Analytical Scientist

Make your mark for patientsAnalytical ScientistWe are looking for an Analytical Scientist who is curious, detail-oriented, and collaborative to join our Analytical Development Sciences team, based at our UCB campus located in Braine-l'Alleud, Wallonia, Belgium.About the roleThe primary goal of the function is the development, qualification, and validation of robust and efficient Physico-chemical methods (Liquid Chromatography, Electrophoresis capillary), validation of those methods to the required regulatory requirement standards, and the transfer of these tests to internal or external laboratories , from early clinical phases to commercialThe candidate will also provide analytical support and expertise to process and product understanding/characterization and will be responsible for generating data and preparing regulatory submissions with business partners.The position will later transition in the Gene Therapy QC Testing team with the following scope and responsibilities:• implementing high throughput analytical tools supporting the release and stability of multiple therapeutic gene therapy programs throughout clinical phases (from phase 1 to readiness to launch).• Supporting the development, validation, tech transfer (to internal or external partners) and execute fast and reliable assays to support the clinical development of AAV-based Gene Therapy Products• Supporting process development activities by executing reliable and QC friendly analytical methods (ELISA, qPCR/dPCR, Liquid chromatography).Who you will work withYou will join a dynamic and multicultural team within the PCA group, collaborating closely with QC, research, and external partners. As you transition to the Gene Therapy QC Testing team, you will continue to work cross-functionally with internal and external stakeholders to ensure analytical excellence across UCB’s gene therapy pipeline.What you will do· Manage and perform daily laboratory activities related to physico-chemical method development, validation, and transfers; support routine testing (GT in-process, release, stability).· Analyze results, verify data, and provide analytical expertise to projects; present and discuss findings in project team meetings.· Prepare, review, and approve documentation including procedures, protocols, and reports.· Contribute to the implementation of new technologies and continuous improvement initiatives.· Ensure all activities are conducted in a GMP-regulated environment, aligned with regulatory and quality standards.· Collaborate cross-functionally with internal teams and support knowledge sharing and operational excellence.Interested?· Bachelor’s degree or higher with relevant experience in analytical techniques for biologicals or chemicals in a bio/pharma company and GMP-regulated lab.· Expertise in analytical techniques such as liquid chromatography and capillary electrophoresis; experience in molecular biology techniques (qPCR, dPCR, ELISA) is a plus.· Strong lab skills and autonomy in method development/validation; ability to write and review accurate GMP/GSP documentation in English.· Solid understanding of regulatory requirements and GMP rules; capable of managing multiple priorities and providing leadership.· Excellent interpersonal skills and proven experience as a scientist, ideally in the biotech/pharma industry.Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you