Associate Director CMC Manufacturing Technologies | Pharmacist (m/w/d)

Job Summary

This role is for an experienced Associate Director to join a global CMC team in Mainz, Germany, focusing on raw materials and excipients for individualized RNA therapeutics. The successful candidate will be responsible for overseeing phase-appropriate material requirements, authoring gap assessments, and managing Quality by Design (QbD) documents like Critical Material Attributes (CMA) and Critical Quality Attributes (CQA) templates. This position involves significant collaboration with internal and external teams to ensure compliance through all clinical phases, supporting CMC teams, and driving continuous process improvement for material assessment and procurement. The role is a temporary 18-month parental leave replacement, offering a chance to contribute to cutting-edge biopharmaceutical manufacturing.