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 Responsibilities Draft 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). Requirements 46 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).