Research Associate III

Research Associate III (Cell Therapy Development)

Geleen, Netherlands
 

As a Research Associate III, you play a key role in supporting cell therapy process development by executing laboratory activities and ensuring the lab operates efficiently within a cGMP environment. This is a hands-on role where you combine technical expertise with a strong sense of ownership to keep processes running reliably and in compliance with quality standards.
 

What you will get

• A hands-on, lab-driven role where you are central to daily operations
• Real ownership in maintaining and improving lab processes within a cGMP environment
• Exposure to a broad range of cell therapy techniques and technologies
• Close collaboration with scientists and cross-functional teams (QC, QA, R&T)
• A stable environment for people who enjoy operational excellence over constant change
• The opportunity to build deep technical expertise and become a go-to person in the lab
   

What you will do

• Execute and support laboratory experiments for cell therapy process development in a cGMP environment
• Ensure smooth day-to-day lab operations, including preparation, execution and follow-up of experiments
• Perform cellular, biochemical and molecular techniques such as cell culture, qPCR/RT-PCR, flow cytometry, ELISA and microscopy
• Maintain accurate and compliant documentation in line with GMP requirements
• Analyse experimental data and support preparation of reports and summaries for internal and client discussions
• Support process transfer, method optimization and collaboration with QC, QA and R&T
• Maintain lab readiness by managing materials, reagents and general lab upkeep
   

What we are looking for

• Master’s degree with at least 2 years of experience, or Bachelor’s degree with 4+ years of relevant laboratory experience
• Hands-on experience with cell culture (iPSCs, hMSCs, primary cells preferred)
• Experience working in a GMP or regulated environment is strongly preferred
• Familiarity with analytical and cell-based techniques (e.g. qPCR, flow cytometry, ELISA)
• Strong attention to detail and documentation skills, structured and reliable way of working, with a focus on quality
• A proactive team player who takes ownership of lab activities
   

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.