Lonza is seeking a Senior Validation Engineer in Vacaville, California. This fully site-based role involves executing validation activities for manufacturing processes and ensuring compliance with regulatory standards. The ideal candidate will have a bachelor's degree in engineering or a related field and 5-8 years of experience in validation within the pharmaceutical or biotechnology industry.Key responsibilities include oversight of commissioning and qualification processes, developing validation protocols, and providing technical leadership across project teams. A strong understanding of cGMP and FDA regulations is essential.#J-18808-Ljbffr