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Lonza

QC Associate I

Reposted Yesterday
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In-Office
Geleen
Entry level
In-Office
Geleen
Entry level
As a QC Associate, you will test materials and products, maintain compliance, assist with method execution, and support laboratory operations in a 24/7 setting.
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QC Associate

Geleen, Netherlands

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.

Based in Geleen, you will work as part of our Quality Control team to support testing of materials, in-process samples, products and cleanroom environments. This is a hands-on laboratory role in a 24/7 shift environment, which means you will also rotate through shifts as part of your regular schedule. You will contribute to QC testing, laboratory operations and GMP compliance across one of several QC specializations, including Operations, Environmental Monitoring, Microbiology, Raw Materials or Support.

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
  • Perform testing on incoming materials, in-process samples, environmental samples and final products.

  • Follow GMP, data integrity and ALCOA+ principles in all QC activities.

  • Support the execution and transfer of QC methods, including routine and stability testing.

  • Maintain laboratory documentation, logbooks and equipment in a compliant state.

  • Assist with instrument maintenance, calibration and basic troubleshooting.

  • Work with other departments to ensure timely reporting and processing of results.

  • Participate in Quality Events such as deviations, investigations and CAPAs.

  • Work in rotating shifts as part of a continuous 24/7 QC operation.

What we are looking for
  • Completed laboratory training or relevant lab experience. A bachelor’s degree in a scientific field is also welcome.

  • Preferably experience with GMP or QC techniques such as EM sampling, microbiological tests or analytical assays.

  • Strong attention to detail with a precise and responsible working attitude.

  • Good communication skills in English, both written and verbal.

  • Organized, accurate and flexible, with the ability to manage changing priorities.

  • A team-oriented mindset and willingness to support colleagues across QC.

  • Interest in learning new assays, instruments and QC processes.

  • Willingness and ability to work in a 24/7 shift system.

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.

Lonza is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a qualified individual with disability, protected veteran status, or any other characteristic protected by law.

Top Skills

Alcoa+
Analytical Assays
Gmp
Microbiological Tests

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