Today, Lonza is a global leader in life sciences operating across five continents. While we work in science, there’s no magic formula to how we do it. Our greatest scientific solution is talented people working together, devising ideas that help businesses to help people. In exchange, we let our people own their careers. Their ideas, big and small, genuinely improve the world. And that’s the kind of work we want to be part of.
Are you prepared to join an exceptional team at Lonza AG and make a meaningful impact in the field of life sciences? As a QC Associate based in Geleen, Netherlands, you will play a vital role in ensuring the impeccable quality of our products. This is an outstanding opportunity to be part of an exceptionally ambitious team, working on groundbreaking projects and advancing your career in a dynamic environment.

KEY REQUIREMENTS:

• BSc/MSc or equivalent experience in Life Sciences, Biotechnology, Biochemistry, Cell Biology, or Microbiology.
• Prior experience in GMP/Quality Control is a plus.
• Intermediate or higher vocational education in chemistry/biotechnology.
• Preferably, experience with analytical techniques such as RT-qPCR, HPLC, ELISA, and LC-MS.
• Strong communication skills in English.
• Demonstrated accuracy, tidiness, self-organization, flexibility, and attention to detail.
• A great teammate with a detailed and responsible working attitude.
  At Lonza, we are dedicated to encouraging an inclusive and collaborative culture where every team member can thrive. If you are determined to compete at the highest level and successfully implement innovative solutions, we want you on our team!
  Every day, Lonza’s products and services have a positive impact on millions of people. For us, this is not only a great privilege, but also a great responsibility. How we achieve our business results is just as important as the achievements themselves. At Lonza, we respect and protect our people and our environment. Any success we achieve is no success at all if not achieved ethically.
  People come to Lonza for the challenge and creativity of solving complex problems and developing new ideas in life sciences. In return, we offer the satisfaction that comes with improving lives all around the world. The satisfaction that comes with making a meaningful difference

• Plan and complete daily quality control testing activities while strictly following GMP and safety standards.
• Perform and review analytical tests such as qPCR, HPLC, ELISA, endotoxin, and cell count in accordance with the defined training program.
• Guarantee the accurate functioning of laboratory equipment and assist in the execution of QC methods during the transition of QC assays and stability testing.
• Cooperate cross-departmentally to ensure timely processing and reporting of results.
• Report test results to the Supervisor QC and initiate Quality Events such as NC’s, CRF’s, and OOS’s.
• Perform intermediate testing and release of Drug Products, growing your experience across several QC assays and projects.