Description
The role develops, validates, and transfers analytical methods for pharmaceutical products, with a focus on GC-MS and supporting LC-MS/MS, LC-qTOF-MS, and HPLC-PDA techniques. Responsibilities include lifecycle management, impurity and leachables/extractables quantification, study planning, reporting, OOX investigations, deviations, CAPA processes, and laboratory compliance. Candidates need a natural-sciences degree or relevant apprenticeship, GxP experience, mass-spectrometric analytical knowledge, German and English proficiency, and strong communication and teamwork skills.
