In this position, you will help shape analytical strategies, coordinate method development and validation, and ensure the reliable release of biopharmaceutical drug substances across multiple German sites. This role is fixed‑term until december 2027, offering you a valuable opportunity to advance your career in a dynamic, fast‑growing CDMO environment while contributing directly to the development and manufacturing of cutting‑edge biopharmaceuticals. Join our analytical management team in our Quality Control department in Hamburg.
