sigma knowledge or certification is a plus. Willingness to work five days onsite in Leiden.

The Company Our client is one of the leads from the Biotechnology industry who try to improve patients’ lives, by distributing their medicines to hospital and pharmacies in 100 different countries in the world, to over 10 million patients, in Europe, Turkey, Middle East and Africa Regions. Role Description As a Production Operator, you will be responsible for operating and maintaining semi-automated production and packaging lines within a GMP-regulated manufacturing environment. You will ensure production processes run safely, efficiently, and in compliance with quality standards while supporting continuous improvement initiatives and minimizing production downtime. Responsibilities Run and oversee production machines to keep operations running smoothly. Prepare equipment for new production batches and switch products when needed. Spot and fix minor machine issues to reduce downtime. Enter and update production records using the company's systems. Help investigate production issues and support practical solutions. Suggest ideas to improve efficiency, quality, and daily operations. Follow safety, quality, and company procedures at all times. Work closely with your team to achieve daily production goals. Requirements A technical background or hands-on experience in a production or manufacturing environment. Previous experience working with production machinery or automated equipment. Comfortable troubleshooting basic machine or process issues. Experience in industries such as pharmaceuticals, biotechnology, food, medical devices, or other regulated environments is a plus. Familiarity with production systems such as SAP or similar software is an advantage. A proactive mindset with a willingness to learn and improve processes. Good communication skills in English. Willingness to work rotating 3-shift or 5-shift schedules. Other Information This is an excellent opportunity to join a global, high-tech manufacturing environment where you'll work with advanced automation technologies while developing your technical skills and career. A competitive salary, shift allowances, bonus, 13th-month salary, holiday allowance, and excellent development opportunities are offered. Apply to our vacancy for more information. We look forward to hearing from you!

About the Company Our client is a global biopharmaceutical organization with a highly regulated manufacturing environment. The production site focuses on the safe and consistent manufacturing and packaging of medicines, with a strong emphasis on quality, compliance and operational excellence. Role Description As a Technical Operator – Manual Lines, you will execute manual production and packaging activities within a GMP-regulated manufacturing environment. You will work according to strict procedures and SOPs, perform quality checks and ensure accurate documentation throughout the production process. With a strong focus on consistency, accuracy and compliance, you will contribute to a safe and efficient production flow while working closely with your team. Key Responsibilities Execute manual production and packaging activities according to SOPs and established procedures. Perform in-process quality checks and ensure products meet applicable requirements. Complete batch records, logs and other GMP documentation accurately and on time. Identify and report deviations and quality issues and support their resolution. Participate in triage and problem-solving activities with Production and QA. Perform production set-up and close-down activities. Execute daily, weekly and monthly cleaning activities. Maintain a safe, clean and compliant working environment. Perform repetitive manual production tasks with consistency and accuracy. Collaborate with colleagues to maintain a smooth and efficient production process. Requirements Basic understanding of GMP, SOPs and production processes. Strong quality focus and attention to detail. Good manual dexterity and ability to maintain a consistent work tempo. Highly disciplined and comfortable working according to strict procedures. Reliable, accurate and consistent in repetitive production activities. Strong compliance mindset. Fluent in English. Willingness to work in a 2-shift system and commute to Breda. Experience with ERP systems such as SAP/MES is an advantage.

About the Company Our client is an international food production organization specializing in frozen food products. Within a structured production and packaging environment, the organization focuses on delivering safe, high-quality products while maintaining efficient production processes and strong food safety standards. Role Description As an All-round Packing Operator, you will be responsible for operating, setting up, changing over and monitoring various packaging, box forming and palletizing systems. You will use your technical knowledge to resolve minor technical issues, monitor product quality and ensure a smooth production flow. Working closely with packing staff, assistant operators and supervisors, you will contribute to safe, efficient and high-quality production in a 3-shift environment. Key Responsibilities Set up, operate, change over and monitor packaging, box forming and palletizing systems. Perform quality and safety checks and accurately record results. Monitor product flow and make adjustments when deviations or malfunctions occur. Resolve minor technical breakdowns and involve the Technical Service when required. Coordinate daily activities with packing staff and assistant operators on assigned lines. Ensure correct processing, packaging and palletizing according to the production schedule. Follow applicable food safety, quality and hygiene procedures. Contribute to an orderly, clean and safe working environment. Participate actively in shift handovers and communicate relevant information clearly. Support smooth production and contribute to achieving planned production orders. Requirements At least 2 years of relevant experience in a production or packaging environment. Knowledge of HACCP and Food Defense. Experience or ability to provide and follow safety instructions. Experience with or willingness to participate in on-the-job training. Knowledge of allergens and food safety requirements. Technical understanding and a hands-on approach to resolving minor breakdowns. Able to work effectively with colleagues in a production and shift environment. Structured and quality-focused approach to working. Willingness to work in a 3-shift system: 07:15–15:15, 15:15–23:15 and 23:15–07:15.

