GMP Cell Therapy Manufacturing Associate

Lonza Group; Netherlands; Remote; EUR 32,000 - 45,000; Full time

Job summary

Lonza in Geleen, Netherlands, is seeking a Biotech Associate to contribute to the manufacturing of advanced cell therapy products in a GMP cleanroom. This hands-on role requires precision, teamwork and a strong quality mindset to bring life-changing therapies to patients.

You will perform cell culture, media preparation, expansion and harvesting in a regulated environment, document production accurately, report deviations, and collaborate with QA, QC and MSAT to improve operations.

Qualifications

• Bachelor's degree in biotechnology or related field required.
• Ideally 2 years of GMP cleanroom experience.
• Strong attention to detail and quality mindset.
• Ability to follow procedures accurately and work in a structured manner.
• Good English communication skills (written and verbal).
• Willingness to work in shift pattern (evenings/weekends).
• A valid driver’s license due to limited public transport during shift hours.

Responsibilities

• Perform cell and tissue culture activities according to GMP procedures.
• Execute manufacturing steps such as media preparation, cell expansion and harvesting.
• Work in a cleanroom environment following strict aseptic techniques.
• Complete production documentation accurately and on time.
• Identify and report deviations to ensure compliance and product quality.
• Support continuous improvement initiatives within the manufacturing team.
• Collaborate with QA, QC and MSAT teams to support efficient operations.

Skills

Attention to detail

Teamwork

English communication

Communication

Structured work style

Education

Bachelor's degree in biotechnology

Job description

Lonza in Geleen, Netherlands, is seeking a Biotech Associate to contribute to the manufacturing of advanced cell therapy products in a GMP cleanroom. This hands-on role requires precision, teamwork and a strong quality mindset to bring life-changing therapies to patients.

You will perform cell culture, media preparation, expansion and harvesting in a regulated environment, document production accurately, report deviations, and collaborate with QA, QC and MSAT to improve operations.