Job Title

We are currently looking for a Cleaning Validation Consultant with mid-level experience to support urgent validation activities at our clients manufacturing site in Guelph. The project follows a recent FDA audit and requires immediate support for protocol drafting and execution of cleaning validations across multiple equipment.This is a hands-on role for consultants who are flexible, proactive, and comfortable working on-site, including nights and weekends as needed.Key ResponsibilitiesDraft and review Cleaning Validation Protocols in accordance with cGMP and FDA expectations.Execute cleaning validation activities for a variety of equipment and manufacturing systems.Collaborate closely with QA, Validation, and Operations teams to ensure proper documentation and alignment with regulatory standards.Support documentation practices and conformance reviews.Be available for on-site activities, including outside of regular working hours (24/7 operation site).Requirements46 years of experience in Cleaning Validation in a GMP-regulated environment.Demonstrated ability to write clear and compliant Validation Protocols and reports.Knowledge of Current Good Manufacturing Practices (cGMP) and FDA requirements.Availability to be on-site in Guelph regularly.Willingness to work night shifts or weekends if needed.Fluent in English (spoken and written).