Over het bedrijf Onze opdrachtgever is een internationale farmaceutische organisatie die actief is binnen een sterk gereguleerde omgeving, met een sterke focus op productkwaliteit, compliance en continue verbetering binnen productie- en kwaliteitsprocessen. Functieomschrijving Als QA Officer ondersteun je diverse Quality Assurance-activiteiten binnen een GMP-gereguleerde farmaceutische of biotechomgeving. Je draagt bij aan het behandelen van afwijkingen en CAPA's, root cause investigations, validatie- en kwalificatieactiviteiten en het beoordelen van kwaliteitsdocumentatie. Je werkt nauwkeurig volgens vastgestelde kwaliteitssystemen en schakelt effectief met verschillende interne en cross-functionele stakeholders. Belangrijkste verantwoordelijkheden Ondersteunen bij het behandelen en onderzoeken van GMP-afwijkingen. Bijdragen aan het opstellen, implementeren en opvolgen van CAPA's. Ondersteunen van root cause investigations met passende onderzoeksmethodieken. Deelnemen aan validatie- en kwalificatieactiviteiten. Beoordelen van GMP-documentatie op juistheid en compliance. Ondersteunen van Quality Assurance-activiteiten binnen farmaceutische of biotechproductie. Samenwerken met verschillende afdelingen rondom kwaliteits- en compliancevraagstukken. Zorgdragen voor een correcte en volledige documentatie van kwaliteitsactiviteiten. Functie-eisen Een relevante bacheloropleiding of gelijkwaardig niveau binnen een wetenschappelijke, farmaceutische of technische richting. Aantoonbare ervaring binnen een GMP-gereguleerde Sterke ervaring met deviations, CAPA's en root cause investigations. Ervaring met validatie en kwalificatie. Ervaring met het beoordelen van GMP-documentatie. Goede kennis van GMP-principes en kwaliteitssystemen. Vloeiende beheersing van Nederlands en Engels, zowel mondeling als schriftelijk.

Company Our client is a large, international organisation in a highly regulated life-sciences environment. They run complex operations where quality, compliance, and reliable supply processes are critical. The culture is structured, collaborative, and focused on continuous improvement. Job Description For our client, we are looking for a Logistics Process Owner (Materials Supply) to take ownership of key material supply and replenishment processes at their site in Leiden. This role sits close to operations and has direct impact on manufacturing performance, so it requires someone who is hands-on, detail-focused, and confident working in a compliance-driven setting. Responsibilities -Own and improve end-to-end material supply and replenishment processes for the site -Analyse current logistics workflows to identify bottlenecks, risks, and improvement opportunities Develop, maintain, and review SOPs and process documentation in line with GDP/GMP expectations -Collaborate with warehouse, operations, and other cross-functional stakeholders to ensure smooth material flow -Define, track, and report KPIs to monitor process performance and drive improvements -Support continuous improvement initiatives using Lean / operational excellence principles -Use systems and data tools to monitor performance and support decision-making (e.g., ERP and reporting tools) Requirements -Several years of hands-on experience in logistics/materials supply within a regulated manufacturing environment (GDP/GMP) -Strong process ownership mindset: able to build, implement, and sustain processes (not only analyse) -Experience writing and maintaining procedures / SOPs -Lean / continuous improvement skills (Lean Six Sigma is a strong advantage) -Comfortable working with ERP systems and data/reporting tools (SAP knowledge is a plus) -Strong English communication skills: Dutch is a plus -Able to work full-time on-site in Leiden Other Information If you are interested and want to apply, please submit your application via the apply button below and contact me.