Logistics Associate – Warehouse
Lonza is looking for new staff to join its growing GMP Warehouse and Logistics team!As a world leading contract development and manufacturing organisation (CDMO) Lonza is looking to people with a passion to help others and committed to delivering excellence for our customers patients. Our mission is to bring life changing medicines to patients and that requires a strong team with a passion for quality and excellence.If you are looking for a dynamic job where you can proudly make a difference for patient lives, take a look at our Warehouse and Logistics job openings to join our growing team at Lonza Netherlands. As a Warehouse and Logistics associate we handle the supply chain. From incoming goods receipt and storage and final product shipments, supporting our production teams to make life changing medicine.This is a fully site-based role. Working together in person supports close, real-time collaboration and the technical precision needed to manufacture medicines to the highest quality and safety standards. This role is on a rotating shift including days and night and weekends more details available. What you will getAn agile career and dynamic working cultureAn inclusive and ethical workplace where your ideas are valuedCompensation programs that recognize high performanceA comprehensive range of benefits based on your role and locationOpportunities to develop your technical expertise in GMP manufacturing and advanced therapy productionA collaborative team environment focused on continuous improvement.The full list of our global benefits can be found here: Employee Benefits | Lonza What you will doPerforming activities related to goods receipt, labelling, storage and general inventory management within a validated GMP inventory management system (SAP)Incoming patient material handling and receipt (Apheresis/Leukopak/etc.) and ensuring accurate record of chain of identityPerforming final product commercial packing and shipping activities and samples shipments following good distribution practices and GMP complianceCompletion and review of GMP documentation ensuringUse of GMP systems daily to complete activitiesUse and maintenance of equipment such as large gas supplies, lift trucks and dry shippers etc.Working with a dynamic site with opportunities for cross functional activitiesMaintain clean, organized, and safe work areas while promptly reporting deviations, quality concerns, or safety issues to supervisors. What we are looking forTechnical education or equivalent experience, preferably with a background in science or logistics.Entry-level experience (0–4 years) in manufacturing, science, logistics, or a related environment.Business-level English communication skills, both written and verbal.Ability to work effectively in a GMP-regulated manufacturing environment.Strong organizational skills, attention to detail, and the ability to prioritize routine and repetitive tasks while maintaining quality.A collaborativ...