5+ Years Job Description The Cleaning Validation Engineer will report to the Cleaning Validation Senior Manager and support laboratory and manufacturing cleaning validation activities for new and existing products and equipment in a cGMP biopharmaceutical manufacturing environment Key Responsibilities Support cleaning validation activities for laboratory and manufacturing equipment. Perform TOC swab and rinse sampling. Conduct cleanability studies and degradation studies. Support CIP (Clean-in-Place) cycle development studies for new equipment. Troubleshoot cleaning validation and CIP-related issues. Perform TFF (Tangential Flow Filtration) sanitization activities. Author and peer-review cleaning validation protocols, reports, investigations, and related documentation. Ensure cleaning validation activities comply with cGMP requirements. Required Qualifications At least 5 years of direct experience or close familiarity with general cleaning validation practices in a cGMP biopharmaceutical manufacturing environment. Knowledge of cleaning validation procedures and practices. Familiarity with TOC swab and rinse sampling. Understanding of cleanability studies, degradation studies, and CIP cycle development. Ability to prepare and review validation protocols, reports, and investigations. Preferred Qualifications Experience troubleshooting CIP cycles. Experience with LabWare and Veeva. #