Job Description

Job Title: QC Lab Facilitator
Location: Geleen
12 Month Fixed Term Contract

We are looking for a detailed orientated and enthusiastic QC Lab Facilitator to join our company and the ideal candidate will have interest in management of quality control lab activities, equipment maintenance, material ordering and management, KANBAN, LIMS (Laboratory Information Management System) project management, technical writing, and shipments.

What you will get

• A varied laboratory role with the opportunity to grow skills across several QC disciplines.
• Hands-on experience with a wide range of assays, techniques and GMP processes.
• A supportive team environment with training, coaching and clear development pathways.
• The chance to contribute directly to the quality and safety of life-changing therapies.

What you will do

• Management of laboratory equipment; vendor visits, periodic qualification reviews,
• Lighthouse data monitoring, downloading data and reviewing for compliance according to procedures
• Management of stocks of chemicals and lab items: Creating Procurement Requests, receiving materials, reagents and standards, storage and maintenance of KANBAN
• Receiving retention and reference samples, and managing storage
• Organizing the storage areas and housekeeping management.
• Perform calibrations activities, e.g. balance calibration, help clean glassware, rinse showers and eyewash;
• Prepare documentation as needed, including issue forms, SOPs, revisions

What we are looking for

• Hands on experience (5+ years) in QC laboratory or related role within the pharmaceutical, biotechnology, or similar industry.
• Bachelor's degree in a relevant scientific field (e.g., chemistry, biology, or related discipline).
• Minimum of 2 years of experience in a QC or related role within the pharmaceutical, biotechnology, or similar industry under GMP regulations.
• Proficiency in LIMS, SAP software and experience with master data creation and modification.
• Good communication skills in English.
• Knowledge of regulatory requirements (e.g., FDA, cGMP, ICH guidelines).

About Lonza

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.