About this role
Are you passionate about biotechnology and eager to contribute to life-changing therapies? Join Lonza in Geleen as a Biotech Associate and become part of a global leader in life sciences. In this hands-on manufacturing role, you will work in a GMP cleanroom environment, helping to produce advanced cell therapy products that have a direct impact on patients' lives. At Lonza, innovation starts with people. We empower our employees to develop their careers, share ideas, and make meaningful contributions to the future of healthcare. Wie zoeken we? What we are looking for: Completed laboratory training, vocational education or a bachelor's degree in biotechnology, biology or a related field. Ideally 2 years of experience working in a GMP cleanroom environment. Strong attention to detail and a quality-focused mindset. Ability to follow procedures accurately and work in a structured manner. Good communication skills and a collaborative approach to teamwork. Good English communication skills, both written and verbal. Willingness to work in a shift pattern, including evenings and weekends. A valid driver's license is required due to limited public transport availability during shift hours. Wat bieden wij je? We offer: A hands-on position in a state-of-the-art GMP manufacturing environment. The opportunity to work with cutting-edge cell therapy technologies. Comprehensive training and career development opportunities. A collaborative, supportive, and inclusive workplace culture. A strong focus on quality, innovation, and continuous improvement. Competitive salary and performance-based recognition programs. Directly a contract by Lonza Attractive benefits package tailored to role and location. Annual base salary: €32,250 - €45,150 gross per year, depending on experience, qualifications, and expected contribution. Functieomschrijving As a Biotech Associate, you will play a key role in the manufacturing of advanced therapy medicinal products while ensuring the highest standard of quality and compliance: What you will do: 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 while following strict aseptic techniques. Complete production documentation accurately and on time. Identify and report deviations to help ensure compliance and product quality. Support continuous improvement initiatives within the manufacturing team. Collaborate with QA, QC and MSAT teams to support efficient manufacturing operations. Working in 5 shifts, 2 morningshifts, 2 afternoon shifts, 2 nightshifts.