Qualification and Validation Specialist (Biotech/Pharma) | Qualifizierung | Validierung | Biotechnik-/Pharma (m/w/d)

Job Summary

This role involves supporting management and production teams in the planning, documentation, and execution of qualification and validation projects within a GMP-regulated pharmaceutical environment. You will act as the primary point of contact for relevant interfaces, balancing administrative desk work with hands-on activities at production facilities. Key responsibilities include creating GMP-compliant documentation, managing routine organizational tasks, and overseeing sub-projects related to process and cleaning validation. The position is ideal for a proactive professional who enjoys independent project management and cross-departmental collaboration. Joining this independent family-owned company offers a stable environment with flat hierarchies, comprehensive social benefits under the chemical industry collective agreement, and a strong focus on professional development and work-life balance through flexible working hours.