Biologist | Biologe (m/w/d)

Job Summary

This role involves overseeing development projects for finished pharmaceutical products from market launch throughout their entire lifecycle, working within interdisciplinary teams. Key responsibilities include managing complaints, deviations, and change requests, as well as creating, reviewing, and maintaining quality documentation such as MBRs, PQRs, Risk Assessments, and stability programs. The successful candidate will coordinate all quality-related matters concerning finished products with manufacturing partners' Quality Units and clients, and present Quality processes during customer audits, regulatory inspections, and internal audits. The position requires a strong background in natural sciences or engineering, extensive experience in pharmaceutical manufacturing, and excellent knowledge of GxP and ICH guidelines. This is an attractive opportunity for a professional who thrives in a dynamic, team-oriented environment with flat hierarchies and a focus on continuous development.