Process Engineer - Life Science (all genders)

You plan, design, and optimize pharmaceutical and biotechnological production processes. You carry out scale-up and tech transfer projects from development to routine production. You create process flow diagrams, risk analyses, and technical specifications (P&ID, URS, FAT/SAT). You support qualification and validation activities (DQ, IQ, OQ, PQ) in accordance with GMP guidelines. You evaluate and implement new technologies to increase efficiency and automation. You work closely with internal departments such as quality, production, maintenance, and engineering. You create and maintain GMP documentation, SOPs, and batch records. You have a degree in process engineering, biotechnology, chemical engineering, or pharmaceutical engineering. You have experience in pharmaceutical or biotechnological production—ideally in a GMP-regulated environment. You bring knowledge in process planning, control, and validation. You have relevant professional experience in a regulated environment (pharma, biotech, or medtech). You work in a team-oriented, goal-driven manner with a high level of commitment. You have business-fluent command of German and English in spoken and written form. We value diversity and therefore welcome all applications—regardless of gender, nationality, ethnic and social origin, religion/worldview, disability, age, and sexual orientation and identity.