Description
The role supports cellular drug manufacturing for tumor and monogenic disease therapies by creating GMP documentation, performing occasional quality-control analyses, developing electronic workflows, and validating computer-assisted systems. The position also contributes to process optimization, quality standards, and GMP compliance. Candidates should have BTA, MTA, CTA, PTA, or a natural-science bachelor’s degree, ideally GMP quality-control experience and knowledge of flow cytometry, qPCR, visual inspection, microbiological testing, and endotoxin assays, along with strong software aptitude and English communication skills. The role offers flexible scheduling, mobile working, training, and other benefits.
