Laboratory Technician - Cell Culture

Your next challenge Ready to make a difference? Here’s what awaits you. As a Laboratory Technician – Cell Culture, you will play a key role in supporting the bioassays that drive the development of innovative therapies. By ensuring cell culture operations and reliable analytical preparation, you will directly contribute to the advancement of medicines that may one day change lives. You will join a team of 5–6 dedicated colleagues, led by the Technical Leader Bioassays, working together to accelerate safe access to innovative treatments. Your key responsibilities Here’s what you’ll take ownership of: Performing cell passages to support a range of bioassays Processing analytical data to ensure reliable and well-documented results Drafting clear and accurate analysis reports Preparing reagents, solutions and buffers required for assays Skills you’ll need to bring To succeed in this role, you’ll bring: Scientific background equivalent to BAC+2 or BAC+3 Solid knowledge of cell amplification processes Strong organisational skills and attention to detail Ability to adapt to a role involving various laboratory tasks Initiative and sense of responsibility Team-focused working style English level equivalent to B1 Experience in a similar role in the pharmaceutical industry, GMP/BPF settings or regulatory frameworks (HACCP, ISO) Our commitment to you Joining us means growing in an environment where scientific excellence goes hand-in-hand with human values. In this role, you will: Develop your expertise in cell culture within a supportive and experienced team Contribute to a portfolio of bioassay projects for international partners Benefit from continuous development through our new internal training space, the “Pharma Academy” Work with cutting-edge technologies thanks to our reinvestment strategy Enjoy a collaborative atmosphere that supports work-life balance and personal well-being  Who we are (and why it matters) Quality Assistance is a CRO focused on analytical sciences for innovative medicine development. Based in Belgium and GxP-certified, we provide EMA- and FDA-compliant services from a single-site facility equipped with a comprehensive range of state-of-the-art technologies. With over 40 years of experience and 280 professionals, we have contributed to the development of more than 2,000 drug candidates. We continue to expand while remaining firmly rooted in scientific excellence, operational rigor, and regulatory reliability.