CQV Validation Engineer - GMP Clinical Manufacturing
20BLOC
20BLOC is seeking a motivated Validation Engineer to support clinical manufacturing readiness for GMP facility systems at the Thousand Oaks site. You will generate, review, and execute CQV documentation, including IQ/OQ/PQ protocols, and coordinate with engineering, manufacturing, quality, and vendors. This role emphasizes hands-on field execution and documentation under supervision. Ideal candidates have 0–5 years of CQV or GMP experience, strong technical writing, and familiarity with FDA 21 #J-18808-Ljbffr 20BLOC
Vacancy posted 1 day ago
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