Scientific Associate Quality Control – Pharmacy / CDMO | Wissenschaftlicher Mitarbeiter Qualitätskontrolle – Pharmazie / CDMO (m/w/d)

Job Summary

This role involves ensuring the quality of diagnostic raw materials, intermediate, and finished products within a growing international company focused on radiopharmaceutical medicines. The Scientific Associate will be responsible for analytical testing, developing and maintaining analytical methods like HPLC and UV/Vis spectroscopy, and creating essential documentation such as SOPs and specifications. The position also includes participating in stability studies, method validation, analytical transfers, and audits, as well as communicating with clients and CDMO partners. This is an attractive opportunity for a detail-oriented professional with a scientific background and experience in instrumental analytics, especially HPLC, to contribute to a future-proof industry with a focus on nuclear medicine.