Key Responsibilities

• Consulting operations regarding cleaning validation analytics for existing projects, NPI and growth projects
• Responsibility for the organization of cleaning studies in QC
• Setup QC plans in LIMS for cleaning validation and cleaning samples
• Review of analyses for cleaning samples
• Participation in and responsibility for audits and inspections
• On-call duty every 3-4 months (assignments are carried out remotely)

Key Requirements

• Experience in the pharmaceutical industry in the field of cleaning validation is an advantage
• GMP experience is an advantage
• You enjoy taking on challenges in a dynamic environment
• You have a very good understanding of German and English