Compliance

• Contribution to the development of optimized qualification and validation concepts
• Execution of qualifications for high‑tech equipment in the pharmaceutical and biopharmaceutical industry
• Participation in risk analyses
• Support in validation projects (e.g., cleaning, process, and method validations)
• Preparation of GMP‑compliant documentation, including Standard Operating Procedures (SOPs)
• Review of technical documents and drawings, as well as changes and deviations

Consultant GMP Compliance, Quality Assurance

Consultant, Project Manager GMP Compliance