About the Company Join a leading international pharmaceutical manufacturer where medicines are labeled, assembled, stored, and distributed worldwide. Working in a highly automated GMP manufacturing environment, you’ll help ensure reliable production while contributing to continuous improvement and operational excellence. Role Description As a Technical Operator – Automated Lines, you will operate, monitor, and optimize fully automated production equipment to ensure safe, efficient, and compliant manufacturing. You will play an important role in troubleshooting technical issues, improving equipment performance, and maintaining high quality standards within a regulated production environment. Key Responsibilities Operate and monitor fully automated production and packaging lines Perform machine set-ups, changeovers, line clearances, and cleaning activities Troubleshoot equipment and process issues using structured problem-solving methods Perform minor maintenance and mechanical or parameter adjustments Record production activities and batch data in SAP and MES systems Support deviation investigations and production triage activities Perform Root Cause Analyses (RCA, 5 Why) and implement corrective actions Contribute to Lean and Continuous Improvement initiatives Ensure compliance with GMP, safety, and quality requirements Support optimal equipment performance and production efficiency Requirements MBO degree or…

The Company A leading global biotechnology organization operating in a highly regulated GMP environment, focused on high-quality manufacturing, compliance, and continuous improvement. Role Overview We are seeking a Technical Operator (Automated Lines) to operate and optimize highly automated production systems, ensuring efficient, compliant, and high-quality manufacturing. The role combines technical expertise with operational discipline to maintain equipment performance and support continuous improvement. Key Responsibilities – Operate and monitor automated production equipment according to SOPs and GMP standards. – Perform troubleshooting, root cause analysis, and machine parameter adjustments. – Maintain accurate GMP documentation and production data in SAP/MES systems. – Perform equipment set-up, close-down, and cleaning activities. – Participate in triage and problem-solving with QA, M&E, and Production teams. – Support Lean and continuous improvement initiatives and ensure effective shift handovers. Requirements – Minimum 3 years of experience in a similar production role, preferably in assembly and packaging. – Proven experience in an automated production environment, preferably pharmaceutical or food manufacturing. – Technical education such as MBO / VAPRO B or equivalent. – Strong knowledge of GMP, SOPs, SAP/MES, and manufacturing…

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…

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.…

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…

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,…