Job Summary Ideal candidate must be: - proficient in MS Word and MS Excel with good overall computer literacy - be meticulous and detail-oriented to comply with the expectations of a GxP-oriented quality system - have an MSc in an applicable field with experience in the following: o Biosafety cabinet / aseptic technique o Wet-laboratory experience o Advantageous experience includes: - Cell culture experience (human / mammalian) - Flow cytometry - Genetic modification of human / mammalian cells - Molecular biology techniques The post will entail: - Full-time on-site position - Overtime as and when required, including weekends - On-call hours split between members of the department - Working in a GxP cleanroom facility - Haematopoietic progenitor cell cryopreservation, thawing, and infusion - Donor lymphocyte cryopreservation, thawing, and infusion - Manufacturing of genetically modified cell and gene therapy products (CAR T cells) - Patient interaction - Document preparation - SOP writing - Validation writing and execution - Data management, handling, and analysis o Processing of data into publications / posters / presentations - Interaction with government agencies / regulators e.g. permit applications - Stock and equipment management Applicants should note the following: - Minimum of 3 references are required - Position to start on Monday 1 September 2025 CLOSING DATE: 20/07/2025 AT 17H00