Process Manager Biopharma GMP Environment | Prozessmanager Biopharma GMP-Bereich (m,w,d)

Job Summary

This role involves supporting a pharmaceutical industry client in Marburg, focusing heavily on cross-departmental deviation management, technical deviations, calibration deviations, and process deviations within a highly regulated GMP environment. The Process Manager will also contribute expert input to various project teams focused on investment, yield optimization, product quality, viral safety, and capacity expansion. Key activities include critically analyzing production processes, equipment usage, and process flows to identify optimization opportunities, drafting complex change requests, coordinating their implementation across multiple departments, and ensuring compliance through validation and qualification. Candidates must possess a scientific degree, ideally in biotechnology, and demonstrate initial experience in deviation handling and protein purification within a GMP-regulated setting, coupled with fluent German and English skills.