Description
The role performs downstream biopharmaceutical production activities, including purification, filtration, chromatography, concentration, equipment operation and cleaning, campaign preparation, in-process checks, sampling, GMP documentation, and support for deviations, CAPA, and equipment and process qualification and validation. It requires a biology, chemistry, pharmaceutical, or comparable laboratory or technical qualification, GMP experience, downstream-processing knowledge, German and English language skills, shift availability, and a quality-oriented team approach.
