QA Specialist, Beilen, Drenthe

Over het Bedrijf Sluit je aan bij een toonaangevende internationale producent in de voedingsmiddelenindustrie die investeert in de uitbreiding en modernisering van haar productiefaciliteiten. Binnen een groot investeringsproject speel je een cruciale rol in de succesvolle Commissioning & Start-Up van een nieuwe productielijn en zorg je voor een soepele overgang van de bouwfase naar commerciële productie. Rolomschrijving Als CSU Manager ben je verantwoordelijk voor het leiden van de volledige Commissioning & Start-Up-fase van een groot investeringsproject, waarbij een nieuwe UHT-installatie, homogenisator en aseptische opslagtank worden geïnstalleerd. Je ontwikkelt en implementeert de CSU-strategie, coördineert kwalificatie- en validatieactiviteiten en zorgt ervoor dat alle betrokken partijen gedurende het gehele traject optimaal samenwerken. Je combineert technische expertise met sterk stakeholdermanagement en een gestructureerde aanpak van documentatie en projectuitvoering. Belangrijkste Verantwoordelijkheden Ontwikkelen, beheren en uitvoeren van de volledige Commissioning & Start-Up-strategie Leiden van de CSU-fase vanaf mechanical completion tot en met commerciële productie Coördineren van kwalificatie- en validatieactiviteiten conform project- en klantvereisten Fungeren als belangrijkste aanspreekpunt voor projectteams, operations, quality, leveranciers en klanten Beoordelen en kritisch analyseren van de projectplanning en het identificeren van risico's en verbeterpunten Opstellen van een realistische planning, mijlpalen en CSU-roadmap Zorgen dat klantacceptatiecriteria worden geïntegreerd in de commissioningstrategie Onderhouden van communicatie met klanten over projectvoortgang, planning en oplevering Waarborgen van volledige en correcte projectdocumentatie gedurende commissioning en validatie Bijdragen aan een veilige, efficiënte en succesvolle projectuitvoering Vereisten HBO- of WO-opleiding in Werktuigbouwkunde, Procestechnologie, Food Technology, Engineering of een vergelijkbare technische richting Aantoonbare ervaring als Commissioning & Start-Up (CSU) Manager binnen grootschalige investeringsprojecten Grondige kennis van commissioning, kwalificatie, validatie en start-up processen Ervaring binnen de voedingsmiddelen-, zuivel-, farmaceutische-, dranken- of procesindustrie (ervaring binnen de zuivel is een sterke pré) Sterke stakeholdermanagementvaardigheden en ervaring met klantgerichte projecten Uitstekende plannings-, documentatie- en risicomanagementvaardigheden Ervaring met het aansturen en coördineren van multidisciplinaire projectteams In het bezit van een VCA-certificaat (VCA-VOL is een sterke pré) Goede beheersing van zowel de Nederlandse als Engelse taal Bereid om voornamelijk op locatie te werken en indien nodig incidenteel mee te draaien tijdens de opstartfase Opdrachtdetails Start: Zo snel mogelijk Eerste fase: 1–2 dagen per week (2026) Vanaf Q4 2026: 4–5 dagen per week tot en met Q2 2027 Standplaats: Nuenen (voornamelijk op locatie) ZZP'ers zijn welkom Opdrachtduur: Circa 9 maanden (voor ZZP in contracten van 6 maanden)

About The Company Our client is a leading global FMCG organization seeking a Response Planner to join its Integrated Planning team. This role is responsible for balancing short-term demand and supply, improving customer service, reducing business waste, and driving continuous planning improvements. Role Description As a Response Planner, you will manage the short-term (up to 6 weeks) demand and supply reconciliation process to ensure product availability while minimizing inventory waste. You will collaborate with cross-functional teams to manage service risks, optimize stock allocation through AATP Business Rules, and support continuous improvement initiatives with Genpact. Key Responsibilities Drive short-term demand and supply reconciliation. Manage service risks and customer order priorities. Own and maintain AATP Business Rules. Reduce excess, blocked, residual, and obsolete inventory. Support continuous improvement and root cause analysis. Collaborate with Sales, Customer Service, Market Supply Planning, and Genpact. Key Requirements Bachelor's degree in Supply Chain, Business, Engineering, or a related field. Experience in Response Planning, Supply Planning, or Integrated Planning. Knowledge of SAP S/4HANA, AATP, and planning tools (Kinaxis preferred). Strong analytical, stakeholder management, and communication skills. Interested? Click the application link below to submit your application and take the next step in your career.  

