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QC Associate
full-timeGeleen

Summary

Location

Geleen

Type

full-time

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About this role

 

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, supporting the testing and release of materials, products and utilities used in manufacturing. As a QC Associate, you will plan and perform daily quality assays and control activities, ensuring all work meets GMP and safety standards. This is a hands-on laboratory role with variety, responsibility and room to grow.

What you will get

  • A practical QC laboratory role in a GMP-regulated environment.

  • The opportunity to work with a range of assays across multiple projects.

  • A supportive team with training, guidance and development opportunities.

  • A varied role that offers flexibility and continuous learning.

What you will do

  • Perform and review cell-based and microbiological assays such as qPCR, FLOW, ELISA, endotoxin and cell count.

  • Write and review QC documentation, including SOPs, work instructions and protocols.

  • Ensure laboratory equipment is used correctly and remains operational.

  • Support method transfer activities and stability testing.

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

  • Report test results and issues to the QC Team Leader.

  • Initiate Quality Events such as deviations, change requests and OOS investigations.

What we are looking for

  • A careful and responsible working attitude with strong attention to detail.

  • Willingness to work in a rotating shift system, including nights and weekends.

  • Preferably experience with GMP and basic QC techniques (microbiology, EM or analytical assays).

  • Good communication skills in English.

  • Organized, flexible and able to manage changing priorities.

  • A team player who enjoys working in a collaborative environment.

  • Laboratory education or relevant lab experience in chemistry, biotechnology or a related field

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.

Other facts

Tech stack
Attention To Detail,GMP,Microbiology,Analytical Assays,Communication Skills,Organizational Skills,Flexibility,Team Player

About Lonza

Lonza is a pioneer and world leader in the CDMO industry, setting the pace with cutting-edge science, smart technology, and lean manufacturing. United by a common purpose, we turn our customers’ breakthrough innovations into viable therapies and manufacture the medicines of tomorrow.

Founded in Switzerland in 1897, our company is the first and original CDMO, and today we are more dynamic, agile and forward-focused than ever before. As one of the largest Western CDMOs, we bring together a global team of around 18,500 colleagues across five continents to deliver comprehensive, integrated solutions for our customers' complex needs.

For our customers and their patients, we bring quality, safety and reliability to bring life-enhancing and life-saving treatments to market at speed and at scale. For our colleagues, we strive to create a sense of belonging and inclusion where every person can thrive and bring their best.

Team size: 10,001+ employees
LinkedIn: Visit
Industry: Pharmaceutical Manufacturing
Founding Year: 1897

What you'll do

  • As a QC Associate, you will perform and review various quality assays and control activities, ensuring compliance with GMP and safety standards. You will also support method transfer activities and collaborate with other departments for timely testing and reporting.

Ready to join Lonza?

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Frequently Asked Questions

What does a QC Associate do at Lonza?

As a QC Associate at Lonza, you will: as a QC Associate, you will perform and review various quality assays and control activities, ensuring compliance with GMP and safety standards. You will also support method transfer activities and collaborate with other departments for timely testing and reporting..

Why join Lonza as a QC Associate?

Lonza is a leading Pharmaceutical Manufacturing company.

Is the QC Associate position at Lonza remote?

The QC Associate position at Lonza is based in Geleen, Limburg, Netherlands. Contact the company through Clera for specific work arrangement details.

How do I apply for the QC Associate position at Lonza?

You can apply for the QC Associate position at Lonza directly through Clera. Click the "Apply Now" button above to start your application. Clera's AI-powered platform will help match your profile with this opportunity and guide you through the application process. You can also learn more about Lonza on their website.