GMP Validation & Document Control Engineer
Verista, Inc.
Verista, Inc. seeks a Validation Engineer to own document and data control for the C&Q team, including repository structure, ValGenesis routing, turnover documentation, review/approval tracking, executed record quality, and closeout readiness. The role involves building document trackers, coordinating templates and approvals, and maintaining dashboards while ensuring GMP standards and electronic records compliance. On-site in Devens, MA with full-time commitment. #J-18808-Ljbffr Verista, Inc.
Vacancy posted 1 day ago
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