Senior QC Associate

Job Title: Senior QC Associate
Location: Geleen
12 Month Fixed Term Contract

We are looking for a Senior QC Associate to join our company, you will perform testing of the product in accordance with approved procedures with quality or safety standards, and will be involved in sampling, and in-process sample and products.

Responsible for planning and execution of routine assays and quality control activities while ensuring compliance with all existing GMP and safety standards in the area of responsibility.

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

• Hands-on experience in a QC laboratory or related role within the pharmaceutical, biotechnology, or similar industry.
• Extensive practical and technical knowledge of analytical methods and laboratory techniques (e.g., qPCR, Sequencing, HPLC, LC-MS, ELISA)
• Plan, execute and review quality control analytical tests, including: In-process control (IPC) and DS/ DP product testing and stability studies.
• Write, review, and maintain quality documentation (SOPs, protocols, reports, and quality instructions).
• Draft and review method validation protocols and reports in line with regulatory guidelines. Participate in execution of method validation activities.
• Initiate and participate in quality events (deviations, investigations, OOS, CAPA). Identify risks and gaps in processes and contribute to implementation of improvements.
• Collaborate cross-functionally to ensure timely processing and reporting of results.

What we are looking for

• This position requires hands-on experience in analytical laboratory techniques in a biotechnological environment.
• The position requires a positive responsible working attitude and GMP mind .
• Intermediate or higher vocational education in chemistry/biotechnology.
• Extensive experience with GMP and good knowledge of analytical (RT-qPCR, UV-Spec, ELISA, HPLC, LC-MS) techniques including compendial methods.
• Good communication skills in English.
• Accuracy, tidiness, self-organized, flexible, attention to detail.

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.