Company: A leading organization in the pharmaceutical industry dedicated to maintaining the highest standards of quality and safety in its research and production processes. Committed to innovation and compliance, the company provides a dynamic environment for professionals to contribute to impactful projects. Job Description: We are seeking a reliable and detail-oriented Quality Assurance Coordinator to support laboratory quality systems. The role involves ensuring regulatory compliance, managing quality data, and supporting GMP standards within the laboratory environment. Responsibilities: - Ensure the timely and accurate processing of regulatory changes within quality systems such as SAP, LIMS, and MS Office. - Maintain GMP compliance across all activities. - Collaborate closely with Qualified Persons and internal teams to facilitate quality assurance processes. - Support the implementation and documentation of quality procedures and updates. - Assist in audits and inspections related to quality standards. - Contribute to continuous improvement initiatives related to quality management. Requirements: - Minimum of 1 year of relevant work experience in a quality or laboratory environment. - Dutch language skills are essential; fluency in English is required. - Higher vocational education (HBO) in biochemistry, microbiology, or a related field. - Experience with SAP and knowledge of GMP/GDocP are preferred. Other Information: If you are interested and want to apply, please submit your application via the apply button below and contact me.

The Company A leading organization in the pharmaceutical and animal health sector, operating across multiple locations in the Netherlands. The company is known for its strong focus on safety, compliance, and innovation within engineering and production environments Role Description We are seeking a skilled QC Transfer Specialist to join our Animal Health division. In this role, you will ensure the successful transfer and validation of biological and analytical tests related to vaccines and pharmaceuticals. You will play a key part in transferring new tests from R&D or other sites into our quality control labs, ensuring compliance with GMP standards and meeting transfer timelines. Responsibilities -Lead and support the transfer of biological and analytical tests for vaccines and pharmaceutical products, ensuring reproducibility and quality. -Manage transfer projects, whether introducing new tests or transferring existing ones from R&D or other sites, within set timeframes. -Perform and validate transfer tests, support testing of post-transfer samples, and coordinate with the QC team for seamless integration. -Act as the primary contact for deviations, changes, audits, training, and documentation related to transfers, adhering to GMP procedures. -Collaborate with R&D and other sites to ensure smooth transfer processes and continuous improvement initiatives using Lean Six Sigma tools. -Monitor transfer progress, escalate issues when necessary, and drive towards timely completion of projects. Requirements -HBO education or higher in microbiology, analytical chemistry, or a related laboratory field. -Minimum of 5 years’ experience in a biological QC or similar lab environment, preferably within a GMP or GLP setting. -Proven experience with transfer processes, project management, and data analysis. Familiarity with SAP, LIMS, or similar electronic data systems. -Certification or experience with Lean Six Sigma, problem-solving, and root cause analysis is a plus. Accurate, solution-oriented, and able to work independently as well as part of a team. -Strong communication skills in English and Dutch, both written and spoken. 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 biotechnology company dedicated to improving patients' lives through innovative medicines. The Breda manufacturing site is a highly automated, GMP-regulated facility responsible for the production, labeling, assembly, and distribution of medicines to more than 75 countries worldwide. The company values innovation, operational excellence, continuous improvement, and collaboration while providing employees with excellent career development opportunities. Job Description: As a Technical Operator (GMP) – Automated Manufacturing, you'll play an important role in the day-to-day running of our manufacturing operation. Working within a GMP-regulated environment, you'll help ensure products are produced safely, efficiently, and to the highest quality standards. You'll work with advanced production equipment, support troubleshooting activities when issues arise, and help keep manufacturing processes running smoothly. Whether it's operating equipment, carrying out routine checks, recording production data, or identifying improvements, you'll be a key part of a team focused on delivering reliable results. This position is ideal for someone who enjoys a hands-on technical role, likes solving problems, and wants to contribute to a modern manufacturing environment where quality, safety, and continuous improvement are at the heart of everything we do. Responsibilities: Ensure production activities are completed according to GMP, quality, and safety standards. Operate automated equipment used for manufacturing, assembly, labeling, and packaging activities. Prepare production lines for new batches, including equipment set-up, changeovers, cleaning, and line clearance activities. Review and record manufacturing data using digital systems such as SAP and Manufacturing Execution Systems (MES). Investigate process deviations and support Root Cause Analysis (RCA / 5 Why) to prevent recurring issues. Identify opportunities to improve workflows, equipment performance, and operational efficiency through Lean Manufacturing and Continuous Improvement initiatives. Work closely with colleagues from Production, Engineering, Maintenance, and Quality teams to solve day-to-day operational challenges. Perform routine inspections, equipment adjustments, and basic first-line maintenance tasks. Monitor production performance and take appropriate action when abnormalities occur. Support a culture of teamwork, innovation, operational excellence, and continuous improvement. Requirements: This opportunity is ideal for someone who enjoys working in a technical environment, likes finding practical solutions, and takes pride in maintaining high standards of quality and compliance. We'd love to hear from you if you have: MBO-level technical qualification or equivalent experience. Experience working within manufacturing, production, processing, or other industrial operations. Experience operating or supporting automated machinery or technology-driven production environments. Strong problem-solving skills with a structured approach to troubleshooting. Previous experience within a GMP-regulated or other quality-controlled industry, such as pharmaceuticals, biotechnology, medical devices, food production, or chemicals. Knowledge of GMP requirements and quality-focused ways of working. Experience with production software or digital manufacturing systems such as SAP, MES, or similar platforms. A proactive attitude with a high level of ownership, accountability, and attention to detail. Good communication skills in English. Willingness to work a rotating 3-shift or 5-shift schedule. Other Information: This is an excellent opportunity to join a global biotechnology leader and work in a highly automated, GMP-regulated manufacturing environment. You'll benefit from competitive compensation, career development opportunities, and a collaborative, innovative workplace while contributing to the production of life-changing medicines for patients worldwide. If you are interested and would like to apply, please submit your application via the apply button below or contact me for more information

