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Validation Engineer

Pfizer
September 10, 2026
Full-time
On-site
Wisconsin, United States
Operations
Role: Validation professional supporting qualification, validation, and compliance activities in a regulated manufacturing environment. Responsibilities: evaluate and review protocols, troubleshoot validation issues, write technical reports, contribute to validation projects, and ensure adherence to cGMP and industry standards. Requirements: bachelor's degree with relevant experience, or associate's degree with 4+ years, or high school diploma with 6+ years' experience; strong understanding of FDA regulations, GxP, and validation principles; proficiency in data analysis tools like Excel; excellent communication and organizational skills. Preferred: technical writing experience, equipment qualification knowledge, collaborative skills, adaptability, and familiarity with AI tools for problem solving. High-value specifics: manufacturing environment with focus on equipment and process validation, cGMP compliance, and cross-functional collaboration. Work setup: on-premise with potential off-hours work; physical demands include manufacturing area presence and safety compliance.