
This entry-level Validation Engineer role supports quality control laboratory operations within the pharmaceutical industry. The position focuses on executing equipment qualification activities to ensure compliance with cGMP regulations and corporate quality standards. Key responsibilities include authoring and executing qualification protocols, coordinating with laboratory personnel and vendors, and identifying compliance gaps to drive continuous improvement. The role offers a structured work environment with a clear path for potential conversion to a full-time position. Candidates will work onsite in Vacaville, California, on a standard weekday schedule, contributing to a team dedicated to maintaining operational integrity and patient safety.










