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Previous Cleaning/Cleaning Validation experience within a GMP environment. If you have relevant Cleaning, CSV and pharmaceutical manufacturing experience and are available for a new freelance project, please get in touch!. Freelance Cleaning & CSV Documentation Specialist – Pharmaceutical Manufact

Key Responsibilities: - Prepare user documentation related to new manufacturing equipment from the Cleaning department perspective - Ensure documentation meets relevant Computerized System Validation (CSV) requirements - Develop and maintain the Operational Handbook - Support documentation activitie