Vacature QC Associate

QC Associate in Geleen

As a QC Associate, you play a key role in ensuring that materials and products meet strict quality standards before they are used or released. You work hands-on in the lab, performing tests that directly contribute to the production of life-saving therapies.

You are part of a close-knit QC team where reliability, accuracy and collaboration are essential. Together, you ensure that results are delivered on time and meet the highest standards, enabling the next steps in the manufacturing process.

This is a practical, lab-focused role where you continuously develop your technical skills, work according to GMP standards, and build experience across a variety of QC methods.

What you will get

• A hands-on laboratory role with direct impact on product quality and patient safety
• The opportunity to learn and work with a wide range of QC techniques (e.g. qPCR, ELISA, Flow Cytometry)
• A structured environment where you build GMP and quality expertise
• A supportive team where you can grow, take ownership and develop your skills
• A dynamic role with variation across projects, assays and daily activities
• Shift work that comes with additional compensation and flexibility in your schedule
  
  

What you will do

• Perform QC assays such as qPCR, Flow Cytometry, ELISA, endotoxin and cell-based tests
• Accurately document and review test results in line with GMP requirements
• Support the release of materials and products by delivering reliable and timely results
• Write and review documentation such as SOPs, protocols and quality instructions
• Maintain laboratory equipment and ensure proper operation
• Support method transfers, stability testing and continuous improvement activities
• Initiate and support quality events such as deviations, OOS and change requests
• Collaborate with QC and other departments to ensure smooth and timely processes
  
  

What we are looking for

• MBO or HBO degree in biotechnology, chemistry or a related field
• Interest in working in a laboratory and following quality-driven processes (GMP)
• Any hands-on lab experience (e.g. from education or internships) is a plus
• A precise, structured and responsible way of working
• Strong attention to detail and commitment to quality
• Good communication skills in English
• This role requires working in a shift pattern
  
  

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.

Innovation thrives when people from all backgrounds bring their unique perspectives to the table. At Lonza, we are committed to creating an inclusive environment where everyone can contribute and grow.

Ready to make an impact in quality control within life sciences? Apply now