Biopharma Upstream Processing Specialist | Mitarbeiter*in Biopharma Upstream Processing (USP) (m,w,d)

Job Summary

This role involves supporting biopharmaceutical production within an Upstream Processing (USP) environment for a 1.5-year fixed-term contract. The successful candidate will perform GMP-compliant in-process control (IPC) analytics, such as measuring pH, osmolality, cell count, and viability. Key responsibilities include managing inoculum activities, cell cultivation, and maintaining rigorous GMP-compliant documentation in both paper and electronic formats. The specialist will also oversee specific IPC and inoculum equipment, including calibration and maintenance, while contributing to deviation management and SOP development. This position is ideal for a professional with a strong background in biotechnology or bioengineering who thrives in a highly regulated GMP environment, values quality standards, and enjoys mentoring new team members. You will work closely with cross-functional USP teams to ensure production efficiency and process improvement.