Location
stalden (vs)
Job Type
Full-time
Posted
June 19, 2026
Job Description
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