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

About the Company Our client is a global biotechnology leader dedicated to improving patients' lives through innovative medicines. Operating advanced, highly automated manufacturing facilities, the company is committed to quality, safety, innovation, and continuous improvement while offering excellent opportunities for professional growth. Role Description As an Equipment Operator, you will operate and optimize automated production and packaging equipment, troubleshoot technical issues, perform minor maintenance, and support continuous improvement initiatives. Working in a GMP-regulated environment, you will help ensure safe, efficient, and reliable manufacturing while contributing to operational excellence and product quality. Responsibilities - Manage and oversee automated production and packaging lines, ensuring safe and efficient operations. - Perform equipment setup, product changeovers, line clearances, and routine cleaning activities. - Diagnose and resolve technical issues to minimize downtime and optimize equipment performance. - Carry out minor maintenance tasks and machine adjustments to support operational reliability. - Record production activities and performance data using SAP and MES. - Support deviation investigations, root cause analysis (RCA), and continuous improvement initiatives. - Ensure compliance with GMP, quality, safety, and operational standards. Requirements - Experience operating automated production, assembly, packaging, or process equipment in a manufacturing environment. - Strong technical troubleshooting, analytical, and problem-solving skills. - Experience with Root Cause Analysis (RCA), 5 Why, or other structured problem-solving methodologies. - Familiarity with GMP-regulated environments and manufacturing systems such as SAP and MES. - A proactive mindset with a strong focus on safety, quality, continuous improvement, and operational excellence. - Ability to work independently as well as collaboratively in a fast-paced production environment. - Good communication skills in English and willingness to work in rotating 3-shift or 5-shift schedules. Other Information If you are interested and would like to apply, please submit your application using the Apply button below or contact me for more information.

