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Freelance Cleaning & CSV Documentation Specialist – Pharmaceutical Manufacturing 📍 Strasbourg, France – 5 Days Onsite 📅 6–12 Month Contract – ASAP Start I’m currently supporting a pharmaceutical organisation looking for an experienced Cleaning & CSV Documentation Specialist to support a new equipment project at their manufacturing site in Strasbourg. The consultant will represent the user side from a Cleaning perspective, taking responsibility for preparing the required documentation for new equipment, ensuring CSV requirements are met and supporting the development and maintenance of the Operational Handbook. 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 activities associated with the introduction of new equipment, • Work cross-functionally with Cleaning, Validation, Quality and wider project stakeholders, • Ensure documentation is accurate, compliant and maintained throughout the project Key Requirements: • Strong experience within pharmaceutical/biopharmaceutical manufacturing, • Previous Cleaning/Cleaning Validation experience within a GMP environment, • Experience with Computerized System Validation (CSV) requirements, • Strong GMP documentation experience, • Experience supporting new equipment projects within pharmaceutical manufacturing, • Strong cross-functional communication and stakeholder management skills, • French speaking required, • Available to work 5 days per week onsite in Strasbourg If you have relevant Cleaning, CSV and pharmaceutical manufacturing experience and are available for a new freelance project, please get in touch!

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