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QC Laboratory Administrator

Lonza -
Verviers

Soumettre votre candidature

Détails de l'emploi

Temps plein
De 31 500 € à 44 100 € par an

Qualifications

Français

Description complète du poste

QC Laboratory Administrator

Location: Verviers – laboratory‑based role

We are looking for a QC Laboratory Administrator to support the quality release of raw materials, finished products and shelf‑life studies. In this role, you will play a key part in ensuring testing, documentation and data flow run smoothly to support safe and timely product release.

https://www.youtube.com/watch?v=wZaXzPKWEv0&list=PLh3u2rKfWyIfXC2d2O3enUrpMjjJ7DO_x&index=18

The full‑time annual base pay for this position in Belgium is expected to range between €31,500 and €44,100. Initial salary placement within this range will be determined based on role‑related factors such as experience, qualifications, and expected contribution.

What you will get

An agile career and dynamic working culture.
An inclusive and ethical workplace where your contribution matters.
Compensation programmes that recognise high performance.
A variety of benefits dependent on role and location.
The full list of our global benefits can be found here: https://www.lonza.com/careers/benefits

What you will do

Receive and check samples for compliance, then prepare and dispatch them for required testing.
Coordinate testing with chemistry, microbiology and external laboratories as needed.
Request external testing quotes, prepare shipments and track sample progress.
Review test results and documentation to support QC release of materials and products.
Ensure test requests, batch documentation and system data are aligned and complete.
Maintain accurate records in SAP and local tracking tools.
Support team priorities by contributing to meetings and resolving documentation issues promptly.

What we are looking for

A higher education qualification in chemistry, biology, biochemistry or a related discipline.
Experience working in a Quality Control or regulated laboratory environment.
Understanding of ISO and cGMP principles within pharma, biotech or chemical industries.
Fluency in French, with a good working knowledge of English.

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. If you’re ready to help turn our customers’ breakthrough ideas into viable therapies, we look forward to welcoming you on board.

Ready to shape the future of life sciences? Apply now.

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