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 get
- An agile career and dynamic working culture
- An inclusive and ethical workplace where your ideas are valued
- Compensation programs that recognize high performance
- A comprehensive range of benefits based on your role and location
- Opportunities to develop your technical expertise in GMP manufacturing and advanced therapy production
- A collaborative team environment focused on continuous improvement.
What you will do
- Performing 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 identity
- Performing final product commercial packing and shipping activities and samples shipments following good distribution practices and GMP compliance
- Completion and review of GMP documentation ensuring
- Use of GMP systems daily to complete activities
- Use 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 activities
- Maintain clean, organized, and safe work areas while promptly reporting deviations, quality concerns, or safety issues to supervisors.
- Technical 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 collaborative, adaptable, and proactive approach with a commitment to safety, quality, and continuous learning.
At Lonza, our people are our greatest strength. With 30\+ sites across five continents, our globally connected teams work together every day to manufacture the medicines of tomorrow. Our core values of Collaboration, Accountability, Excellence, Passion and Integrity reflect who we are and how we work together. Everyone's ideas, big or small, have the potential to improve millions of lives, and that's the kind of work we want you to be part of.
Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we value diversity and are committed to creating an inclusive environment for all employees. If you're ready to help turn our customers' breakthrough ideas into viable therapies, we look forward to welcoming you on board.
Ready to shape the future of life sciences? Apply now!
Deze vacature komt van Indeed. Originele vacature bekijken ↗