Reporting to the Manager Validation, the Validation Engineer II supports the qualification/validation programs for equipment, instruments, and facility used in cellular manufacturing at Charles River Laboratories. As a technical resource for GMP regulated facilities, the Validation Engineer II assists primarily in the development and execution of verification/qualification/validation protocols of cell therapy manufacturing systems, ensuring equipment and facility are operating in compliance with Charles River Laboratories and all applicable regulatory requirements. The Validation Engineer II is expected to work cooperatively with Manufacturing, Facilities, Materials Management, Quality Assurance, and other departments as necessary.