Lonza Group→
QC Associate at Lonza Group in Geleen, Limburg, The Netherlands
Entry LevelOn-siteFull-timeGeleen, Limburg, The Netherlands
Job Description
QC Associate
Location: NL - Geleen
QC Associate
Geleen, The Netherlands
As a QC Associate, you are responsible for performing quality control activities that support the release of manufacturing areas, incoming materials, utilities and products. Depending on the assigned area of responsibility, activities may focus on Cell Therapy, Environmental Monitoring or Raw Materials within a GMP-regulated environment.
What you will get
A diverse QC role with exposure to multiple laboratory and quality processes
The opportunity to build experience within Cell & Gene Therapy and GMP-regulated operations
Hands-on experience with microbiological, analytical and/or cell-based testing techniques
Cross-functional collaboration with Manufacturing, Supply Chain and Quality teams
A dynamic laboratory environment where quality, accuracy and teamwork are essential
What you will do
Perform routine QC activities and laboratory assays in support of product release and GMP operations
Execute environmental monitoring, microbiological, analytical or cell-based testing activities depending on the assigned QC area
Perform sampling activities for cleanrooms, utilities and/or incoming materials
Document, review and report test results in line with GMP and data integrity standards
Support laboratory equipment handling, sample management and shipment coordination where applicable
Collaborate cross-functionally to ensure timely processing, testing and release activities
Initiate and support quality events such as deviations, investigations, OOS or related GMP records
What we are looking for
MBO, HBO, Bsc or Msc in Biotechnology, Microbiology, Life Sciences, Biomedical Sciences or another laboratory-related discipline
Hands-on laboratory experience through work, internships or educational projects
Affinity with QC testing, microbiology, environmental monitoring, cell-based assays or analytical techniques
GMP knowledge or experience is considered a strong plus
Accurate and structured way of working with strong attention to detail
Good communication skills in English and ability to work collaboratively within a team
Motivated to work in a fast-paced and highly regulated GMP environment
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.
Ready to shape the future of life sciences? Apply now.