The Company  A leading global biotechnology organization, dedicated to developing and delivering innovative medicines to improve patient outcomes. Operating worldwide, the company combines science, technology, and quality-driven processes to ensure safe and effective clinical products.   Role Description We are seeking a skilled Automated Production Systems Technician to support the operation and optimization of advanced, automated manufacturing lines. The role involves ensuring production runs smoothly, adhering to GMP standards, and contributing to process improvements within a regulated environment. Responsibilities -Operate and oversee automated production equipment following SOPs and GMP requirements. -Troubleshoot issues and conduct root cause analysis to resolve technical problems. -Adjust mechanical and process parameters to maximize machine performance. -Record, verify, and manage production data in SAP/MES systems accurately. -Monitor process performance, identify deviations, and escalate when necessary. -Prepare accurate GMP documentation, including batch records and logs. -Participate in problem solving sessions with QA, Engineering, and Production teams. -Carry out equipment setup and shutdown procedures. Requirements -Minimum of 3 years’ experience in a similar production or manufacturing role, ideally in assembly and packaging. -Proven experience working with automated production systems. Fluency in English. -Comfortable working in a structured environment with strict procedures. -Willingness to work in shifts and commute as required. -Ability to participate in triage and problem-solving sessions involving QA, Maintenance, and Production. -Capable of documenting activities following GMP standards. Other Information If you are interested and want to apply, please submit your application via the apply button below and contact me.

Over het bedrijf Sluit je aan bij een toonaangevende internationale farmaceutische producent waar geneesmiddelen worden geëtiketteerd, geassembleerd, opgeslagen en wereldwijd gedistribueerd. Je werkt in een hoog geautomatiseerde GMP-productieomgeving en draagt bij aan een betrouwbare productie, continue verbetering en operationele excellentie. Functieomschrijving Als Technical Operator – Geautomatiseerde Productielijnen ben je verantwoordelijk voor het bedienen, bewaken en optimaliseren van volledig geautomatiseerde productielijnen. Je zorgt ervoor dat het productieproces veilig, efficiënt en volgens de geldende kwaliteits- en GMP-richtlijnen verloopt. Daarnaast speel je een belangrijke rol bij het oplossen van technische storingen, het verbeteren van de prestaties van de apparatuur en het waarborgen van een hoge productkwaliteit binnen een gereguleerde productieomgeving. Verantwoordelijkheden Bedienen en bewaken van volledig geautomatiseerde productie- en verpakkingslijnen. Uitvoeren van machine-instellingen, omstellingen, line clearance-werkzaamheden en reinigingsactiviteiten. Oplossen van storingen aan apparatuur en productieprocessen met behulp van gestructureerde probleemoplossingsmethodieken. Uitvoeren van klein technisch onderhoud en mechanische of parametertechnische afstellingen. Vastleggen van productieactiviteiten en batchgegevens in SAP- en MES-systemen. Ondersteunen bij afwijkingsonderzoeken (deviation investigations) en productiegerelateerde triageactiviteiten. Uitvoeren van Root Cause Analyses (RCA, 5 Why) en implementeren van corrigerende maatregelen. Actief bijdragen aan Lean- en Continuous Improvement-initiatieven. Waarborgen van naleving van GMP-, veiligheids- en kwaliteitsrichtlijnen. Bijdragen aan optimale prestaties van de productielijnen en een efficiënte productie. Functie-eisen Afgeronde MBO-opleiding in een technische richting of een vergelijkbaar opleidingsniveau. Ervaring met het bedienen van volledig geautomatiseerde productie-, assemblage-, etiketteer- of verpakkingslijnen. Sterke analytische vaardigheden en ervaring met het oplossen van technische storingen. Ervaring met Root Cause Analysis (RCA), 5 Why of vergelijkbare probleemoplossingsmethodieken. Ervaring binnen een gereguleerde productieomgeving; ervaring met GMP is een sterke pré. Ervaring met SAP en/of MES-systemen. Kennis van Lean Manufacturing of Continuous Improvement is een pré. Proactieve, kwaliteitsgerichte werkhouding en in staat om zelfstandig te werken. Goede beheersing van de Engelse taal. Bereidheid om te werken in een 3-ploegendienst, met de mogelijkheid om in de toekomst over te gaan naar een 5-ploegendienst. Arbeidsvoorwaarden Fulltime functie. Aantrekkelijke ploegentoeslagen en goede arbeidsvoorwaarden. Uitgebreide opleidings- en ontwikkelmogelijkheden. Moderne productieomgeving met veel aandacht voor veiligheid, kwaliteit en het welzijn van medewerkers.

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 Automated Production Line Technician (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.