The CSV Engineer validates GxP computerized systems at an undisclosed client site, ensuring compliance with 21 CFR Part 11, EU Annex 11, and GAMP 5. The role supports gene therapy manufacturing by leading validation activities for systems such as Veeva QMS, BMRAM, and analytical laboratory instruments; the posting excerpt is truncated and does not provide location, compensation, education, experience, benefits, work arrangement, or employment type.
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